Regio- and enantioselective formation of tetrazole-bearing quaternary stereocenters via palladium-catalyzed allylic amination-Reference-Cited by-同舟云学术

Regio- and enantioselective formation of tetrazole-bearing quaternary stereocenters via palladium-catalyzed allylic amination

Published:2022 Issue:2 Volume:9 Page:456-461
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Khan Shahid¹,Wang Yu¹,Zhang Mei-Na¹,Perveen Shahida¹,Zhang Junjie¹,Khan Ajmal¹^ORCID

Affiliation:

1. Department of Chemistry, School of Chemistry, Xi'an Key Laboratory of Sustainable Energy Materials Chemistry and MOE Key Laboratory for Non-equilibrium Synthesis and Modulation of Condensed Matter, Xi'an Jiao Tong University, Xi'an 710049, P. R. China

Abstract

A general and efficient method via catalysis by readily available Pd(0)/DACH-naphthyl catalyst under mild conditions, unlocks a new platform that permits the synthesis of elusive quaternary N2-allylic tetrazoles, even in the context of late-stage functionalization.

Funder

Central University Basic Research Fund of China

Xi'an Municipal Bureau of Science and Technology

Xi’an Jiaotong University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D1QO01648B

Reference63 articles.

1. Tetrazoles via Multicomponent Reactions