The Nitrilimine–Alkene Cycloaddition Regioselectivity Rationalized by Density Functional Theory Reactivity Indices-Reference-Cited by-同舟云学术

The Nitrilimine–Alkene Cycloaddition Regioselectivity Rationalized by Density Functional Theory Reactivity Indices

Published:2017-01-26 Issue:2 Volume:22 Page:202
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Molteni Giorgio,Ponti Alessandro^ORCID

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/22/2/202/pdf

Reference37 articles.

1. Historical Note, General Principle and Mechanistic Criteria;Huisgen,1984

2. Synthesis and reactivity of a stable nitrile imine

3. Nitrilimines: Evidence for the Allenic Structure in Solution, Experimental and Ab Initio Studies of the Barrier to Racemization, and First Diastereoselective [3 + 2]-Cycloaddition

4. Nitrile Imines: Matrix Isolation, IR Spectra, Structures, and Rearrangement to Carbodiimides

5. 1,3-Dipolar cycloadditions involving X=Y groups;Bianchi,1977

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