Reductive cross-coupling of <i>N</i>-acyl pyrazole and nitroarene using tetrahydroxydiboron: synthesis of secondary amides-Reference-Cited by-同舟云学术

Reductive cross-coupling of N-acyl pyrazole and nitroarene using tetrahydroxydiboron: synthesis of secondary amides

Published:2023 Issue:41 Volume:21 Page:8329-8334
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Moon Hayeon¹,Lee Sunwoo¹^ORCID

Affiliation:

1. Department of Chemistry, Chonnam National University, Gwangju, 61186, Republic of Korea

Abstract

Acyl pyrazoles, in the presence of B2(OH)4, efficiently yield amides when reacted with nitro compounds. The method is versatile, tolerates diverse functional groups, and holds promise for diverse organic molecule synthesis.

Funder

National Research Foundation of Korea

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB01040F

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