Base induced rearrangement of an α-bromophosphonamidate: stereochemistry of ring opening of the azaphosphiridine oxide intermediate as revealed by X-ray crystallography-Reference-Cited by-同舟云学术

Base induced rearrangement of an α-bromophosphonamidate: stereochemistry of ring opening of the azaphosphiridine oxide intermediate as revealed by X-ray crystallography

Published:1993 Issue:24 Volume: Page:1826-1828
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Fawcett John,Harger Martin J. P.,Russell David R.,Sreedharan-Menon Ramesh

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930001826

Reference17 articles.

1. Reactions of N-phenyl α-halogenophosphonamidates with alkoxide: migration of the anilino group from phosphorus to the α carbon atom

2. Evidence for cyclic azaphosphiridine oxide intermediates in the methoxide-induced rearrangements of N-alkyl α-chlorophosphonamidates: formation of phosphoramidates as well as α-aminophosphonates

3. Phosphor in Dreiringen

4. Dreigliedrige Heterocyclen Phosphonsäureesterhydrazide durch Alkoholat-induzierte Umlagerung vonN-Chlorphosphonsäurediamiden

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5. Stereochemistry of the methoxide induced rearrangement of an α-bromophosphonamidate: cleavage of the P–N and P–C bonds in the azaphosphiridine oxide intermediate 1;Journal of the Chemical Society, Perkin Transactions 1;1997