Intramolecular alder-ene reaction of 2-methyl-4-(alkynyloxy)cyclohexa-2,5-dienones: catalyst-free access to hydrobenzofuran derivatives

TitleIntramolecular alder-ene reaction of 2-methyl-4-(alkynyloxy)cyclohexa-2,5-dienones: catalyst-free access to hydrobenzofuran derivatives
Publication TypeJournal Article
Year of Publication2026
AuthorsRai, A, Bajpai, P, Kundu, AI, Vanka, K, Das, U
JournalOrganic Letters
Volume28
Issue16
Pagination5195-5199
Date PublishedAPR
Type of ArticleArticle
ISSN1523-7060
Abstract

An atom-economical intramolecular Alder-ene reaction has been developed to construct hydrobenzofurans via the direct coupling of an allylic hydrogen atom to an alkyne. This transformation delivers hydrobenzofuran and hydroindole scaffolds in a single step, incorporating all atoms of the starting materials and exemplifying high atom economy. The synthesized products serve as versatile intermediates and exhibit notable reactivity toward further derivatization, as showcased through a range of transformations enabling rapid access to structurally diverse and complex molecules.

DOI10.1021/acs.orglett.6c01057
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

4.6

Divison category: 
Organic Chemistry
Physical and Materials Chemistry
Database: 
Web of Science (WoS)

Add new comment