Download PDF
Synlett 1996; 1996(3): 234-236
DOI: 10.1055/s-1996-5396
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Versatile Reactivities of Carbonyl Ylids toward Unactivated Alkenes and Heterodipolarophiles, and their Synthetic Use1

Makoto Hojo, Naruyasu Ishibashi, Akira Hosomi*
  • *Department of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305, Japan, Fax +81(298)53-4237; E-mail hosomi@staff.chem.tsukuba.ac.jp
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

Carbonyl ylids, the simplest one of those reported so far, exhibit versatile reactivities toward not only simple alkenes but also nucleophilic ones and a variety of heterodipolarophiles.

carbonyl ylid - [3+2] cycloaddition - tetrahydrofuran - 1,3-elimination - organosilicon compound - lignan synthesis

      >