Silica-Immobilized Chiral Dirhodium(II) Catalyst for Enantioselective Carbenoid Reactions

被引:63
作者
Chepiga, Kathryn M. [1 ]
Feng, Yan [2 ]
Brunelli, Nicholas A. [2 ]
Jones, Christopher W. [2 ]
Davies, Huw M. L. [1 ]
机构
[1] Emory Univ, Dept Chem, Atlanta, GA 30322 USA
[2] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
C-H ACTIVATION; ASYMMETRIC DIHYDROXYLATION; DONOR/ACCEPTOR CARBENOIDS; TANDEM YLIDE; REARRANGEMENT; CYCLOPROPANATION; SCOPE; FUNCTIONALIZATION; INSERTION; STRATEGY;
D O I
10.1021/ol403006r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A silica-supported dirhodium(II)tetraprolinate catalyst was synthesized in four steps from L-proline and used in a range of enantioselective transformations of donor/acceptor carbenoids. These include cyclopropenation, cyclopropanation, tandem ylide formation/[2,3] sigmatropic rearrangement, and a variety of combined C-H functionalization/Cope rearrangement reactions. The products of these transformations were obtained in yields and levels of enantioselectivity comparable to those obtained with its homogeneous counterpart, Rh-2(S-DOSP)(4). The silica-supported Rh-2(S-DOSP)(4) derivative was successfully recycled over five reactions.
引用
收藏
页码:6136 / 6139
页数:4
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