[1] (a) Mascaretti, O. A.; Danelon, G. O.; Laborde, M.; Mata, E. G.; Setti, E. L. Curr. Pharm. Des. 1999, 5, 939. (b) Singh, G. S. Mini-Rev. Med. Chem. 2004, 4, 69. (c) Marson, C. M. Chem. Soc. Rev. 2011, 40, 5514. (d) Beniddir, M. A.; Evanno, L.; Joseph, D.; Skiredj, A.; Poupon, E. Nat. Prod. Rep. 2016, 33, 820. (e) Fan, Y.-Y.; Gao, C.-H.; Yue, J.-M. Sci. China Chem. 2016, 59, 1126. (f) Talele, T. T. J. Med. Chem. 2016, 59, 8712. (g) Croft, R. A.; Davis, O. A.; Doran, R.; Morgan, K. F. Chem. Rev. 2016, 116, 12150. (h) Decuyper, L.; Jukic, M.; Sosic, I.; Zula, A.; D’Hooghe, M.; Gobec, S. Med. Res. Rev. 2018, 38, 426. (i) Bauer, M. R.; Di Fruscia, P.; Lucas, S. C. C.; Michelides, I. N.; Nelson, J. E.; Sorer, R. I.; Whitehurst, B. C. RSC Med. Chem. 2021, 12, 448. (j) Hancock, E. N.; Brown, M. K. Chem. Eur. J. 2021, 27, 565. (k) Hui, C.; Liu, Y.; Jiang, M.; Wu, P. Trends Chem. 2022, 4, 677. (l) van der Kolk, M. R.; Janssen, M. A. C. H.; Rutjes, F. P. J. T.; Blanco-Ania, D. ChemMedChem 2022, 17, e202200020. (m) Kelly, C.B.; Milligan, J. A.; Tilley, L. J.; Sodano, T. M. Chem. Sci. 2022, 13, 11721. (n) Yang, P.; Jia, Q.; Song, S.; Huang, X. Nat. Prod. Rep. 2023, 40, 1094. [2] (a) Dolbier, Jr., W. R. Acc. Chem. Res. 1981, 14, 195. (b) Page, M. I. The Chemistry of β-Lactams, Blackie, 1993. (c) Dolbier, Jr., W. R.; Battiste, M. A. Chem. Rev. 2003, 103, 1071. (d) Fedoryński, M. Chem. Rev. 2003, 103, 1099. (e) Lee-Ruff, E.; Mladenova, G. Chem. Rev. 2003, 103, 1449. (f) Namyslo, J. C.; Kaufmann, D. E. Chem. Rev. 2003, 103, 1485. (g) Alcaide, B.; Almendros, P.; Aragoncillo, C. Chem. Rev. 2007, 107, 4437. (h) Seiser, T.; Saget, T.; Tran, D. N.; Cramer, N. Angew. Chem. Int. Ed. 2011, 50, 7740. (i) Banik, B. K. β-Lactams: Unique Structures of Distinctionfor Novel Molecules, Topics in Heterocyclic Chemistry; Springer GmbH, 2013, vol. 30. (j) Matsuda, T. Cleavage of Carbon-Carbon Single Bonds by Transition Metals; Chapter 3, Eds.: Murakami, M.; Chatani, N.; Wiley-VCH, Weinheim, 2016, pp 89. (k) Song, X.; Xu, C.; Wang, M. Tetrahedron Lett. 2017, 58, 1806. (l) Ombito, J. O.; Singh, G. S. Mini-Rev. Org. Chem. 2019, 16, 544. (m) Cohen, Y.; Cohen, A.; Marek, I. Chem. Rev. 2021, 121, 140. (n) Murakami, M.; Ishida, N. Chem. Rev. 2021, 121, 264. (o) Nanda, T.; Fastheem, M.; Linda, A.; Pati, B. V.; Banjare, S. K.; Biswal, P.; Ravikumar, P. C. ACS Catal. 2022, 12, 13247. [3] (a) Secci, F.; Frongia, A.; Piras, P. P. Molecules 2013, 18, 15541. (b) Pitts, C. R.; James, T. L.; Bull, A. Chem. Rev. 2014, 114, 7930. (c) Carreira, E. M.; Fessard, T. C. Chem. Rev. 2014, 114, 8257. (d) Xu, Y.; Conner, M. L.; Brown, M. K. Angew. Chem. Int. Ed. 2015, 54, 11918. (e) Poplata, S.; Tröster, A.; Zou, Y.-Q.; Bach, T. Chem. Rev. 2016, 116, 9748. (f) Wang, M.; Lu, P. Org. Chem. Front. 2018, 5, 254. (g) Li, J.; Gao, K.; Bian, M.; Ding, H. Org. Chem. Front. 2020, 7, 136. (h) Wen, K.-G.; Peng, Y.-Y.; Zeng, X.-P. Org. Chem. Front. 2020, 7, 2576. (i) Volochnyuk, D. M.; Grygorenko, O. O. Synthesis of gem-Diffuorocyclopropanes. In Emerging Fluorinated Motifs: Synthesis, Properties, and Applications; Ma, J.-A.; Cahard, D., Eds.; Wiley-VCH, 2020, pp 135-194. (j) Adekenova, K. S.; Wyatt, P. B.; Adekenov, S. M. Beilstein J. Org. Chem. 2021, 17, 245. (k) Wang, M.; Zhong, C.; Lu, P. Synlett 2021, 32, 1253. (l) Genzink, M. J.; Kidd, J. B.; Swords, W. B.; Yoon, T. P. Chem. Rev. 2022, 122, 1654. (m) Großkopf, J.; Kratz, T.; Rigotti, T.; Bach, T. Chem. Rev. 2022, 122, 1626. (n) Chen, J.; Zhou, Q.; Fang, H.; Lu, P. Chin. J. Chem. 2022, 40, 1346. (o) Hui, C.; Craggsc, L.; Antonchick, A. P. Chem. Soc. Rev. 2022, 51, 8652. (p) Hui, C.; Wang, Z.; Xie, Y.; Liu, J. Green Synth. Catal. 2023, 4, 1. (q) Yang, P.; Jia, Q.; Song, S.; Huang, X. Nat. Prod. Rep. 2023, 40, 1094. (r) Franceschi, P.; Cuadros, S.; Goti, G.; Dell’Amico, L. Angew. Chem. Int. Ed. 2023, 62, No. e202217210. [4] (a) Noyori, R.; Tokunaga, M.; Kitamura, M. Bull. Chem. Soc. Jpn. 1995, 68, 36. (b) Tang, W.; Zhang, X. Chem. Rev. 2003, 103, 3029. (c) Gladiali, S.; Alberico, E. Chem. Soc. Rev. 2006, 35, 226. (d) Ikariya, T.; Blacker, A. J. Acc. Chem. Res. 2007, 40, 1300. (e) Minnaard, A. J.; Feringa, B. L.; Lefort, L.; de Vries, J. G. Acc. Chem. Res. 2007, 40, 1267. (f) Shultz, C. S.; Krska, S. W. Acc. Chem. Res. 2007, 40, 1320. (g) Shimizu, H.; Nagasaki, I.; Matsumura, K.; Sayo, N.; Saito, T. Acc. Chem. Res. 2007, 40, 1385. (h) Gridnev, I. D.; Imamoto, T. Chem. Commun. 2009, 7447. (i) Xie, J.-H.; Zhu, S.-F.; Zhou, Q.-L. Chem. Rev. 2011, 111, 1713. (j) Wang, D.-S.; Chen, Q.-A.; Lu, S.-M.; Zhou, Y.-G. Chem. Rev. 2012, 112, 2557. (k) Bartoszewicz, A.; Ahlsten, N.; Martín-Matute, B. Chem. Eur. J. 2013, 19, 7274. (l) Verendel, J. J.; Pàmies, O.; Diéguez, M.; Andersson, P. G. Chem. Rev. 2014, 114, 2130. (m) Wang, Y.; Zhang, Z.; Zhang, W. Chin. J. Org. Chem. 2015, 35, 528. (n) Zhao, D.; Candish, L.; Paul, D.; Glorius, F. ACS Catal. 2016, 6, 5978. (o) Zhang, Z.; Butt, N. A.; Zhang, W. Chem. Rev. 2016, 116, 14769. (p) Wang, Z.; Zhang, Z.; Liu, Y.; Zhang, W. Chin. J. Org. Chem. 2016, 36, 447. (q) Yuan, Q.; Zhang, W. Chin. J. Org. Chem. 2016, 36, 274. (r) Wang, Q.; Zhao, S.; Jin, L.; Chen, X. Chin. J. Org. Chem. 2016, 36, 2242. (s) Yu, Y.-N.; Xu, M.-H. Acta Chim. Sinica 2017, 75, 655. (t) Foubelo, F.; Nájera, C.; Yus, M. Tetrahedron Asymmetry 2015, 26, 769. (u) Wang, D.; Astruc, D. Chem. Rev. 2015, 115, 6621. (v) Echeverria, P.-G.; Ayad, T.; Phansavath, P.; Ratovelomanana-Vidal, V. Synthesis 2016, 48, 2523. (w) Ayad, T.; Phansavath, P.; Ratovelomanana-Vidal, V. Chem. Rec. 2016, 16, 2754. (x) Bartlett, S. L.; Johnson, J. S. Acc. Chem. Res. 2017, 50, 2284-2296. (y) Seo, C. S. G.; Morris, R. H. Organometallics 2019, 38, 47. (z) Talavera, G.; Fariña, A. S.; Zanotti-Gerosa, A.; Nedden, H. G. Top. Organomet. Chem. 2019, 65, 73. (aa) Betancourta, R. M.; Echeverriab, P.-G.; Ayada, T.; Phansavath, P.; Ratovelomanana-Vidal, V. Synthesis 2021, 53, 30. (ab) Cotman, A. E. Chem. Eur. J. 2021, 27, 39. (ac) Ratovelomanana-Vidal, V.; Phansavath P. Asymmetric Hydrogenation and Transfer Hydrogenation; Wiley, Hoboken, NJ, 2021. (ad) Genêt, J.-P.; Phansavath, P.; Ratovelomanana-Vidal, V. Isr. J. Chem. 2021, 61, 409. (ae) Echeverria, P.-G.; Zheng, L.-S.; Llopis, Q.; He, B.; Westermeyer, A.; Betancourt, R. M.; Phansavath, P.; Ratovelomanana-Vidal, V. SynOpen 2022, 6, 75. (af) Caleffi, G. S.; Demidoff, F. C.; Nájera, C.; Costa, P. R. R. Org. Chem. Front. 2022, 9, 1165. (ag) Yang, S.; Fang, X. Tetrahedron 2023, 145, 133609. (ah) Bacheley, L.; Guillamot, G.; Phansavath, P.; Ratovelomanana-Vidal, V. Tetrahedron 2024, 152, 133781. [5] Xia, J.; Nie, Y.; Yang, G.; Liu, Y.; Gridnev, I. D.; Zhang, W. Chin. J. Chem. 2018, 36, 612. [6] Wang F.; Tan X.; Wu T.; Zheng L.-S.; Chen G.-Q.; Zhang X. Chem. Commun.2020, 56, 15557. [7] Lan S.; Huang H.; Liu W.; Xu C.; Lei X.; Dong W.; Liu J.; Yang S.; Cotman A.E.; Zhang Q.; Fang, X. J. Am. Chem. Soc.2024, 146, 4942 [8] Lan S.; Luo Y.; Jiang C.; Xu C.; Zhao L.; Lei X.; Dong J.; Liu J.; Yang S.; Zhang Q.; Fang, X. Angew. Chem. Int. Ed.2025, 64,e202512543. [9] Charron O.; Kosiuha M.; Ratovelomanana-Vidal V.; Phansavath P.; Gontard G.; Meyer, C. Adv. Synth. Catal.2025, 367, e202401406. [10] Charron O.; Kosiuha M.; Phansavath P.; Ratovelomanana-Vidal V.; Meyer C. Org. Lett.2026, 28, 1368-1373. [11] Yamani K.; Pierre H.; Archambeau A.; Meyer C.; Cossy, J. Angew. Chem. Int. Ed.2020, 59, 18505. [12] Charron O.; Kosiuha M.; Phansavath P.; Ratovelomanana-Vidal V.; Gontard G.; Meyer, C. J. Org. Chem.2024, 89, 14073. [13] Yin S.-N.; Liu Z.; Zhang X.; Zhou Y.-G.; Chen, M.-W. Adv. Synth. Catal.2025, 367, e70169. |