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-00000084.xml
Synthesis 1988; 1988(9): 735-739
DOI: 10.1055/s-1988-27693
DOI: 10.1055/s-1988-27693
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.
Ein neuartiger Zugang zu Heteroarylmethyl-, Heteroarylethylphosphonsäure-estern und deren freien Säuren
Further Information
Publication History
Publication Date:
18 September 2002 (online)
A Novel Approach to Heteroarylmethyl- and Heteroarylethylphosphonates (Imidazolylmethyl)-, (thiazolylmethyl)-, and (5-oxo-5,6-dihydroimidazo[1,2-c] pyrimidinylmethyl)triphenylphosphonium bromides (2, 3, 4) react with diethyl phosphiteanion or with the carbanion of ethyl diethoxyphosphorylacetate to give the corresponding heteroarylmethyl- or heteroarylphosphonates 5, 6, 8, 10, 12, 13. The free phosphonic acids 7, 8, 11, 14 can be prepared by cleavage with bromotrimethylsilane.