Published in

Elsevier, Tetrahedron Letters, 25(49), p. 4007-4010

DOI: 10.1016/j.tetlet.2008.04.090

Links

Tools

Export citation

Search in Google Scholar

Enantiodivergent synthesis of trans-3,4-disubstituted succinimides by SmI2-mediated Reformatsky-type reaction

Journal article published in 2008 by Geng-Jie Lin, 黄培强, Shi-Peng Luo, Xiao Zheng, Jian-Liang Ye, Pei-Qiang Huang ORCID
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Upload
Red circle
Postprint: archiving forbidden
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

An enantiodivergent strategy for the synthesis of traps-3,4-disubstituted succinimides is reported. The key step is a highly trans-stereoselective SmI2-induced Reformatsky-type reaction of 4-substituted-O-benzoylated malimides with carbonyl compounds. Double chirality transmissions were performed with good to excellent diastereoselectivities. (C) 2008 Elsevier Ltd. All rights reserved.