Catalytic functionalization of tertiary alcohols to fully substituted carbon centres

被引:141
作者
Chen, Long [1 ]
Yin, Xiao-Ping [1 ]
Wang, Cui-Hong [1 ]
Zhou, Jian [1 ]
机构
[1] E China Normal Univ, Dept Chem, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
关键词
ORGANOCATALYTIC ASYMMETRIC-SYNTHESIS; FRIEDEL-CRAFTS ALKYLATION; 3,3-DISUBSTITUTED OXINDOLES; NUCLEOPHILIC-SUBSTITUTION; ENANTIOSELECTIVE CONSTRUCTION; 3-SUBSTITUTED OXINDOLES; SPIROCYCLIC OXINDOLES; ALPHA-HYDROXYKETONES; FACILE PREPARATION; RITTER REACTION;
D O I
10.1039/c4ob00718b
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The catalytic nucleophilic substitution of tertiary alcohols using carbon. or heteroatom based nucleophiles is a versatile methodology for the efficient, diverse and atom economical construction of fully substituted carbon centres, including both quaternary carbons and heteroatom substituted tetrasubstituted carbons, which only produces water as the by-product. This review summarizes the recent progress in this field, including the catalytic asymmetric studies and their application in the natural product synthesis, briefly discusses the reaction mechanism and challenges, and outlines synthetic opportunities that are still open.
引用
收藏
页码:6033 / 6048
页数:16
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