Chinese Journal of Organic Chemistry ›› 2025, Vol. 45 ›› Issue (12): 4433-4442.DOI: 10.6023/cjoc202503021 Previous Articles Next Articles
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收稿日期:2025-04-17
修回日期:2025-05-04
发布日期:2025-06-19
通讯作者:
苏贤斌
Rong Cheng, Yiyi Qian, Yuanqiang Xu, Xianbin Su*(
)
Received:2025-04-17
Revised:2025-05-04
Published:2025-06-19
Contact:
Xianbin Su
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Rong Cheng, Yiyi Qian, Yuanqiang Xu, Xianbin Su. Liquid-Phase Synthesis of Peptide Alcohol Assisted by a Hydrophobic Silica-Based Tag[J]. Chinese Journal of Organic Chemistry, 2025, 45(12): 4433-4442.
| Reagent | DBF/Fulvene adducta | Washing solvent | Removal rateb/% | Yieldc/% |
|---|---|---|---|---|
| Piperidine | 6∶94 | HCl aq | 100 | 89 |
| Pyrrolidine | 16∶84 | HCl aq | 100 | 76 |
| DBU/Mps | >99 | K2CO3 aq | 100 | 98 |
| Reagent | DBF/Fulvene adducta | Washing solvent | Removal rateb/% | Yieldc/% |
|---|---|---|---|---|
| Piperidine | 6∶94 | HCl aq | 100 | 89 |
| Pyrrolidine | 16∶84 | HCl aq | 100 | 76 |
| DBU/Mps | >99 | K2CO3 aq | 100 | 98 |
| Reagent (mmol) | DBU/mmol | DMSO/EA (volume ratio) | DBF/Fulvene adducta | Washing solvent | Removal rateb/% | Yieldc/% |
|---|---|---|---|---|---|---|
| Mps (5) | 3 | 1∶1 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 1∶1 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 3∶7 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 2∶8 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (2) | 1 | 2∶8 | >99 | K2CO3 (aq.) | 100 | 98 |
| Reagent (mmol) | DBU/mmol | DMSO/EA (volume ratio) | DBF/Fulvene adducta | Washing solvent | Removal rateb/% | Yieldc/% |
|---|---|---|---|---|---|---|
| Mps (5) | 3 | 1∶1 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 1∶1 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 3∶7 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (5) | 1 | 2∶8 | >99 | K2CO3 (aq.) | 100 | 98 |
| Mps (2) | 1 | 2∶8 | >99 | K2CO3 (aq.) | 100 | 98 |
| Entry | Coupling reagent (mmol) | Conversiona/% | Yieldb/% |
|---|---|---|---|
| 1 | HATU (1.5) | 100 | 93 |
| 2 | DIC (1.5) | 100 | 90 |
| 3 | EDC•HCl (1.5) | 100 | 98 |
| 4 | EDC•HCl (1.1) | 100 | 98 |
| 5 | EDC•HCl (1.0) | 96 | 92 |
| Entry | Coupling reagent (mmol) | Conversiona/% | Yieldb/% |
|---|---|---|---|
| 1 | HATU (1.5) | 100 | 93 |
| 2 | DIC (1.5) | 100 | 90 |
| 3 | EDC•HCl (1.5) | 100 | 98 |
| 4 | EDC•HCl (1.1) | 100 | 98 |
| 5 | EDC•HCl (1.0) | 96 | 92 |
| SPPS | Tag-assisted LPPS | |||
|---|---|---|---|---|
| Material | Dosage/kg | Material | Dosage/kg | |
| CTC Resin (1 mmol/g) | 1.00 | CBTBS | 0.46 | |
| Fmoc-AA-OH | 8.32 | Fmoc-AA-OH | 2.74 | |
| Coupling reagent | 5.47 | Coupling reagent | 1.09 | |
| DMF | 64.23 | EA | 2.71 | |
| Piperidine | 5.89 | DBU/Mps | 3.08 | |
| SPPS | Tag-assisted LPPS | |||
|---|---|---|---|---|
| Material | Dosage/kg | Material | Dosage/kg | |
| CTC Resin (1 mmol/g) | 1.00 | CBTBS | 0.46 | |
| Fmoc-AA-OH | 8.32 | Fmoc-AA-OH | 2.74 | |
| Coupling reagent | 5.47 | Coupling reagent | 1.09 | |
| DMF | 64.23 | EA | 2.71 | |
| Piperidine | 5.89 | DBU/Mps | 3.08 | |
| [1] |
(a)
doi: 10.1038/s41573-019-0053-0 |
|
(b)
doi: 10.1038/nrd3148 |
|
|
(c)
doi: 10.6023/cjoc202403015 |
|
|
(彭伟, 程蓉, 刘豪, 刘冬梅, 苏贤斌, 有机化学, 2024, 44, 2876.)
doi: 10.6023/cjoc202403015 |
|
|
(d)
|
|
|
(刘豪, 刘冬梅, 孙浩田, 夏超, 苏贤斌, 高等学校化学学报, 2024, 45, 9.)
|
|
|
(e)
doi: 10.6023/A23100448 |
|
|
(王博, 蔡向东, 肖建喜, 化学学报, 2024, 82, 367.)
doi: 10.6023/A23100448 |
|
|
(f)
doi: 10.6023/A21120580 |
|
|
(尹昊, 陈西同, 付邢言, 马艳楠, 徐以梅, 张特, 梁帅, 杜姗姗, 齐昀坤, 王克威, 化学学报, 2022, 80, 444.)
doi: 10.6023/A21120580 |
|
| [2] |
|
| [3] |
doi: 10.1021/acs.joc.9b02348 pmid: 31755712 |
| [4] |
(a)
doi: 10.1002/anie.200904276 pmid: 2479100 |
|
(b)
pmid: 2479100 |
|
| [5] |
pmid: 2447070 |
| [6] |
|
| [7] |
|
|
姬中伟, 博士论文, 江南大学, 无锡, 2020).
|
|
| [8] |
doi: S0308-8146(17)31726-0 pmid: 29287362 |
| [9] |
doi: 10.1016/j.arr.2016.08.001 pmid: 27521253 |
| [10] |
pmid: 16998827 |
| [11] |
doi: 10.1002/chem.201903965 pmid: 31609031 |
| [12] |
doi: 10.1016/j.msec.2017.03.125 |
| [13] |
doi: 10.1002/cplu.201900749 pmid: 32237227 |
| [14] |
(a)
doi: 10.1039/C1OB06178J |
|
(b)
doi: 10.1002/psc.v15:9 |
|
| [15] |
doi: 10.1021/acsmedchemlett.0c00456 pmid: 33214850 |
| [16] |
doi: 10.1039/D0OB01417F |
| [17] |
doi: 10.1039/C6CC04245G |
| [18] |
pmid: 7966134 |
| [19] |
doi: 10.1042/bj0610264 |
| [20] |
doi: 10.1002/adsc.v366.11 |
| [21] |
doi: 10.1039/C7GC00247E |
| [22] |
doi: 10.1039/C9GC03982A |
| [23] |
doi: 10.1039/D0RA07204D |
| [24] |
doi: 10.1021/acs.organomet.1c00343 |
| [25] |
doi: 10.1002/anie.201702931 pmid: 28504858 |
| [26] |
(a)
doi: 10.1039/D1GC00603G |
|
(b)
doi: 10.1039/D1GC00604E |
|
|
(c)
doi: 10.1021/acs.oprd.7b00389 |
|
|
(d)
doi: 10.1002/cssc.v13.19 |
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