Electrophile-Induced Reactions of Cross-Conjugated Enynones in the Synthesis of Heterocycles

Research outputpeer-review

1 Citation (Scopus)

Abstract

[Figure not available: see fulltext.] Being compounds with multiple electrophilic centers, cross-conjugated enynones can be involved in various transformations upon treatment with electrophiles, in particular, Lewis and Brønsted acids, providing a convenient access to acyclic and cyclic compounds. This review covers literature data on electrophile-assisted reactions of substrates with cross-conjugated enynone scaffold toward the synthesis of heterocyclic compounds. The information is arranged according to the type of enynone motif, and chemical transformations of 2-(alkyn-1-yl)alk-2-en-1-ones and alk-1-en-4-yn-3-ones are discussed. The bibliography includes 52 sources.

Original languageEnglish
Pages (from-to)829-836
JournalChemistry of Heterocyclic Compounds
Volume56
DOIs
Publication statusPublished - 20 Aug 2020

Scopus subject areas

  • Organic Chemistry

Fingerprint Dive into the research topics of 'Electrophile-Induced Reactions of Cross-Conjugated Enynones in the Synthesis of Heterocycles'. Together they form a unique fingerprint.

Cite this