中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Total Syntheses of Cinchona Alkaloids via Photoredox-Catalyzed Deoxygenative Arylation

文献类型:期刊论文

作者Li,Lei; Yang,Hua-Fei; Ding,Qian-Hui; Wei,Kun; Yang,Yu-Rong
刊名ORGANIC LETTERS
出版日期2023
关键词ASYMMETRIC TOTAL SYNTHESES ALPHA-ALLYLATION FORMAL SYNTHESIS QUININE
ISSN号1523-7052
DOI10.1021/acs.orglett.3c01659
英文摘要Metallaphotoredox-enableddeoxygenative arylation of alcohols isa recently developed robust synthetic strategy for sp(2)-sp(3) coupling by MacMillan. Inspired by this method, we reportherein its first utilization in natural product total synthesis throughrealizing the coupling of 4-bromo-quinoline or 4-bromo-6-methoxyquinolinewith quincorine or quincoridine, respectively. The alcohols were denovo synthesized in racemic form by a key step of the intramolecularDiels-Alder reaction or in an enantioselective manner by Ir/aminedual-catalyzed allylation. All members of the cinchona alkaloids couldbe prepared efficiently.
学科主题Chemistry
WOS记录号WOS:001006586100001
源URL[http://ir.kib.ac.cn/handle/151853/75284]  
专题中国科学院昆明植物研究所
推荐引用方式
GB/T 7714
Li,Lei,Yang,Hua-Fei,Ding,Qian-Hui,et al. Total Syntheses of Cinchona Alkaloids via Photoredox-Catalyzed Deoxygenative Arylation[J]. ORGANIC LETTERS,2023.
APA Li,Lei,Yang,Hua-Fei,Ding,Qian-Hui,Wei,Kun,&Yang,Yu-Rong.(2023).Total Syntheses of Cinchona Alkaloids via Photoredox-Catalyzed Deoxygenative Arylation.ORGANIC LETTERS.
MLA Li,Lei,et al."Total Syntheses of Cinchona Alkaloids via Photoredox-Catalyzed Deoxygenative Arylation".ORGANIC LETTERS (2023).

入库方式: OAI收割

来源:昆明植物研究所

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