Bimetallic Rhodium(II)/Indium(III) Relay Catalysis for Tandem Insertion/Asymmetric Claisen Rearrangement

被引:57
作者
Chen, Yushuang [1 ]
Dong, Shunxi [1 ]
Xu, Xi [1 ]
Liu, Xiaohua [1 ]
Feng, Xiaoming [1 ]
机构
[1] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
1,2,3-triazoles; asymmetric catalysis; rearrangement; relay catalysis; tandem reaction; AMINO ACID-DERIVATIVES; DOYLE-KIRMSE REACTION; CHIRAL BETA-AMINO; ONE-POT SYNTHESIS; C-H ACTIVATION; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; TERMINAL ALKYNES; DONOR/ACCEPTOR CARBENOIDS; INDIUM CATALYSTS;
D O I
10.1002/anie.201810410
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first example of catalytic insertion/asymmetric Claisen rearrangement tandem reaction of N-sulfonyl-1,2,3-triazoles with allyl alcohol esters was achieved by bimetallic relay catalytic systems involving achiral rhodium salt and chiral N,N'-dioxide-indium(III) complex. This manifold could overcome the limitation of single Rh-II catalysis, providing a straight and facile route to various enantioenriched beta/gamma-amino acid derivatives in high yields (up to 99%) with excellent diastereo- and enantioselectivities (up to >95:5 dr, 98:2 er). Moreover, possible transition state models were proposed to elucidate the origin of chiral induction based on the control experiments and X-ray crystal structure of the catalyst.
引用
收藏
页码:16554 / 16558
页数:5
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