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Synthesis of propargylamine: pioneering a green path with non-conventional KA2 coupling approach.
Khadanga, Lambodar; Roopan, Selvaraj Mohana.
Affiliation
  • Khadanga L; Chemistry of Heterocycles and Natural Product Research Laboratory, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, Tamil Nadu, 632 014, India.
  • Roopan SM; Chemistry of Heterocycles and Natural Product Research Laboratory, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore, Tamil Nadu, 632 014, India. mohanaroopan.s@vit.ac.in.
Mol Divers ; 2024 Apr 30.
Article in En | MEDLINE | ID: mdl-38687398
ABSTRACT
The KA2 coupling reaction is a well-explored and versatile method for forming C-C bonds in synthetic chemistry. It is composed of ketone, amine, and alkyne, which play a major role in the synthesis of propargylamines, known for their diverse biological activities and are used in treating neurogenetical disorders. The KA2 coupling is highly challenging due to the low reactivity of ketimines toward nucleophilic attacks with metal acetylide intermediates formed by activating the C-H bond of the alkyne. Despite predominant studies conducted on thermal conditions for KA2 coupling reactions, green and sustainable approaches like non-conventional methods still have a lot to achieve. This review article provides a comprehensive introduction to the non-conventional approach in the KA2 coupling reaction, outlining its mechanisms and exploring future aspects.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Divers / Mol. divers / Molecular diversity Journal subject: BIOLOGIA MOLECULAR Year: 2024 Type: Article Affiliation country: India

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Divers / Mol. divers / Molecular diversity Journal subject: BIOLOGIA MOLECULAR Year: 2024 Type: Article Affiliation country: India