Shedding light on the energetics, regioselectivity, stereoselectivity, and mechanistic aspects of [3 + 2] cycloaddition reaction between azomethine imines and 2‐sulfolene through molecular electron density theory-Reference-Cited by-同舟云学术

Shedding light on the energetics, regioselectivity, stereoselectivity, and mechanistic aspects of [3 + 2] cycloaddition reaction between azomethine imines and 2‐sulfolene through molecular electron density theory

Published:2019-12-11 Issue:4 Volume:33 Page:
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J Phys Org Chem

Author:

Babazadeh Sayyed Mohsen¹,Emamian Saeedreza¹^ORCID

Affiliation:

1. Chemistry Department, Shahrood BranchIslamic Azad University Shahrood Iran

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/poc.4042

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1. TANDEM CONSTRUCTION OF CARBON–CARBON AND CARBON–OXYGEN BONDS IN THE BAYLIS-HILLMAN CHEMISTRY: SYNTHESIS OF FUNCTIONALIZEDdl-BIS-ALLYL ETHERS

2. DABCO-catalyzed [3+2] cycloaddition reactions of azomethine imines with N -aryl maleimides: facile access to dinitrogen-fused heterocycles

3. Structure-activity relationship within a series of pyrazolidinone antibacterial agents. 2. Effect of side-chain modification on in vitro activity and pharmacokinetic parameters

4. Catalyst-Free and Stereoselective Synthesis of N,N-Bicyclic Pyrazolidinone Derivatives

5. Syntheses by Means of 1-Alkylidene- and 1-(Arylalkylidene)-3-pyrazolidoneN,N-Betaines, a New Type of Stable Azomethine Imine

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