An Experimental and Theoretical Study on the Interaction of N-Heterocyclic Carbene-Derived 1,3-Dipoles with Methoxycarbonylallenes: Highly Regio- and Stereoselective [3+2]-Cycloadditions Controlled by the Structures of N-Heterocycles of 1,3-Dipoles-Reference-Cited by-同舟云学术

An Experimental and Theoretical Study on the Interaction of N-Heterocyclic Carbene-Derived 1,3-Dipoles with Methoxycarbonylallenes: Highly Regio- and Stereoselective [3+2]-Cycloadditions Controlled by the Structures of N-Heterocycles of 1,3-Dipoles

Published:2009-02-20 Issue:6 Volume:74 Page:2357-2367
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cheng Ying¹,Wang Bo¹,Wang Xiao-Rong¹,Zhang Jian-Hong¹,Fang De-Cai¹

Affiliation:

1. College of Chemistry, Beijing Normal University, Beijing, 100875, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo802687m

Reference41 articles.

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3. Low-lying stepwise paths for ethylene 1,3-dipolar cycloadditions: A DFT study

4. Assessment of mechanistic hypotheses of 1,3-dipolar cycloaddition of (arylsulfonyl)allene to nitrilimines by DFT reactivity indices

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