Unveiling the intramolecular [3 + 2] cycloaddition reactions of <i>C</i>,<i>N</i>-disubstituted nitrones from the molecular electron density theory perspective-Reference-Cited by-同舟云学术

Unveiling the intramolecular [3 + 2] cycloaddition reactions of C,N-disubstituted nitrones from the molecular electron density theory perspective

Published:2022 Issue:16 Volume:46 Page:7721-7733
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Acharjee Nivedita¹^ORCID,Mondal Asmita¹,Chakraborty Mrinmoy²

Affiliation:

1. Department of Chemistry, Durgapur Government College, Durgapur, 713214, West Bengal, India

2. Department of Electronics and Communication Engineering, Dr B. C. Roy Engineering College, Durgapur, 713206, West Bengal, India

Abstract

The zwitterionic type intramolecular [3 + 2] cycloaddition reactions of nitrones show remarkable substituent effects and varying reactivities in the cases of cyclic and acyclic alkenes.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ00888B

Reference71 articles.

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4. A.Padwa and W. H.Pearson , in Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products , John Wiley & Sons , 2002 , 59

5. Heterocycles from Alkylidenecyclopropanes

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