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Synthesis of β-Halofurans

Authors :
Alicia Decker
Roman Dembinski
Deepthi Gundapuneni
Yan Li
Source :
Topics in Heterocyclic Chemistry ISBN: 9783642251023
Publication Year :
2011
Publisher :
Springer Berlin Heidelberg, 2011.

Abstract

Furans substituted with halogens at the beta carbon, which is less prone to electrophilic reactions compared to an alpha position, are important intermediates for accessing highly substituted furans. The regioselectivity of the introduction of a halogen plays an important role in their preparation. This review summarizes efforts for the synthesis of β-halofurans (but not benzofurans) as sorted by halogen (iodo, bromo, chloro, and fluoro). This article provides general reaction schemes that were confirmed with multiple examples and are sometimes applicable to other halogens, and selected reactions specific to a particular substrate and a halogen.

Details

ISBN :
978-3-642-25102-3
ISBNs :
9783642251023
Database :
OpenAIRE
Journal :
Topics in Heterocyclic Chemistry ISBN: 9783642251023
Accession number :
edsair.doi...........3eb284828a6e485c4c30edf39cf205e3
Full Text :
https://doi.org/10.1007/7081_2011_57