Catalytic diastereoselective construction of multiple contiguous quaternary carbon stereocenters via [2+2] cycloaddition and mechanistic insight

被引:10
作者
Wang, Xi [1 ,2 ]
Liu, Fujie [1 ,2 ]
Xu, Tao [1 ,2 ,3 ]
机构
[1] Ocean Univ China, Mol Synth Ctr, Sch Med & Pharm, Minist Educ, Qingdao 266003, Peoples R China
[2] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Minist Educ, Qingdao 266003, Peoples R China
[3] Pilot Natl Lab Marine Sci & Technol, Lab Marine Drugs & Bioprod, Qingdao 266237, Peoples R China
基金
中国国家自然科学基金;
关键词
Contiguous quaternary carbon stereocenters; 2+2] Cycloaddition; Fused ring system; STEREODIVERGENT SYNTHESIS; SYNTHETIC STRATEGIES; NATURAL-PRODUCTS; PHOTOCYCLOADDITION; DITERPENE; TAXANE;
D O I
10.1016/j.cclet.2022.06.047
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multiple contiguous quaternary carbon stereocenters (CQS) are highly challenging, yet important struc-tural motifs in organic synthesis. Here, we describe a visible light induced catalytic [2 + 2] cycloaddition approach that constructed up to four CQS in a pentacyclic fused ring system diastereoselectively, from the readily accessible dienamides with pendent heteroaryls. Variously substituted dienamides have been cyclized with heteroaryls to provide a range of novel CQS-containing scaffolds (26 examples, up to 96% yield and > 20:1 dr ratio). Mechanistic studies revealed that it may proceed through an uncommon beta-C radical initiated 7-endo cyclization from the biradical intermediate.(c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
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页数:5
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