Cu(<scp>ii</scp>)-thiophene-2,5-bis(amino-alcohol) mediated asymmetric Aldol reaction and Domino Knoevenagel Michael cyclization: a new highly efficient Lewis acid catalyst-Reference-Cited by-同舟云学术

Cu(ii)-thiophene-2,5-bis(amino-alcohol) mediated asymmetric Aldol reaction and Domino Knoevenagel Michael cyclization: a new highly efficient Lewis acid catalyst

Published:2022 Issue:10 Volume:12 Page:6149-6165
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Al-Majid Abdullah Mohammed¹,Alammari Abdullah Saleh¹,Alshahrani Saeed¹^ORCID,Haukka Matti²^ORCID,Islam Mohammad Shahidul¹^ORCID,Barakat Assem¹^ORCID

Affiliation:

1. Department of Chemistry, College of Science, King Saud University, P. O. Box 2455, Riyadh 11451, Saudi Arabia

2. Department of Chemistry, University of Jyväskylä, P. O. Box 35, FI-40014 Jyväskylä, Finland

Abstract

The highly efficient Lewis acid-catalytic system Cu(ii)-thiophene-2,5-bis(amino-alcohol) has been developed for enantioselective Aldol reaction of isatin derivatives with ketones.

Funder

King Saud University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/RA/D2RA00674J

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