Potent pincer-zinc catalyzed homogeneous α-alkylation and Friedländer quinoline synthesis reaction of secondary alcohols/ketones with primary alcohols-Reference-Cited by-同舟云学术

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Potent pincer-zinc catalyzed homogeneous α-alkylation and Friedländer quinoline synthesis reaction of secondary alcohols/ketones with primary alcohols

Published:2024 Issue:31 Volume:22 Page:6393-6408
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jana Debashis¹^ORCID,Roy Sima¹^ORCID,Naskar Srijita¹,Halder Supriyo¹,Kanrar Gopal²,Pramanik Kausikisankar¹^ORCID

Affiliation:

1. Department of Chemistry, Jadavpur University, Kolkata 700032, India

2. Department of Chemistry, St. Xavier's College (Autonomous), Kolkata–700016, India

Abstract

Herein, we describe an air- and moisture-stable, homogeneous zinc catalyst stabilised using an electron deficient N^N^N pincer-type ligand.

Funder

University Grants Commission

Council of Scientific and Industrial Research, India

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00988F

Reference94 articles.

1. G.Brachmachari , Bioactive Natural Products: Chemistry and Biology , CRC Press , 2014

2. A.Ricci , Amino Group Chemistry: From Synthesis to the Life Sciences , Wiley-VCH , 2008

3. J.Hartwig , Organotransition Metal Chemistry: From Bonding to Catalysis , University Science Books , 2009

4. Recent Advances in the Friedländer Reaction

5. Transition-Metal-Catalyzed Utilization of Methanol as a C1 Source in Organic Synthesis

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