Construction of Fused Pyrrolidines and β-Lactones by Carbene-Catalyzed C-N, C-C, and C-O Bond Formations

被引:55
作者
Wu, Xingxing [1 ]
Hao, Lin [1 ]
Zhang, Yuexia [1 ]
Rakesh, Maiti [1 ]
Reddi, Rambabu N. [1 ]
Yang, Song [2 ]
Song, Bao-An [2 ]
Chi, Yonggui Robin [1 ,2 ]
机构
[1] Nanyang Technol Univ, Div Chem & Biol Chem, Sch Phys & Math Sci, Singapore 637371, Singapore
[2] Guizhou Univ, Minist Educ, Key Lab Green Pesticide & Agr Bioengn, Lab Breeding Base Green Pesticide & Agr Bioengn, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金; 新加坡国家研究基金会;
关键词
heterocycles; lactones; N-heterocyclic carbenes; organocatalysis; reaction mechanisms; HETEROCYCLIC CARBENE; ENANTIOSELECTIVE SYNTHESIS; ASYMMETRIC-SYNTHESIS; ALPHA; BETA-UNSATURATED ALDEHYDES; COOPERATIVE CATALYSIS; ANNULATION REACTION; DYOTROPIC REARRANGEMENTS; GAMMA-BUTYROLACTONES; ALDOL-LACTONIZATION; MICHAEL ADDITION;
D O I
10.1002/anie.201700045
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A carbene-catalyzed intermolecular C-N bond formation, which initiates a highly selective cascade reaction for the synthesis of pyrrolidine fused beta-lactones, is disclosed. The nitrogen-containing bicyclic beta-lactone products are obtained with good yields and excellent stereoselectivities. Synthetic transformations of the reaction products into useful functional molecules, such as amino catalysts, can be efficiently realized under mild reaction conditions. Mechanistically, this study provides insights into modulating the reactivities of heteroatoms, such as nitrogen atoms, in challenging carbene-catalyzed asymmetric carbon-heteroatom bond-forming reactions.
引用
收藏
页码:4201 / 4205
页数:5
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