Heck macrocyclization in natural product total synthesis

被引:18
作者
Zhang, Weicheng [1 ]
机构
[1] Nankai Univ, Tianjin Key Lab Mol Drug Res, Coll Pharm, State Key Lab Med Chem Biol, Tianjin 300353, Peoples R China
基金
中国国家自然科学基金;
关键词
PALLADIUM-CATALYZED CYCLIZATION; STEREOSELECTIVE TOTAL-SYNTHESIS; RNA-POLYMERASE INHIBITOR; RING-CLOSING METATHESIS; ACTIN-BINDING MACROLIDE; FORMAL TOTAL-SYNTHESIS; 2ND TOTAL-SYNTHESIS; ALPHA-BETA-TUBULIN; BIOLOGICAL EVALUATION; DIAZONAMIDE-A;
D O I
10.1039/d0np00087f
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Covering: 1981-2020 Heck macrocyclization is a logical extension of the award-winning Mizoroki-Heck reaction. Through covalent linking of two otherwise discrete coupling partners, the resultant chimeric substrate is transformed into a large ring with enhanced rigidity and unique functional group disposition. Pioneered in the early 1980s, this methodology has evolved into a competent option for creating diverse macrocycles. Despite its growing influence, hitherto no systematic survey has ever appeared in the literature. The present review delineates the state-of-the-art of Heck macrocyclization in the context of natural product synthesis. Sixteen selected cases, each examined from a different perspective, coalesce into the view that the title reaction is a viable tool for synthesis-enabled macrocycle research.
引用
收藏
页码:1109 / 1135
页数:27
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