Enantioselective N-Heterocyclic Carbene Catalyzed Diene Regenerative (4+2) Annulation

被引:25
作者
Levens, Alison [1 ]
Zhang, Changhe [1 ]
Candish, Lisa [1 ]
Forsyth, Craig M. [1 ]
Lupton, David W. [1 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
DIELS-ALDER REACTIONS; ACYL; ORGANOCATALYSTS; PROGRESS; NHCS;
D O I
10.1021/acs.orglett.5b02693
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An enantioselective N-heterocyclic carbene (NHC)-catalyzed diene regenerative (4 + 2) annulation has been achieved through the use of highly nudeophilic morpholinone-derived catalysts. The reaction proceeds with good to excellent yields, high enantioselectivity (most >92% ee), and good diastereoselectivity (most >7:1). The generality of the reaction is high, with 19 examples reported. The utility of the products has been examined with subsequent derivatization in Diels-Alder reactions using electron-poor dienophiles. Furthermore, interception of the proposed beta-lactone intermediate has been achieved, allowing the synthesis of compounds bearing four contiguous stereocenters with high levels of enantio- and diastereoselectivity.
引用
收藏
页码:5332 / 5335
页数:4
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