An expeditious coumarin synthesis via a "Pseudocycloaddition" between salicylaldehydes and ketene

Sosale Chandrasekhar, Honnaiah Vijay Kumar

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

A variety of salicylaldehydes effected tandem nucleophilic addition onto ketene, leading to corresponding coumarins in good yields under mild conditions. This "pseudocycloaddition" represents a very mild variant of the historic Perkin synthesis of coumarin (which remains of key interest in both perfumery and several emerging areas).

Original languageEnglish (US)
Pages (from-to)232-235
Number of pages4
JournalSynthetic Communications
Volume45
Issue number2
DOIs
StatePublished - Jan 17 2015

Bibliographical note

Funding Information:
We are grateful to University Grants Commission (New Delhi) for generous financial support to H. V. K.

Publisher Copyright:
© 2015 Taylor & Francis Group, LLC.

Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.

Keywords

  • Coumarin
  • Perkin synthesis
  • quinodimethane

Fingerprint

Dive into the research topics of 'An expeditious coumarin synthesis via a "Pseudocycloaddition" between salicylaldehydes and ketene'. Together they form a unique fingerprint.

Cite this