Phospholidines incorporating a β N-sulfonylaminoalcohol moiety: first observed selectivity of phosphorus heterocycle aminolysis in the presence of water-Reference-Cited by-同舟云学术

Phospholidines incorporating a β N-sulfonylaminoalcohol moiety: first observed selectivity of phosphorus heterocycle aminolysis in the presence of water

Published:2005 Issue:2 Volume:3 Page:227-232
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Dujols Frédéric,Marty Laurence,Mulliez Michel

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2005/OB/B415285A

Reference27 articles.

1. Etude d'un schema de synthese peptidique intramoleculaire a l'aide de derives du phosphore tetraedrique

2. Cyclic phosphonic-carboxylic imides and anhydrides as reactive intermediates. 1. Rearrangement and solvolysis of N-(amino(methyl)phosphinyl)-L-phenylalanine derivatives

3. REACTIONS DES DIOXO-2,4 ET OXO-4 THIOXO-2 DIAZAPHOSPHOLIDINES-1,3,2 AVEC DIVERS NUCLEOPHILES

4. Catalyse Intramoleculaire De L'Aminolyse D'Heterocycles Phosphores Derives Des α Aminoamides. I: Synthese De (Thio) Phosphor(N)Diamides Incorporant Un Residu De ß Aminoacide

5. Intramolecular catalysis of aminolysis of phosphorus heterocycles incorporating an α-aminoamide moiety. III. Synthesis of 2-oxo or 2-thioxo 1,3-disulfonyl-1,3,2-diazaphospholidines and reactions with amines and alcohols

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