Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2000; 2000(2): 223-224
DOI: 10.1055/s-2000-6489
DOI: 10.1055/s-2000-6489
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.1,3-Dipolar Cycloaddition Reactions between Stannyl Alkynes and Nitrile Oxides
Further Information
Publication History
Publication Date:
31 December 2000 (online)
PDF Download(opens in new window) Permissions and Reprints(opens in new window) All articles of this category(opens in new window)
1,3-Dipolar cycloaddition reactions between nitrile oxides and stannyl alkynes proceed in a regiospecific manner to afford 4-stannyl isoxazoles in good yields. No reaction is observed for vinyl- or allylstannanes.
isoxazole - dipolar cycloaddition - stannyl alkyne - regiochemistry