Synlett 2007(7): 1016-1025  
DOI: 10.1055/s-2007-973894
ACCOUNT
© Georg Thieme Verlag Stuttgart · New York

Domino Reactions of 1,3-Bis(silyl enol ethers) with 4-(Trialkylsilyloxy)benzopyrylium Triflates

Peter Langer*a,b
a Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany
Fax: +49(381)4986412; e-Mail: peter.langer@uni-rostock.de;
b Leibniz-Institut für Katalyse e. V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany
Further Information

Publication History

Received 15 October 2006
Publication Date:
13 April 2007 (online)

Abstract

4-(Silyloxy)benzopyrylium triflates can be readily generated in situ by reaction of chromones with trialkylsilyl-tri­fluoromethanesulfonate. Domino reactions of silyl enol ethers with benzopyrylium triflates - derived from chromones, 3-cyanochromones and 3-formylchromones - allow an efficient synthesis of a variety of carba- and heterocycles.

  • 1 Introduction

  • 2 Reaction of 1,3-Bis(silyl enol ethers) with Chromones

  • 3 Reaction of 1,3-Bis(silyl enol ethers) with 3-Cyanochromones

  • 4 Reaction of 1,3-Bis(silyl enol ethers) with 3-Formylchromones

  • 5 Conclusions