CO替代物参与羰基化反应研究进展

doi:10.6023/cjoc202412012

摘要/Abstract

羰基化反应产物中的“羰基”官能团通常来源于气体一氧化碳(CO)或者其替代物. 气体CO作“羰源”虽然底物普适性广泛, 可实现工业化放大生产, 但其本身有毒且易燃; CO替代物的化学性质稳定且容易获得, 反应过程易于操作且分离后处理简单. 因此, 借助CO替代物实现羰基化转化, 为构建多种化学品提供了一系列强大且前景广阔的工具. 总结和讨论了使用CO替代物(二氧化碳、氯仿、羧酸及羧酸衍生物、羰基金属试剂、酰氯类化合物等)作为羰源合成高附加值化学品的最新进展, 展望了不同羰源在羰基化反应中的发展前景以及存在的难点, 以期为推动研制更多新型的CO替代物提供借鉴.

关键词: 羰基化反应, 一氧化碳替代物, 二氧化碳, 氯仿, 羧酸衍生物, 羰基金属试剂, 酰氯

The “carbonyl” functional group of the products in carbonylation reactions usually comes from gas carbon monoxide (CO) or its surrogates. Although gas CO as carbonyl source has wider substrate scope and can achieve industrial production, it is toxic and flammable. CO surrogates have stable chemical properties, which are easy to obtain. The reaction process is easy to operate and the separation/post-treatment is simple. Therefore, CO surrogates provide a variety of powerful and promising tools for the carbonylative conversion and construction of diverse chemicals. This review summarizes and discusses the latest progress in synthesizing high value-added chemicals using CO surrogates (carbon dioxide, chloroform, carboxylic acids and their derivatives, carbonyl metal reagents, acyl chlorides, etc.) as carbonyl sources. Finally, the development prospects and existing difficulties of different carbonyl sources in carbonylation reactions were discussed, in order to provide reference for promoting the development of more novel CO surrogates.

Key words: carbonylation, CO surrogates, carbon dioxide, chloroform, carboxylic acid derivatives, carbonyl metal reagent, acyl chloride

引用此文

冯保林, 王鹏, 赵德明, 杨桂爱, 晏耀宗, 史会兵, 王耀伟. CO替代物参与羰基化反应研究进展[J]. 有机化学, 2025, 45(8): 2773-2795.

Baolin Feng, Peng Wang, Deming Zhao, Guiai Yang, Yaozong Yan, Huibing Shi, Yaowei Wang. Research Progress on CO Surrogates in Carbonylation Reactions[J]. Chinese Journal of Organic Chemistry, 2025, 45(8): 2773-2795.

导出引用 EndNote|Reference Manager|ProCite|BibTeX|RefWorks

分享此文

图/表 57

图式1. 应用于羰基化反应中的CO替代物

Scheme 1. CO surrogates used in carbonylation reactions

图式2. 钯催化芳基溴与CO2的直接羧化反应

Scheme 2. Palladium-catalyzed direct carboxylation of aryl bromides with CO2

图式3. 室温条件下氟化物催化CO2高效转化为CO

Scheme 3. Efficient fluoride-catalyzed conversion of CO2 to CO at room temperature

图式4. 高效钌催化胺、H2和CO2的N-甲酰化反应

Scheme 4. Highly efficient Ru-catalyzed N-formylation of amines with H2 and CO2

图式5. 可见光驱动苯乙烯、CO2和芳基卤化物的还原碳芳基化反应

Scheme 5. Visible-light-driven reductive carboarylation of styrenes with CO2 and aryl halides

图式6. 钯催化烷基碘或烯烃的硫羰基化反应

Scheme 6. Pd-catalyzed thiocarbonylation of alkyl iodides or alkenes

图式7. CO2和氢硅烷参与分子内Heck羰基化反应实现烯烃的碳羧化过程

Scheme 7. Carbo-carboxylation of alkenes via intramolecular Heck carbonylation utilizing CO2 and hydrosilane

图式8. CO2高效活化与选择性转化

Scheme 8. Efficient activation and selective conversion of CO2

图式9. 以CO2为CO替代物合成酮的电催化串联反应

Scheme 9. Electrocatalytic cascade reaction for the synthesis of ketones using CO2 as CO surrogate

图式10. 芳基炔烃与CO2的电化学E-选择性半还原二羧基化反应

Scheme 10. Electrochemical E-selective semireductive dicarboxylation of aryl alkynes with CO2

图式11. 氯仿和碱参与的钯催化有机卤代物的羰基化反应

Scheme 11. Palladium-catalyzed carbonylation of organic halides by chloroform and alkali

图式12. 钯催化卤代7-氮杂吲哚和其他杂芳烃的氨羰基化反应

Scheme 12. Palladium-catalyzed aminocarbonylation of halo- substituted 7-azaindoles and other heteroarenes

图式13. 钯催化Heck环化反应以及原位氢羧化反应

Scheme 13. Pd-catalyzed Heck cyclization and in situ hydrocarboxylation

图式14. 钯催化芳基卤化物对NH-亚砜肟亚胺的芳酰基化反应

Scheme 14. Palladium catalyzed aroylation of NH-sulfoximines with aryl halides

图式15. 钯催化的羰化偶联反应合成芳基酮和芳基酯

Scheme 15. Palladium catalyzed carbonylative coupling for synthesis of arylketones and arylesters

图式16. 钯催化2-酰胺基咪唑并[1,2-a]吡啶的合成

Scheme 16. Pd-catalyzed synthesis of 2-amidoimidazo[1,2- a]pyridines

图式17. Pd/C催化氯仿作为CO源的尿素衍生物的串联合成

Scheme 17. Pd/C-catalyzed domino synthesis of urea derivatives using chloroform as CO source

图式18. 氯仿为CO替代物参与钯催化末端炔烃与胺的羰基化制备α,β-烷基酰胺

Scheme 18. Direct access to α,β-alkynylamides via Pd-catalyzed carbonylation of terminal alkynes with amines using chloroform as the CO surrogate

图式19. 配体调控钯催化芳基卤化物和甲酸选择性合成醛和羧酸化合物

Scheme 19. Palladium-catalyzed ligand-controlled selective synthesis of aldehydes and acids from aryl halides and formic acid

图式20. 硅烷羧酸作为高效释放CO的分子: 合成及其在钯催化羰基化反应中的应用

Scheme 20. Silacarboxylic acids as efficient CO releasing molecules: synthesis and application in Pd-catalyzed carbonylation reactions

图式21. 有机光还原催化和过渡金属催化的氢甲酰化反应

Scheme 21. Organo-photoredox catalyzed and transition-metal catalyzed hydroformylation

图式22. 草酸原位生成CO参与钯催化芳基卤化物的羰化酯化反应

Scheme 22. Oxalic acid as the in situ CO generator in Pd-cata- lyzed hydroxycarbonylation of arylhalides

图式23. 钯催化烯烃与草酸的区域选择性氢羧化反应

Scheme 23. Pd-catalyzed regiodivergent hydrocarboxylation of olefins with oxalic acid

图式24. 可见光驱动烷基卤化物的有机催化羰基化反应

Scheme 24. Organocatalyzed carbonylation of alkyl halides driven by visible light

图式25. 碱促进炔丙基胺的羰基化环化反应

Scheme 25. Base-promoted carbonylative cyclization of propargylic amines

图式26. 钯催化炔丙基二醇与伯胺羰基化合成羧酸

Scheme 26. Pd-catalyzed carbonylation of propargyl diols with primary amines for the synthesis of acids

图式27. 钯催化乙酸酐和甲酸根阴离子对芳基和乙烯基卤化物或三氟甲烷的羰基化反应

Scheme 27. Pd-catalyzed hydroxycarbonylation of aryl and vinyl halides or triflates by acetic anhydride and formate anions

图式28. 钯催化芳基、烯基和烯丙基卤代物与甲酸苯酯的羰基化反应

Scheme 28. Pd-catalyzed carbonylation of aryl, alkenyl, and allyl halides with phenyl formate

图式29. 钯催化烯基甲苯磺酸酯羰基化制备α,β-不饱和酯和酰胺

Scheme 29. Preparation of α,β-unsaturated esters and amides via Pd-catalyzed carbonylation of alkenyl tosylates

图式30. 甲酸三氯苯酯作为CO替代物: 钯催化芳基/烯基卤化物和三氟甲烷的羰基化反应

Scheme 30. Trichlorophenyl formate as CO surrogate: Pd-catalyzed carbonylation of aryl/alkenyl halides and triflates

图式31. 钯催化甲酸酯Heck环化/羰基化: 氮杂吲哚-3-乙酸酯和呋喃氮杂吲哚的合成

Scheme 31. Pd-catalyzed Heck cyclization/carbonylation with formates: synthesis of azaindoline-3-acetates and furoazaindolines

图式32. 以N-羟基琥珀酰亚胺甲酸酯为CO替代物的钯催化芳基、烯基和烯丙基卤代物的羰基化反应

Scheme 32. Pd-catalyzed carbonylation of (hetero)aryl, alkenyl and allyl halides by means of N-hydroxysuccinimidyl formate as CO surrogate

图式33. 草酸二乙酯作为CO源的钯催化溴代和氯代芳烃的乙氧羰基化反应

Scheme 33. Diethyloxalate as CO source for Pd-catalyzed ethoxycarbonylation of bromo- and chloroarene derivatives

图式34. 温和条件下可见光驱动烯烃、甲酸盐和CO2的二羧化反应

Scheme 34. Visible-light-driven alkene dicarboxylation with formate and CO2 under mild conditions

图式35. 空气下微波加热胺的氨羰基化反应

Scheme 35. Amines in microwave-heated aminocarbonylation reactions under air

图式36. Co2(CO)8作为CO源用于(杂)芳基卤化物与高度失活的(杂)芳香胺的氨羰基化反应

Scheme 36. Co2(CO)8 as CO source for the amino carbonylation of (hetero)aryl halides with highly deactivated (hetero)arylamines

图式37. 以羰基钴为CO源参与(杂)芳基卤化物和三氟甲烷的还原羰基化反应

Scheme 37. Reductive carbonylation of (hetero) aryl halides and triflates using cobalt carbonyl as CO source

图式38. 光驱动芳基卤化物的三组分羰基化反应

Scheme 38. Light-driven three-component carbonylation of aryl halides

图式39. 去芳香性羰基化反应

Scheme 39. Dearomative carbonylations

图式40. 酰氯参与钌催化芳香C—H键的羰基化反应

Scheme 40. Ru-catalyzed carbonylation of aromatic C—H bonds using acid chloride

图式41. 锌介导草酰氯还原生成CO及其在羰基化反应中的应用

Scheme 41. Zn-mediated reduction of oxalyl chloride forming CO and its application in carbonylations

图式42. CO的原位生成及其在钯催化氨羰基化反应中的应用

Scheme 42. Generation of CO and its efficient incorporation in Pd-catalyzed aminocarbonylations

图式43. 镍催化烯烃还原芳基化制备含羰基的恶吲哚类化合物

Scheme 43. Ni-catalyzed reductive arylacylation of alkenes toward carbonyl-containing oxindoles

图式44. 原位生成CO参与钯催化芳基(类)卤化物的氯羰基化反应

Scheme 44. Pd-catalyzed chlorocarbonylation of aryl (pseudo)halides through in-situ generation of CO

图式45. 以草酰氯为羰源的镍催化高选择性还原羰基化反应

Scheme 45. Ni-catalyzed highly selective reductive carbonylation using oxalyl chloride as the carbonyl source

图式46. 以草酰氯为羰源、镍催化三氟甲磺酸乙烯酯与烷基溴的羰化偶联反应合成烯酮

Scheme 46. Nickel-catalyzed carbonylative coupling of vinyl triflates with alkyl bromides toward enones with oxalyl chloride as the carbonyl source

图式47. 醇作为钌催化氢酯化反应的CO/H2源

Scheme 47. Alcohols as CO/H2 sources in Ru-catalyzed hydroesterification

图式48. 利用甘油作为Pd催化苯乙烯烷氧羰基化反应中的CO源

Scheme 48. Utilizing glycerol as CO-source in Pd-catalyzed alkoxycarbonylation of styrenes

图式49. 铑催化醛类化合物参与的Pauson-Khand反应

Scheme 49. Rh-catalyzed Pauson-Khand-type reaction with aldehydes

图式50. 铑配合物催化烯烃与多聚甲醛的氢甲酰化反应

Scheme 50. Hydroformylation of olefins with paraformaldehyde catalyzed by Rh complexes

图式51. 无CO参与的芳基和烯基碘化物的氨羰基化反应

Scheme 51. CO-free aminocarbonylation of aryl and alkenyl iodides

图式52. 钯催化N-甲酰糖精和芳基卤化物的羰基化反应

Scheme 52. Pd-catalyzed carbonylation of aryl halides with N-formylsaccharin as a CO Source

图式53. 以N-甲酰糖精为CO源的钯催化氟羰基化反应

Scheme 53. Pd-catalyzed fluorocarbonylation using N-formyl- saccharin as CO source

图式54. 铜催化吲哚和六酮环己烷的羰基化反应

Scheme 54. Copper-catalyzed carbonylative transformations of indoles with hexaketocyclohexane

图式55. 使用二噁唑酮作为羰基化试剂的2-烯基/吡咯基苯胺的无金属C—H [5＋1]羰基化反应

Scheme 55. Metal-free C—H [5＋1] carbonylation of 2-alkenyl/pyrrolylanilines using dioxazolones as carbonylating reagents

图式56. 光活化CO供体参与光介导的钯催化羰基化反应

Scheme 56. Light-activated CO donor for Pd-catalyzed and light-mediated carbonylation

图式57. 钯催化二氟卡宾转移引发碘代苯和末端炔烃歧化合成γ-丁烯和炔酮

Scheme 57. Pd-catalyzed difluorocarbene transfer enabled divergent synthesis of γ-butenolides and ynones from iodobenzene and terminal alkynes

参考文献 242

[1]	Peng, J. B.; Wu, F. P.; Wu, X. F. Chem. Rev. 2019, 119, 2090.
[2]	Cao, Y. W.; He, L. Synlett 2022, 33, 1003.
[3]	Ye, B. H.; Su, L.; Zheng, K. T.; Gao, S.; Liu, J. W. Angew. Chem., Int. Ed. 2024, 63, e202413949.
[4]	Wu, X. F.; Neumann, H.; Beller, M. Chem. Rev. 2013, 113, 1.
[5]	An, D. L.; Bao, Z. P.; Wu, X. F. Chin. J. Org. Chem. 2023, 43, 2304 (in Chinese).
	(安大列, 包志鹏, 吴小锋, 有机化学, 2023, 43, 2304.) doi: 10.6023/cjoc202301010
[6]	Herrera, M. V.; Domke, L.; Börner, A. ACS Catal. 2014, 4, 1706.
[7]	Wang, P.; Yang, D.; Liu, H. Chin. J. Org. Chem. 2021, 41, 3448 (in Chinese).
	(王鹏, 杨妲, 刘欢, 有机化学, 2021, 41, 3448.)
[8]	Shi, H. B.; Wang, Y. W.; Wang, P.; Zhao, D. M.; Feng, B. L.; Yan, Y. Z.; Yang, G. A. Chin. J. Org. Chem. 2024, 44, 1811 (in Chinese).
	(史会兵, 王耀伟, 王鹏, 赵德明, 冯保林, 晏耀宗, 杨桂爱, 有机化学, 2024, 44, 1811.) doi: 10.6023/cjoc202301025
[9]	Chen, X. Z.; Chen, G.; Lian, Z. Chin. J. Chem. 2024, 42, 177.
[10]	Cao, Y. W.; Yang, J. G.; Deng, Y.; Wang, S. C.; Liu, Q.; Shen, C. R.; Lu, W.; Che, C. M.; Chen, Y.; He, L. Angew. Chem., Int. Ed. 2020, 59, 2080.
[11]	Morimoto, T.; Kakiuchi, K. Angew. Chem., Int. Ed. 2004, 43, 5580.
[12]	Boehm, P.; Denton, E. H.; Wick, J.; Morandi, B. J. Org. Chem. 2023, 88, 5069.
[13]	Hirschbeck, V.; Gehrtz, P. H.; Fleischer, I. J. Am. Chem. Soc. 2016, 138, 16794. doi: 10.1021/jacs.6b11020 pmid: 27966917
[14]	Gatlik, B.; Chaładaj, W. ACS Catal. 2021, 11, 6547.
[15]	Yin, Z. P.; Wang, Z. C.; Wu, X. F. Chin. J. Org. Chem. 2019, 39, 573 (in Chinese).
	(尹志平, 王泽超, 吴小锋, 有机化学, 2019, 39, 573.) doi: 10.6023/cjoc201809004
[16]	Cao, J.; Zheng, Z. J.; Xu, Z.; Xu, L. W. Coord. Chem. Rev. 2017, 336, 43.
[17]	Sang, R.; Schneider, C.; Razzaq, R.; Neumann, H.; Jackstell, R.; Beller, M. Org. Chem. Front. 2020, 7, 3681.
[18]	Gautam, P.; Bhanage, B. M. Catal. Sci. Technol. 2015, 5, 4663.
[19]	Chen, Z. K.; Wang, L. C.; Wu, X. F. Chem. Commun. 2020, 56, 6016.
[20]	Rao, K.; Sharma, A.; Rathod, G.; Barahdia, A. S.; Jain, R. Org. Biomol. Chem. 2025, 23, 980.
[21]	Börjesson, M.; Moragas, T.; Gallego, D.; Martin, R. ACS Catal. 2016, 6, 6739. pmid: 27747133
[22]	Hua, K.; Liu, X.; Wei, B.; Zhang, S.; Wang, H.; Sun, Y. Acta Phys. -Chim. Sin. 2021, 37, 2009098.
[23]	Ye, J. H.; Ju, T.; Huang, H.; Liao, L. L.; Yu, D. G. Acc. Chem. Res. 2021, 54, 2518.
[24]	Ju, T.; Zhou, Y. Q.; Cao, K. G.; Fu, Q.; Ye, J. H.; Sun, G. Q.; Liu, X. F.; Chen, L.; Liao, L. L.; Yu, D. G. Nat. Catal. 2021, 4, 304.
[25]	Yan, T.; Chen, X.; Kumari, L.; Lin, J.; Li, M.; Fan, Q.; Chi, H.; Meyer, T. J.; Zhang, S.; Ma, X. Chem. Rev. 2023, 123, 10530.
[26]	Li, D.; Wei, L.; Qi, C.; Xiong, W.; Liu, H.; Jiang, H. J. Org. Chem. 2023, 88, 5205.
[27]	Li, D.; Wei, L.; Xiong, W.; Jiang, H.; Qi, C. J. Org. Chem. 2023, 88, 5231.
[28]	Ren, X.; Zheng, Z.; Zhang, L.; Wang, Z.; Xia, C.; Ding, K. Angew. Chem., Int. Ed. 2017, 56, 310.
[29]	Wang, L.; Sun, W.; Liu, C. Chin. J. Chem. 2018, 36, 353.
[30]	Guo, Y.; Wei, L.; Jiang, H.; Qi, C. Asian J. Org. Chem. 2024, 13, e202400142.
[31]	Correa, A.; Martín, R. J. Am. Chem. Soc. 2009, 131, 15974.
[32]	Lescot, C.; Nielsen, D. U.; Makarov, I. S.; Lindhardt, A. T.; Daasbjerg, K.; Skrydstrup, T. J. Am. Chem. Soc. 2014, 136, 6142.
[33]	Wu, Y.; Luo, J.; Huang, Y. Prog. Chem. 2022, 34, 1431 (in Chinese).
	(吴亚娟, 罗静雯, 黄永吉, 化学进展, 2022, 34, 1431.) doi: 10.7536/PC210909
[34]	Zhang, L.; Han, Z. B.; Zhao, X. Y.; Wang, Z.; Ding, K. L. Angew. Chem., Int. Ed. 2015, 54, 6186.
[35]	Yatham, V. R.; Shen, Y.; Martin, R. Angew. Chem., Int. Ed. 2017, 56, 10915.
[36]	Ye, J. H.; Miao, M.; Huang, H.; Yan, S. S.; Yin, Z. B.; Zhou, W. J.; Yu, D. G. Angew. Chem., Int. Ed. 2017, 56, 15416.
[37]	Hou, J.; Ee, A.; Cao, H.; Ong, H. W.; Xu, J. H.; Wu, J. Angew. Chem., Int. Ed. 2018, 57, 17220.
[38]	Fu, Q.; Bo, Z. Y.; Ye, J. H.; Ju, T.; Huang, H.; Liao, L. L.; Yu, D. G. Nat. Commun. 2019, 10, 3592.
[39]	Gao, Y.; Cai, Z.; Li, S.; Li, G. Org. Lett. 2019, 21, 3663.
[40]	Wang, H.; Li, Y. D.; Sun, Y. J.; Li, Y. H. J. Org. Chem. 2023, 88, 8835.
[41]	Wang, H.; Li, C.; Li, Y. D.; Chen, J. B.; Liu, S. L.; Li, Y. H. Org. Chem. Front. 2024, 11, 1322.
[42]	Shi, Q.; Li, Y.; Li, Y.; Dong, Y.; Liu, S.; Li, Z.; He, L.; Sun, L.; Li, Y. J. Catal. 2025, 442, 115870.
[43]	Li, Y.; Dong, Y.; Wei, Z.; Yan, C.; Li, Z.; He, L.; Li, Y. Chin. Chem. Lett. 2024, 35, 110206.
[44]	Yan, F.; Bai, J. F.; Dong, Y.; Liu, S.; Li, C.; Du, C. X.; Li, Y. JACS Au 2022, 2, 2522.
[45]	Dong, Y.; Yang, P.; Zhao, S.; Li, Y. Nat. Commun. 2020, 11, 4096.
[46]	Wang, H.; Dong, Y.; Zheng, C.; Sandoval, C. A.; Wang, X.; Makha, M.; Li, Y. Chem 2018, 4, 2883.
[47]	Lian, Z.; Nielsen, D. U.; Lindhardt, A. T.; Daasbjerg, K.; Skrydstrup, T. Nat. Commun. 2016, 7, 13782.
[48]	Jensen, M. T.; Rønne, M. H.; Ravn, A. K.; Juhl, R. W.; Nielsen, D. U.; Hu, X. M.; Pedersen, S. U.; Daasbjerg, K.; Skrydstrup, T. Nat. Commun. 2017, 8, 489.
[49]	Maji, S.; Das, A.; Bhatt, M. M.; Mandal, S. K. Nat. Catal. 2024, 7, 375.
[50]	Chen, X. W.; Yue, J. P.; Wang, K.; Gui, Y. Y.; Niu, Y. N.; Liu, J.; Ran, C. K.; Kong, W.; Zhou, W. J.; Yu, D. G. Angew. Chem., Int. Ed. 2021, 60, 14068.
[51]	Cerveri, A.; Giovanelli, R.; Sella, D.; Pedrazzani, R.; Monari, M.; Nieto Faza, O.; López, C. S.; Bandini, M. Chem.-Eur. J. 2021, 27, 7657. doi: 10.1002/chem.202101082 pmid: 33829576
[52]	Wang, M. M.; Lu, S. M.; Li, C. ACS Catal. 2022, 12, 10801.
[53]	Hu, Q.; Wei, B.; Wang, M.; Liu, M.; Chen, X. W.; Ran, C. K.; Wang, G.; Chen, Z.; Li, H.; Song, J.; Yu, D. G.; Guo, C. J. Am. Chem. Soc. 2024, 146, 14864.
[54]	Yue, J. P.; Xu, J. C.; Luo, H. T.; Chen, X. W.; Song, H. X.; Deng, Y.; Yuan, L.; Ye, J. H.; Yu, D. G. Nat. Catal. 2023, 6, 959.
[55]	Sun, G. Q.; Yu, P.; Zhang, W.; Zhang, W.; Wang, Y.; Liao, L. L.; Zhang, Z.; Li, L.; Lu, Z.; Yu, D. G.; Lin, S. Nature 2023, 615, 67.
[56]	Gui, Y. Y.; Chen, X. W.; Mo, X. Y.; Yue, J. P.; Yuan, R.; Liu, Y.; Liao, L. L.; Ye, J. H.; Yu, D. G. J. Am. Chem. Soc. 2024, 146, 2919.
[57]	Jiang, Y. X.; Liao, L. L.; Gao, T. Y.; Xu, W. H.; Zhang, W.; Song, L.; Sun, G. Q.; Ye, J. H.; Lan, Y.; Yu, D. G. Nat. Synth. 2024, 3, 394.
[58]	Sheta, A. M.; Fernández, S.; Liu, C.; Bandomo, G. C. D.; Fillol, J. L. Angew. Chem., Int. Ed. 2024, 63, e202403674.
[59]	Qiu, L. Q.; Li, H. R.; He, L. N. Acc. Chem. Res. 2023, 56, 2225.
[60]	Yang, Z. W.; Chen, J. M.; Qiu, L. Q.; Xie, W. J.; He, L. N. Angew. Chem., Int. Ed. 2022, 61, e202205301.
[61]	Zhao, L.; Xie, W. J.; Meng, Z. Z.; Li, H. R.; He, L. N. Org. Lett. 2024, 26, 3241. doi: 10.1021/acs.orglett.4c00860 pmid: 38578088
[62]	Kuang, S.; Xiao, T.; Chi, H.; Liu, J.; Mu, C.; Liu, H.; Wang, S.; Yu, Y.; Meyer, T. J.; Zhang, S.; Ma, X. Angew. Chem., Int. Ed. 2024, 63, e202316772.
[63]	Wang, M. Y.; Jin, X.; Wang, X.; Xia, S.; Wang, Y.; Huang, S.; Li, Y.; He, L. N.; Ma, X. Angew. Chem., Int. Ed. 2021, 60, 3984.
[64]	Fedorynski, M. Chem. Rev. 2003, 103, 1099.
[65]	Khodakov, A.Y.; Chu, W.; Fongarland, P. Chem. Rev. 2007, 107, 1692. doi: 10.1021/cr050972v pmid: 17488058
[66]	Halder, P.; Talukdar, V.; Iqubal, A.; Das, P. J. Org. Chem. 2022, 87, 13965.
[67]	Halder, P.; Iqubal, A.; Mondal, K.; Mukhopadhyay, N.; Das, P. J. Org. Chem. 2023, 88, 15218.
[68]	Zhao, H. Y.; Du, H. Y.; Yuan, X. R.; Wang, T. J.; Han, W. Green Chem. 2016, 18, 5782.
[69]	Nishida, Y.; Takeda, N.; Matsuno, K.; Miyata, O.; Ueda, M. Eur. J. Org. Chem. 2018, 2018, 3928.
[70]	Demselben Justus Liebigs Ann. Chem. 1862, 123, 121.
[71]	Panda, B.; Albano, G. Catalysts 2021, 11, 1531.
[72]	Mohanty, A.; Nayak, M. K.; Roy, S. Org. Biomol. Chem. 2023, 21, 5601.
[73]	Xu, F.; Li, D.; Han, W. Green Chem. 2019, 21, 2911.
[74]	Grushin, V. V.; Alper, H. Organometallics 1993, 12, 3846.
[75]	Makosza, M.; Wawrzyniewicz, W. Tetrahedron Lett. 1969, 10, 4669.
[76]	Clark, G. R.; Mareden, K.; Roper, W. R.; Wright, L. J. J. Am. Chem. Soc. 1980, 102, 1206.
[77]	Roper, W. R.; Wright, A. H. J. Organomet. Chem. 1982, 233, C69.
[78]	Clark, G. R.; Roper, W. R.; Wright, A. H. J. Organomet. Chem. 1982, 236, C7.
[79]	Roper, W. R. J. Organomet. Chem. 1986, 300, 167.
[80]	Gockel, S. N.; Hull, K. L. Org. Lett. 2015, 17, 3236.
[81]	Kannaboina, P.; Raina, G.; Kumarab, K. A.; Das, P. Chem. Commun. 2017, 53, 9446.
[82]	Liu, X.; Gu, Z. Org. Chem. Front. 2015, 2, 778.
[83]	Guo, S. R.; Santhosh Kumar, P.; Yuan, Y. Q.; Yang, M. H. Tetrahedron Lett. 2017, 58, 2681.
[84]	Sharma, P.; Rohilla, S.; Jain, N. J. Org. Chem. 2017, 82, 1105.
[85]	Nitha, P. R.; Joseph, M. M.; Gopalan, G.; Maiti, K. K.; Radhakrishnan, K. V.; Das, P. Org. Biomol. Chem. 2018, 16, 6430. doi: 10.1039/c8ob01486h pmid: 30132779
[86]	Wang, L.; Wang, H.; Li, G.; Min, S.; Xiang, F.; Zheng, W. Adv. Synth. Catal. 2018, 360, 4585.
[87]	Rathod, G. K.; Jain, R. J. Org. Chem. 2023, 88, 7219.
[88]	Markovič, M.; Lopatka, P.; Koóš, P.; Gracza, T. ChemistrySelect 2016, 1, 2454.
[89]	Kolomnikov, I. S.; Erman, M. P.; Kukolev, V. P.; Volpin, M. E. Kinet. Catal. 1972, 13, 227.
[90]	Simonato, J. P.; Walter, T.; Mtivier, P. J. Mol. Catal. A 2001, 171, 91.
[91]	Simonato, J. P. J. Mol. Catal. A 2003, 197, 61.
[92]	Fouad, M. A.; Ferretti, F.; Ragaini, F. J. Org. Chem. 2023, 88, 5108.
[93]	Fan, C.; Hou, J.; Chen, Y. J.; Ding, K. L.; Zhou, Q. L. Org. Lett. 2021, 23, 2074.
[94]	Hussain, N.; Chhalodia, A. K.; Ahmed, A.; Mukherjee, D. ChemistrySelect 2020, 5, 11272. doi: 10.1002/slct.202003395
[95]	Konishi, H.; Manabe, K. Tetrahedron Lett. 2019, 60, 151147.
[96]	Mondal, S.; Nandi, S.; Dasa, S.; Jana, R. Chem. Commun. 2024, 60, 13758.
[97]	Wang, L.; Neumann, H.; Beller, M. Angew. Chem., Int. Ed. 2018, 57, 6910.
[98]	Wu, F. P.; Peng, J. B.; Meng, L. S.; Qi, X. X.; Wu, X. F. ChemCatChem 2017, 9, 3121.
[99]	Friis, S. D.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. J. Am. Chem. Soc. 2011, 133, 18114. doi: 10.1021/ja208652n pmid: 22014278
[100]	Huang, H.; Yu, C.; Zhang, Y.; Zhang, Y.; Mariano, P. S.; Wang, W. J. Am. Chem. Soc. 2017, 139, 9799. doi: 10.1021/jacs.7b05082 pmid: 28692260
[101]	Huang, H.; Li, X.; Yu, C.; Zhang, Y.; Mariano, P. S.; Wang, W. Angew. Chem., Int. Ed. 2017, 56, 1500.
[102]	Shil, A. K.; Kumar, S.; Reddy, C. B.; Dadhwal, S.; Thakur, V.; Das, P. Org. Lett. 2015, 17, 5352.
[103]	Shao, C.; Lu, A.; Wang, X.; Zhou, B.; Guan, X.; Zhang, Y. Org. Biomol. Chem. 2017, 15, 5033.
[104]	Wang, Y.; Ren, W.; Li, J.; Wang, H.; Shi, Y. Org. Lett. 2014, 16, 5960.
[105]	Ren, W.; Sheng, X.; Fan, C.; Shi, Y. Org. Lett. 2023, 25, 7786.
[106]	Mehara, P.; Sharma, P.; Bains, R.; Sharma, A. K.; Das, P. Chem. Sci. 2024, 15, 18379.
[107]	Liu, X.; Portela, B. S.; Wiedenbeck, A.; Chrisman, C. H.; Paton, R. S.; Miyake, G. Angew. Chem., Int. Ed. 2024, 63, e202410928.
[108]	Du, S.; Wang, W. F.; Song, Y.; Chen, Z.; Wu, X. F. Org. Lett. 2021, 23, 974.
[109]	Wei, P.; Ying, J.; Wu, X. F. Org. Lett. 2023, 25, 7700.
[110]	Fu, L. Y.; Ying, J.; Wu, X. F. J. Org. Chem. 2019, 84, 12648.
[111]	Fu, L. Y.; Ying, J.; Qi, X. X.; Peng, J. B.; Wu, X. F. J. Org. Chem. 2019, 84, 1421.
[112]	Mu, B.; Xia, S.; Wu, L.; Li, J.; Li, Z.; Wang, Z.; Wu, J. J. Org. Chem. 2022, 87, 4918.
[113]	Lukasevics, L.; Cizikovs, A.; Grigorjeva, L. Org. Lett. 2020, 22, 2720. doi: 10.1021/acs.orglett.0c00672 pmid: 32181664
[114]	Yu, W. Y.; Sit, W. N.; Lai, K. M.; Zhou, Z.; Chan, A. S. C. J. Am. Chem. Soc. 2008, 130, 3304.
[115]	Wang, H.; Ying, J.; Lai, M.; Qi, X.; Peng, J. B.; Wu, X. F. Adv. Synth. Catal. 2018, 360, 1693.
[116]	Ying, J.; Wang, H.; Qi, X.; Peng, J. B.; Wu, X. F. Eur. J. Org. Chem. 2018, 5, 688.
[117]	Ying, J.; Zhou, C.; Wu, X. F. Org. Biomol. Chem. 2018, 16, 1065. doi: 10.1039/c7ob03145a pmid: 29363708
[118]	Zhu, Y.; Le, Z.; Ying, J.; Wu, X. F. J. Organomet. Chem. 2021, 956, 122115.
[119]	Wang, S.; Wang, J. S.; Ying, J.; Wu, X. F. Chin. Chem. Lett. 2023, 34, 107873.
[120]	Cacchi, S.; Fabrizi, G.; Goggiamani, A. Org. Lett. 2003, 5, 4269.
[121]	Ueda, T.; Konishi, H.; Manabe, K. Org. Lett. 2012, 14, 3100.
[122]	Fujihara, T.; Hosoki, T.; Katafuchi, Y.; Iwai, T.; Teraoa, J.; Tsuji, Y. Chem. Commun. 2012, 48, 8012.
[123]	Ueda, T.; Konishi, H.; Manabe, K. Tetrahedron Lett. 2012, 53, 5171.
[124]	Yan, X. B.; Wang, N.; Zhou, J.; Ge, H.; Wang, Z.; Lin, Y.; Shui, H. Org. Lett. 2024, 26, 6518.
[125]	Ueda, T.; Konishi, H.; Manabe, K. Org. Lett. 2012, 14, 5370.
[126]	Ye, H.; Wu, L.; Zhang, M.; Jiang, G.; Dai, H.; Wu, X. X. Chem. Commun. 2022, 58, 6825.
[127]	Barré, A.; Ţînţaş, M. L.; Alix, F.; Gembus, V.; Papamicaël, C.; Levacher, V. J. Org. Chem. 2015, 80, 6537.
[128]	Monrose, A.; Salembier, H.; Bousquet, T.; Pellegrini, S.; Pélinski, L. Adv. Synth. Catal. 2017, 359, 2699.
[129]	Wang, H.; Gao, Y.; Zhou, C.; Li, G. J. Am. Chem. Soc. 2020, 142, 8122. doi: 10.1021/jacs.0c03144 pmid: 32309942
[130]	Zhang, F.; Wu, X. Y.; Gao, P. P.; Zhang, H.; Li, Z.; Ai, S.; Li, G. Chem. Sci. 2024, 15, 6178.
[131]	Corey, E. J.; Hegedus, L. S. J. Am. Chem. Soc. 1969, 91, 1233.
[132]	Nakaya, R.; Yorimitsu, H.; Oshima, K. Chem. Lett. 2011, 40, 904.
[133]	Kaiser, N. F. K.; Hallberg, A.; Larhed, M. J. Comb. Chem. 2002, 4, 109.
[134]	Poral, V. L.; Furkert, D. P.; Brimble, M. A. Org. Lett. 2015, 17, 6214.
[135]	Wu, X. Y.; Ekegren, J. K.; Larhed, M. Organometallics 2006, 25, 1434.
[136]	Wu, X. Y.; Larhed, M. Org. Lett. 2005, 7, 3327.
[137]	Wu, X.Y.; Wannberg, J.; Larhed, M. Tetrahedron. 2006, 62, 4665.
[138]	Nordeman, P.; Odell, L. R.; Larhed, M. J. Org. Chem. 2012, 77, 11393. doi: 10.1021/jo302322w pmid: 23205569
[139]	He, L.; Sharif, M.; Neumann, H.; Beller, M.; Wu, X. F. Green Chem. 2014, 16, 3763.
[140]	Wannberg, J.; Larhed, M. J. Org. Chem. 2003, 68, 5750. pmid: 12839476
[141]	Qi, X. X.; Bao, Z. P.; Yao, X. T.; Wu, X. F. Org. Lett. 2020, 22, 6671.
[142]	Zhang, B.; Deng, W.; Xu, Z. Y. Organometallics 2023, 42, 588.
[143]	Preston, A.; Atkinson, S.; Bamborough, P.; Chung, C.; Craggs, P. D.; Gordon, L.; Grandi, P.; Gray, J. R. J.; Jones, E. J.; Lindon, M.; Michon, A. M.; Mitchell, D. J.; Prinjha, R. K.; Rianjongdee, F.; Rioja, I.; Seal, J.; Taylor, S.; Wall, I.; Watson, R. J.; Woolven, J.; Demont, E. H. J. Med. Chem. 2020, 63, 9070. doi: 10.1021/acs.jmedchem.0c00605 pmid: 32691591
[144]	Cheung, C. W.; Ploeger, M. L.; Hu, X. Chem. Sci. 2018, 9, 655. doi: 10.1039/c7sc03950f pmid: 29629132
[145]	Cheruku, S.; Sajith, A. M.; Narayana, Y.; Shetty, P.; Nagarakere, S. C.; Sagar, K. S.; Manikyanally, K. N.; Rangappa, K. S.; Mantelingu, K. J. Org. Chem. 2021, 86, 5530.
[146]	Dogga, B.; Kumar, C. S. A.; Joseph, J. T. Eur. J. Org. Chem. 2021, 2, 309.
[147]	Mou, Q.; Han, T.; Liu, M. Org. Lett. 2024, 26, 2169.
[148]	Huang, J.; Guo, W.; Wu, W.; Yin, F.; Wang, H.; Tao, C.; Zhou, H.; Hu, W. J. Org. Chem. 2024, 89, 2014.
[149]	Wang, M. Y.; Zeng, W. L.; Chen, L.; Yuan, Y. F.; Li, W. Angew. Chem., Int. Ed. 2024, 63, e202403917.
[150]	Gehrtz, P. H.; Hirschbeck, V.; Fleischer, I. Chem. Commun. 2015, 51, 12574.
[151]	Gøgsig, T. M.; Taaning, R. H.; Lindhardt, A. T.; Skrydstrup, T. Angew. Chem., Int. Ed. 2012, 51, 798.
[152]	Nielsen, D. U.; Taaning, R. H.; Lindhardt, A. T.; Gøgsig, T. M.; Skrydstrup, T. Org. Lett. 2011, 13, 4454.
[153]	Xin, Z.; Gøgsig, T. M.; Lindhardt, A. T.; Skrydstrup, T. Org. Lett. 2012, 14, 284.
[154]	Gøgsig, T. M.; Nielsen, D. U.; Lindhardt, A. T.; Skrydstrup, T. Org. Lett. 2012, 14, 2536.
[155]	Kochi, T.; Urano, S.; Seki, H.; Mizushima, E.; Sato, M.; Kakiuchi, F. J. Am. Chem. Soc. 2009, 131, 2792.
[156]	Kochi, T.; Tazawa, A.; Honda, K.; Kakiuchi, F. Chem. Lett. 2011, 40, 1018.
[157]	Markovič, M.; Lopatka, P.; Koóš, P.; Gracza, T. Org. Lett. 2015, 17, 5618. doi: 10.1021/acs.orglett.5b02840 pmid: 26555577
[158]	Hermange, P.; Lindhardt, A. T.; Taaning, R. H.; Bjerglund, K.; Lupp, D.; Skrydstrup, T. J. Am. Chem. Soc. 2011, 133, 6061.
[159]	Xu, S.; Wang, K.; Kong, W. Org. Lett. 2019, 21, 7498.
[160]	Boehm, P.; Roediger, S.; Bismuto, A.; Morandi, B. Angew. Chem., Int. Ed. 2020, 59, 17887.
[161]	Wang, J.; Yin, Y.; He, X.; Duan, Q. L.; Bai, R.; Shi, H. W.; Shi, R. ACS Catal. 2023, 13, 8161.
[162]	Huo, Y. W.; Bao, Z. P.; Wang, L. C.; Schmoll, A.; Wu, X. F. J. Catal. 2025, 442, 115890.
[163]	Gibson, S. E.; Stevenazzi, A. Angew. Chem., Int. Ed. 2003, 42, 1800.
[164]	Shibata, T. Adv. Synth. Catal. 2006, 348, 2328.
[165]	Ikeda, K.; Morimoto, T.; Kakiuchi, K. J. Org. Chem. 2010, 75, 6279.
[166]	Min, B. H.; Kim, D. S.; Park, H. S.; Jun, C. H. Chem.-Eur. J. 2016, 22, 6234.
[167]	Wang, Y.; Huang, W.; Wang, C.; Qu, J.; Chen, Y. Org. Lett. 2020, 22, 4245. doi: 10.1021/acs.orglett.0c01284 pmid: 32383891
[168]	Zhu, Y.; Chen, Z.; Liu, K.; Zhang, F.; Yuan, Q. Org. Biomol. Chem. 2017, 15, 8078.
[169]	Han, J.; Wang, N.; Huang, Z. B.; Zhao, Y.; Shi, D. Q. J. Org. Chem. 2017, 82, 6831.
[170]	Payne, C. M.; Cho, K.; Larsen, D. S. RSC Adv. 2019, 9, 30736.
[171]	Zoller, B.; Zapp, J.; Huy, P. H. Chem.-Eur. J. 2020, 26, 9632.
[172]	Zhu, W. Q.; Fang, Y. C.; Han, W. Y.; Li, F.; Yanga, M. G.; Chen, Y. Z. Org. Chem. Front. 2021, 8, 3082.
[173]	Li, Z. Z.; Li, W. D.; Fan, J.; Li, J. T.; Liu, Z. W.; Shi, X. Y. Org. Chem. Front. 2023, 10, 2243.
[174]	Li, X.; Shi, L.; Zhang, X.; Zhang, X. Org. Biomol. Chem. 2018, 16, 6438.
[175]	Wang, Z.; Yin, Z.; Wu, X. F. Chem. Commun. 2018, 54, 4798.
[176]	Wu, X.; Miao, J.; Li, Y.; Li, G.; Ge, H. Chem. Sci. 2016, 7, 5260.
[177]	Tien, C. H.; Trofimova, A.; Holownia, A.; Kwak, B. S.; Larson, R. T.; Yudin, A. K. Angew. Chem., Int. Ed. 2021, 60, 4342.
[178]	Holownia, A.; Tien, C. H.; Diaz, D. B.; Larson, R. T.; Yudin, A. K. Angew. Chem., Int. Ed. 2019, 58, 15148.
[179]	Wang, Y.; Tian, B.; Li, Y.; Li, W.; Chen, Z.; Liu, S.; Li, S. ChemSusChem 2024, 17, e202301324.
[180]	Espinoza-Hicks, C.; Montoya, P.; Bautista, R.; Jimenez-Vazquez, H. A.; Rodriguez-Valdez, L. M.; Camacho-Davila, A. A.; Cossio, F. P.; Delgado, F.; Tamariz, J. J. Org. Chem. 2018, 83, 5347. doi: 10.1021/acs.joc.7b02344 pmid: 29697257
[181]	Hou, Z.; Mao, J.; Yao, J.; Han, C.; Bi, R. Chem. Eng. J. 2024, 480, 148284.
[182]	Zhang, X.; Huang, L.; Zhang, Y.; Meng, F.; Dai, X.; Cheng, C.; Guo, Y.; Gao, Z. Org. Biomol. Chem. 2025, 23, 1190.
[183]	Liu, Y.; Zhang, Y.; Qu, Y.; Liu, Q.; Cao, K.; Yan, F.; Zhang, L.; Li, X.; Zhao, Z.; Liu, H. Green Chem. 2024, 27, 1348.
[184]	Huang, T.; Wu, X.; Yu, Y.; An, L.; Yin, X. Tetrahedron Lett. 2019, 60, 1667.
[185]	Kim, J. H.; Song, T.; Chung, Y. K. Org. Lett. 2017, 19, 1248.
[186]	McClure, J. D.; Slaugh, L. H. DE 2060863, 1971.
[187]	Behr, A.; Kanne, U.; Keim, W. J. Mol. Catal. 1986, 35, 19.
[188]	Jo, E. A.; Lee, J. H.; Jun, C. H. Chem. Commun. 2008, 44, 5779.
[189]	Moran, J.; Preetz, A.; Mesch, R. A.; Krische, M. J. Nat. Chem. 2011, 3, 287.
[190]	Serrano-Ruiz, J. C.; Luque, R.; Sepulveda-Escribano, A. Chem. Soc. Rev. 2011, 40, 5266. doi: 10.1039/c1cs15131b pmid: 21713268
[191]	Verendel, J. J.; Nordlund, M.; Andersson, P. G. ChemSusChem. 2013, 6, 426. doi: 10.1002/cssc.201200843 pmid: 23303703
[192]	Dai, X.; Adomeit, S.; Rabeah, J.; Kreyenschulte, C.; Brückner, A.; Wang, H. L.; Shi, F. Angew. Chem., Int. Ed. 2019, 58, 5251.
[193]	Nielsen, D. B.; Wahlqvist, B. A.; Nielsen, D. U.; Daasbjerg, K.; Skrydstrup, T. ACS Catal. 2017, 7, 6089.
[194]	Ikeda, K.; Morimoto, T.; Tsumagari, T.; Tanimoto, H.; Nishiyama, Y.; Kakiuchi, K. Synlett 2012, 23, 393.
[195]	Fuji, K.; Morimoto, T.; Tsutsumi, K.; Kakiuchi, K. Angew. Chem., Int. Ed. 2003, 42, 2409.
[196]	Park, K. H.; Jung, I. G.; Chung, Y. K. Org. Lett. 2004, 6, 1183.
[197]	Morimoto, T.; Fuji, K.; Tsutsumi, K.; Kakiuchi, K. J. Am. Chem. Soc. 2002, 124, 3806. pmid: 11942798
[198]	Shibata, T.; Toshida, N.; Takagi, K. Org. Lett. 2002, 4, 1619.
[199]	Liu, Q.; Yuan, K.; Arockiam, P. B.; Franke, R.; Doucet, H.; Jackstell, R.; Beller, M. Angew. Chem., Int. Ed. 2015, 54, 4493.
[200]	Natte, K.; Dumrath, A.; Neumann, H.; Beller, M. Angew. Chem., Int. Ed. 2014, 53, 10090.
[201]	Okano, T.; Kobayashi, T.; Konishi, H.; Kiji, J. Tetrahedron Lett. 1982, 23, 4967.
[202]	Ahn, H. S.; Han, S. H.; Uhm, S. J.; Seok, W. K.; Lee, H. N.; Korneeva, G. A. J. Mol. Catal. A 1999, 144, 295.
[203]	Gao, J.; He, X. C.; Liu, Y. L.; Yao, P. P.; Guan, J. P.; Chen, K.; Xiang, H. Y.; Yang, H. Org. Lett. 2024, 26, 1478.
[204]	Wu, X.; Zhao, Y.; Ge, H. J. Am. Chem. Soc. 2015, 137, 4924.
[205]	Chen, J.; Feng, J. B.; Natte, K.; Wu, X. F. Chem.-Eur. J. 2015, 21, 16370.
[206]	Chen, J.; Natte, K.; Wu, X. F. Tetrahedron Lett. 2015, 56, 6413.
[207]	Hosoi, K.; Nozaki, K.; Hiyama, T. Org. Lett. 2002, 4, 2849.
[208]	Tan, Y.; Lang, J.; Tang, M.; Li, J.; Mi, P.; Zheng, X. ChemistrySelect 2021, 6, 2343.
[209]	Kolekar, Y. A.; Saptal, V. B.; Bhanage, B. M. Chem.-Eur. J. 2023, 29, e202301381.
[210]	Ueda, T.; Konishi, H.; Manabe, K. Angew. Chem., Int. Ed. 2013, 52, 8611.
[211]	Ueda, T.; Konishi, H.; Manabe, K. Org. Lett. 2013, 15, 5370.
[212]	Nan, J.; Chen, P.; Gong, X.; Hu, Y.; Ma, Q.; Wang, B.; Ma, Y. Org. Lett. 2021, 23, 3761.
[213]	Cruz, L. K. D. L.; Bauer, N.; Cachuela, A.; Tam, W. S.; Tripathi, R.; Yang, X.; Wang, B. Org. Lett. 2022, 24, 4902.
[214]	Feng, C. C.; Zhang, S. L. Org. Biomol. Chem. 2023, 21, 728.
[215]	Sheng, H.; Chen, Z.; Song, Q. J. Am. Chem. Soc. 2024, 146, 1722.
[216]	Cao, M.; Zuo, D.; Wang, D.; Li, Y.; Zhao, J.; Tan, J.; Li, P. J. Org. Chem. 2024, 89, 5871.
[217]	Prasada, P. K.; Sudalai, A. Adv. Synth. Catal. 2014, 356, 2231.
[218]	Song, K. L.; Wu, B.; Gan, W. E.; Yang, W. C.; Chen, X. B.; Cao, J.; Xu, L. W. Org. Chem. Front. 2021, 8, 3398.
[219]	Zheng, Y.; Dong, M.; Qu, E.; Bai, J.; Wu, X. F.; Li, W. Chem.-Eur. J. 2021, 27, 16219.
[220]	Rao, K.; Sharma, A.; Rathod, G. K.; Barahdiaa, A. S.; Jain, R. Org. Biomol. Chem. 2025, 23, 980.
[221]	Sun, G. Q.; Liao, L. L.; Ran, C. K.; Ye, J. H.; Yu, D. G. Acc. Chem. Res. 2024, 57, 2728.
[222]	Song, L.; Wang, W.; Yue, J. P.; Jiang, Y. X.; Wei, M. K.; Zhang, H. P.; Yan, S. S.; Liao, L. L.; Yu, D. G. Nat. Catal. 2022, 5, 832.
[223]	Zhang, Z.; Ye, J. H.; Ju, T.; Liao, L. L.; Huang, H.; Gui, Y. Y.; Zhou, W. J.; Yu, D. G. ACS Catal. 2020, 10, 10871.
[224]	Chen, X. W.; Li, C.; Gui, Y. Y.; Yue, J. P.; Zhou, Q.; Liao, L. L.; Yang, J. W.; Ye, J. H.; Yu, D. G. Angew. Chem., Int. Ed. 2024, 63, e202403401.
[225]	Zhang, Z.; Liao, L. L.; Yan, S. S.; Wang, L.; He, Y. Q.; Ye, J. H.; Li, J.; Zhi, Y. G.; Yu, D. G. Angew. Chem., Int. Ed. 2016, 55, 7068.
[226]	Tortajada, A.; Hernández, F. J.; Börjesson, M.; Moragas, T.; Martin, R. Angew. Chem., Int. Ed. 2018, 57, 15948.
[227]	Yang, M.; Liu, L. B.; Liu, S.; Li, Y.; Ouyang, B.; Fu, X. Z.; Luo, J. L.; Sun, Y.; Liu, S. Chin. Chem. Lett. 2024, 35, 110603.
[228]	Li, P.; Wang, Y.; Zhao, H.; Qiu, Y. Acc. Chem. Res. 2025, 58, 113.
[229]	Lan, J.; Lu, X.; Ren, B.; Duo, F.; Niu, X.; Si, J. Org. Biomol. Chem. 2024, 22, 682.
[230]	Yuan, P.; Zhu, C.; Meng, Q. Chin. J. Org. Chem. 2024, 44, 2997 (in Chinese).
	(袁盼锋, 朱灿明, 孟庆元, 有机化学, 2024, 44, 2997.) doi: 10.6023/cjoc202405004
[231]	Xu, L.; Wu, A.; Yu, F.; Li, H.; He, L. Chin. J. Org. Chem. 2024, 44, 3091 (in Chinese).
	(许立锋, 武安国, 于芳羽, 李红茹, 何良年, 有机化学, 2024, 44, 3091.) doi: 10.6023/cjoc202406044
[232]	Gao, X.; Zhong, Y.; Feng, N.; Sun, Y.; Yang, D.; Zhou, F. Chin. J Org. Chem. 2024, 44, 3034 (in Chinese).
	(高小童, 钟昱卿, 冯楠, 孙莹, 杨得勇, 周锋, 有机化学, 2024, 44, 3034.)
[233]	Zhou, S.; Guan, Z.; Chen, G.; Wu, J.; Pan, Y.; Guo, Y.; Yang, Z. Fuel 2024, 377, 132539.
[234]	Shi, H.; Jia, S.; Dong, M.; Wu, H.; Huang, Z.; Dong, K. Org. Lett. 2024, 26, 8982.
[235]	Hu, Q. L.; Zhang, Z. X.; Zhang, J. J.; Li, S. M.; Wang, H.; Lu, J. X. ACS Omega 2020, 5, 3498.
[236]	Pitts, C. R.; Lectka, T. Chem. Rev. 2014, 114, 7930. doi: 10.1021/cr4005549 pmid: 24555548
[237]	Chi, D.; Qi, H.; Wang, L.; Chen, S. Chem. Commun. 2024, 60, 8613.
[238]	Majhi, J.; Molander, G. A. Angew. Chem., Int. Ed. 2024, 63, e202311853.
[239]	Xiao, W.; Zhang, J.; Wu, J. ACS Catal. 2023, 13, 15991.
[240]	Liu, W. W.; Xu, P.; Jiang, H. X.; Li, M. L.; Hao, T. Z.; Liu, Y. Q.; Zhu, S. L.; Zhang, K. X.; Zhu, X. ACS Catal. 2024, 14, 10053.
[241]	Xu, C. W.; Yan, S. Y.; Xu, H.; Wang, S.; Gu, L. Q.; Xu, P.; Yin, L.; Zhu, X. ACS Catal. 2024, 14, 11967.
[242]	Wu, Z.; Wu, M.; Zhu, K.; Wu, J.; Lu, Y. Chem 2023, 9, 978.