中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Total Synthesis of the Cephalotaxus Alkaloid (-)-Cephalotine A

文献类型:期刊论文

作者Sheng,Peng-Zhen; Li,Lu-Lu; Ni,Zhi-Bin; Wei,Kun; Yang,Yu-Rong
刊名ORGANIC LETTERS
出版日期2023
关键词FORMAL TOTAL-SYNTHESIS ALPHA-ALLYLATION UNIFIED STRATEGY NATURAL-PRODUCTS GAMMA-LACTAMS HECK REACTION (+/-)-CEPHALOTAXINE REARRANGEMENT C
ISSN号1523-7052
DOI10.1021/acs.orglett.3c02097
英文摘要Cephalotine A, a recently isolated Cephalotaxus alkaloid,was firstsynthesized enantioselectively through three critical reactions. SmI2 -mediated radical cyclization of lactone and aldehyde toforge the final ring system, Chang's iridium-catalyzed C-Hamidation to construct pyrrolidone stereoselectively, and Carreria'sdual Ir/amine catalyzed allylation to install the vicinal tertiarystereocenters.
WOS记录号WOS:001047853100001
源URL[http://ir.kib.ac.cn/handle/151853/75283]  
专题中国科学院昆明植物研究所
推荐引用方式
GB/T 7714
Sheng,Peng-Zhen,Li,Lu-Lu,Ni,Zhi-Bin,et al. Enantioselective Total Synthesis of the Cephalotaxus Alkaloid (-)-Cephalotine A[J]. ORGANIC LETTERS,2023.
APA Sheng,Peng-Zhen,Li,Lu-Lu,Ni,Zhi-Bin,Wei,Kun,&Yang,Yu-Rong.(2023).Enantioselective Total Synthesis of the Cephalotaxus Alkaloid (-)-Cephalotine A.ORGANIC LETTERS.
MLA Sheng,Peng-Zhen,et al."Enantioselective Total Synthesis of the Cephalotaxus Alkaloid (-)-Cephalotine A".ORGANIC LETTERS (2023).

入库方式: OAI收割

来源:昆明植物研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。