Synthesis of Phosphinopeptides via the Mannich Ligation
Authors:
- 12 May 2007
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 9 (12) , 2257-2260
Abstract
Phosphinopeptides are a class of unnatural peptides containing a tetrahedral phosphorus atom and have potential for use as enzyme inhibitors. A series of phosphinopeptides were synthesized via the Mannich-type reaction of aryldichlorophosphines, aldehydes, and N-protected amino amides or peptide amides and subsequent aminolysis with amino esters or peptide esters. The current method named the Mannich ligation is an efficient route to synthesis of phosphinopeptides through convergent condensation.Keywords
This publication has 3 references indexed in Scilit:
- The preparation of phosphono peptides containing a phosphonamidate bondTetrahedron, 1994
- N-BENZYLOXYAMINO PHOSPHINYL PEPTIDESPhosphorus, Sulfur, and Silicon and the Related Elements, 1991
- Organophosphorus analogues and derivatives of the natural l-aminocarboxylic acid and peptides vii. Enzyme synthesis of phospha-c peptidesTetrahedron, 1991