Recent Development on the Synthesis of Benzo[b]- and Naphtho[b]furans: A Review

Author(s): Halina Kwiecien, Malgorzata Smist, Monika Kowalewska

Journal Name: Current Organic Synthesis

Volume 9 , Issue 4 , 2012


Become EABM
Become Reviewer
Call for Editor

Abstract:

Over the past twenty years benzo- and naphtho[b]furan synthesis has been a widely studied topic, certainly due to the presence of this structural unit in many biologically active compounds. Most of the known methods of the synthesis of these heterocycles are based on an intramolecular cyclization of various open-chain precursors. There are four possible ways of the cyclization and they are based on a formation of appropriate furan bonds: O-C2, C2-C3, C3-b and O-b. The following paper presents these four methods of synthesis of benzo[b]- and naphtho[b]furans which have been developed over the last years.

Keywords: Aldehyde, ketone, acetal, benzo[b]furan, cyclization, formylaryloxyalkanoic acid, allyl phenol, alkynyl phenol, naphtho[b]furan.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 9
ISSUE: 4
Year: 2012
Page: [529 - 560]
Pages: 32
DOI: 10.2174/157017912802651393
Price: $65

Article Metrics

PDF: 13