STUDY OF INTRAMOLECULAR STAUDINGER REACTION AND REDUCTIVE CYCLIZATIONIN 4-ALKOXY-1,3,2-OXAZA-PHOSPHORINANE RING FORMATION - SYNTHESIS OF BICYCLIC PREACTIVATED ANALOGS OF CYCLOPHOSPHAMIDE

Authors
LILO B FAUS L BOUCHU D
Citation
B. Lilo et al., STUDY OF INTRAMOLECULAR STAUDINGER REACTION AND REDUCTIVE CYCLIZATIONIN 4-ALKOXY-1,3,2-OXAZA-PHOSPHORINANE RING FORMATION - SYNTHESIS OF BICYCLIC PREACTIVATED ANALOGS OF CYCLOPHOSPHAMIDE, Phosphorus, sulfur and silicon and the related elements, 75(1-4), 1993, pp. 171-174
Citations number
8
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Phosphorus, sulfur and silicon and the related elements → ACNP
ISSN journal
10426507
Volume
75
Issue
1-4
Year of publication
1993
Pages
171 - 174
Database
ISI
SICI code
1042-6507(1993)75:1-4<171:SOISRA>2.0.ZU;2-E
Abstract
The synthesis of 4-alkoxy-1,3,2-oxaza-phosphorinanes in the oxo-2-aza- 4,9-dioxa-3-phosphabicyclo-(4.3.0)nonane and xo-2-aza-4,10-dioxa-3-pho sphabicyclo-(4.4.0)decane series has been performed starting from azid oalcohols using intramolecular Staudinger reaction and reductive cycli sation.