Helvetica chimica acta

An Improved and Versatile Method for the Rapid Synthesis of Aryldihydrobenzofuran Systems by a Boron Tribromide??Mediated Cyclization Reaction

R Detterbeck, M Hesse

Index: Detterbeck, Richard; Hesse, Manfred Helvetica Chimica Acta, 2003 , vol. 86, # 2 p. 343 - 360

Full Text: HTML

Citation Number: 15

Abstract

Abstract Boron tribromide is presented as a highly reactive reagent that simultaneously allows the demethylation and fully diastereoselective cyclization of different precursor molecules, obtained by an aldol-type reaction, to a series of hydroxylated aryldihydrobenzofuran systems in racemic form. The latter are often found as key structures in natural compounds of different classes. Syntheses of educts, which mainly took ...

Related Articles:

Synthesis of (+-)-hexahydropronuciferine and related compounds

[Huffman,J.W.; Opliger,C.E. Journal of Organic Chemistry, 1971 , vol. 36, # 1 p. 111 - 117]

More Articles...