Mechanistic and selectivity investigations into Fe-catalyzed 2, 3-disubstituted azaindole formation from β,β-disubstituted tetrazole-Reference-Cited by-同舟云学术

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Mechanistic and selectivity investigations into Fe-catalyzed 2, 3-disubstituted azaindole formation from β,β-disubstituted tetrazole

Published:2022-01 Issue: Volume:517 Page:112032
ISSN:2468-8231
Container-title:Molecular Catalysis
language:en
Short-container-title:Molecular Catalysis

Author:

Wang Juping,Lin Zijie,Zheng Kangcheng,Xiao Rongxing,Qian Li

Funder

Natural Science Foundation of Guangdong Province

National Supercomputer Centre in Guangzhou

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis

Reference45 articles.

1. Recent advances in the global ring functionalization of 7-azaindoles;Kannaboina;Chem. Commun.,2020

2. Regioselective functionalization of 7-azaindole by controlled annular isomerism: The directed metalation-group dance;Dalziel;Angew. Chem.,2019

3. Palladium-catalyzed amination of N-free 2-chloro-7-azaindole;Plas;Org. Lett.,2015

4. Development of potent Pf CLK3 inhibitors based on TCMDC-135051 as a new class of antimalarials;Mahindra;J. Med. Chem.,2020

5. Iridium-catalyzed C3-selective asymmetric allylation of 7-azaindoles with secondary allylic alcohols;Sawano;Chem. Commun.,2021

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