4.4 Article

An efficient and stereoselective cycloaddition of C-aryl and C-amido nitrones to dimethyl 2-benzylidenecyclopropane-1,1-dicarboxylate

Journal

TETRAHEDRON
Volume 67, Issue 13, Pages 2391-2395

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2011.02.013

Keywords

Methylenecyclopropane; Nitrone; Isoxazolidine; 1,3-Dipolar cycloaddition; Stereoselectivity

Funding

  1. Ministry of Education and Training of Vietnam

Ask authors/readers for more resources

1,3-Dipolar cycloalditions of dimethyl 2-benzylidenecyclopropane-1,1-dicarboxylate and a number of C-aryl or C-amido nitrones proceed with high efficiency and selectivity with the formation of only one isomeric spiral[cyclopropane-1,4-isoxazolidine] cycloadduct. (C) 2011 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available