The browser you are using is not supported by this website. All versions of Internet Explorer are no longer supported, either by us or Microsoft (read more here: https://www.microsoft.com/en-us/microsoft-365/windows/end-of-ie-support).

Please use a modern browser to fully experience our website, such as the newest versions of Edge, Chrome, Firefox or Safari etc.

Diastereoselective formation of 2,3,4,5-tetrasubstituted tetrahydrofurans by a Lewis acid promoted addition of C3-substituted 1,3-bis(silyl)propenes to aldehydes

Author

Summary, in English

A mild, efficient, Lewis acid promoted addition of C3-substituted 1,3-bis(silyl)propenes to aldehydes to provide the corresponding 2,3,4,5-tetrasubstituted tetrahydrofurans in excellent stereoselectivity is reported. (C) 2013 Elsevier Ltd. All rights reserved.

Publishing year

2013

Language

English

Pages

3916-3918

Publication/Series

Tetrahedron Letters

Volume

54

Issue

30

Document type

Journal article

Publisher

Elsevier

Topic

  • Chemical Sciences

Keywords

  • Tetrahydrofuran
  • Allylsilanes
  • Diastereoselectivity
  • Lewis acid
  • Aldehyde

Status

Published

ISBN/ISSN/Other

  • ISSN: 0040-4039