Synthesis 1988; 1988(6): 486-488
DOI: 10.1055/s-1988-27619
communication
© 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.

Synthesis of Six-Membered Heterocycles via the Ring Cleavage of α-Bromo-γ-butyrolactone Promoted by Organotin Alkoxide

Ikuya Shibata* , Mitsuki Toyota, Akio Baba, Haruo Matsuda
  • *Department of Applied Chemistry, Faculty of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565, Japan
Further Information

Publication History

Publication Date:
20 August 2002 (online)

Novel six-membered heterocyclic compounds, such as tetrahydro-1,3-oxazin-2-ones 10a-e, 2-imino-1,3-oxathiane (11), and tetrahydro-2-imino-1,3-oxazine (12) are prepared by the ring cleavage of α-bromo-γ-butyrolactone, promoted by organotin alkoxide.

    >