Regio- and stereoselectivity of the 1,3-dipolar cycloaddition of azomethine ylides to (E)-3-(2-oxo-2-(pyren-1-yl)ethylidene)indolin-2-ones: A combined experimental and theoretical study-Reference-Cited by-同舟云学术

Regio- and stereoselectivity of the 1,3-dipolar cycloaddition of azomethine ylides to (E)-3-(2-oxo-2-(pyren-1-yl)ethylidene)indolin-2-ones: A combined experimental and theoretical study

Published:2022-06 Issue:6 Volume:15 Page:103855
ISSN:1878-5352
Container-title:Arabian Journal of Chemistry
language:en
Short-container-title:Arabian Journal of Chemistry

Author:

Hussein Essam M.,Moussa Ziad,Pal Uttam,Alsantali Reem I.,Alzahrani Abdullah Y.A.,Obaid Rami J.,Alzahrani Fawaz M.,Al-Rooqi Munirah M.,Alsharif Meshari A.,El Guesmi Nizar,Jassas Rabab S.,Shaheer Malik M.,Altass Hatem M.,Pal Samir K.,Saha Dasgupta Tanusri,Ahmed Saleh A.

Publisher

Elsevier BV

Subject

General Chemical Engineering,General Chemistry

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1. Study on Regio- and Diastereoselectivity of the 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylide with 2-(Benzo[d]thiazol-2-yl)-3-(aryl)acrylonitrile: Synthesis, Spectroscopic, and Computational Approach;ACS Omega;2024-05-21

2. Spectroscopic, computational and mechanistic studies on regio- and stereoselectivity of the 1,3-dipolar cycloaddition reaction in the synthesis of dispiro[indoline-3,2′-pyrrolidine-3′,3"-indolines] festooned with pyrene moiety;Journal of Molecular Structure;2022-09