Chiral Bronsted acids in enantioselective carbonyl activations - activation modes and applications

被引:473
作者
Rueping, Magnus [1 ]
Kuenkel, Alexander [1 ]
Atodiresei, Iuliana [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Organ Chem, D-52074 Aachen, Germany
关键词
HETERO-DIELS-ALDER; FRIEDEL-CRAFTS ALKYLATION; BAEYER-VILLIGER REACTION; PHOSPHORIC-ACID; MUKAIYAMA-ALDOL; 3-SUBSTITUTED CYCLOBUTANONES; NAZAROV CYCLIZATION; MICHAEL ADDITION; ALDEHYDES; CATALYST;
D O I
10.1039/c1cs15087a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral phosphoric acids and derivatives have attracted considerable attention as a powerful tool in asymmetric catalysis. Various enantioselective reactions have been developed by using these efficient Bronsted acid organocatalysts. Although initially the activation was restricted to reactive Bronsted basic substrates, recent reports are demonstrating the versatility of phosphoric acid catalysts in the activation of carbonyl compounds in a stereochemically controlled fashion. This tutorial review gives an overview of enantioselective Bronsted acid catalyzed transformations with the main focus on carbonyl activation. Different activation modes, key features of the catalysts and the applied substrates are presented and discussed with the goal to elucidate the origin of stereoselectivity in these Bronsted acid catalyzed transformations.
引用
收藏
页码:4539 / 4549
页数:11
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