Catalytic asymmetric synthesis of tetrahydrocarbazoles

被引:42
作者
Tan, Fen [1 ]
Cheng, Hong-Gang [2 ]
机构
[1] Hubei Univ Educ, Hubei Key Lab Purificat & Applicat Plant Anticanc, 129 Gaoxin 2nd Rd, Wuhan 430205, Hubei, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
DIELS-ALDER REACTIONS; FRIEDEL-CRAFTS ALKYLATIONS; EFFICIENT ROUTE; FUNCTIONALIZED TETRAHYDROCARBAZOLES; ENANTIOSELECTIVE SYNTHESIS; DECARBOXYLATIVE ALLYLATION; O-QUINODIMETHANES; FORMAL SYNTHESIS; ALPHA-ARYLATION; COMPLEX;
D O I
10.1039/c9cc02486g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral tetrahydrocarbazoles (THCs) are prevalent in numerous natural indole alkaloids as well as synthetic pharmaceuticals, and exhibit a broad spectrum of bioactivities. As such, the development of efficient synthetic methodologies for the synthesis of chiral THCs is of substantial interest. The advent of asymmetric catalysis provides a powerful platform to assemble chiral THC motifs and great efforts have been devoted to this field over the past decades. In this feature article, we summarise recent advances in catalytic asymmetric synthesis of THCs, with particular emphases on reaction types and reaction mechanism.
引用
收藏
页码:6151 / 6164
页数:14
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