Catalyst-free C–N bond formation under biocompatible reaction conditions-Reference-Cited by-同舟云学术

Catalyst-free C–N bond formation under biocompatible reaction conditions

Published:2022 Issue:8 Volume:24 Page:3321-3325
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Goh Jeffrey¹^ORCID,Ong Seng Kheong¹^ORCID,Tan Yan Sheng¹,Loh Teck-Peng¹²^ORCID

Affiliation:

1. Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 637371 Singapore

2. Henan University of Technology, 100 Lianhua St, Zhongyuan District, Zhengzhou, Henan, 450001, China

Abstract

A C–N bond formation reaction under benign conditions for the amination of allenic ketones to access enaminones is reported. This reaction is atom economical, green, highly regioselective and works well with many structurally crucial amines.

Funder

Nanyang Technological University

Ministry of Education - Singapore

Agency for Science, Technology and Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/GC/D2GC00027J

Reference23 articles.

1. Evaluation of the antinociceptive activities of enaminone compounds on the formalin and hot plate tests in mice

2. Design, synthesis and anticonvulsant evaluation of fluorinated benzyl amino enaminones

3. Enaminones as building blocks in drug development: Recent advances in their chemistry, synthesis, and biological properties

4. Water-Accelerated Aldol Reaction of Ketene Silyl Acetals with Carbonyl Compounds

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