Synthesis of Phosphohomoserine Lactone, A New Pseudopeptide Unit
- 1 May 1996
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 26 (9) , 1739-1745
- https://doi.org/10.1080/00397919608002613
Abstract
We describe here the synthesis of the enantiomerically pure phosphohomoserine lactone which will serve as an haptenic structure in catalytic antibody preparation.Keywords
This publication has 10 references indexed in Scilit:
- Peptide Synthesis Catalyzed by an Antibody Containing a Binding Site for Variable Amino AcidsScience, 1994
- Antibody catalysis of peptide bond formation.Proceedings of the National Academy of Sciences, 1994
- Asymmetric synthesis of?-aminophosphonic acidsAmino Acids, 1992
- Synthesis of enantiomerically pure phosphonic analogues of homoserine derivativesTetrahedron: Asymmetry, 1991
- Potent inhibition of pepsin and penicillopepsin by phosphorus-containing peptide analogsThe Journal of Organic Chemistry, 1990
- Catalytic Antibodies with Lipase Activity and R or S Substrate SelectivityScience, 1989
- Catalysis of a stereospecific bimolecular amide synthesis by an antibody.Proceedings of the National Academy of Sciences, 1988
- A Stereospecific Cyclization Catalyzed by an AntibodyScience, 1987
- Selective Chemical Catalysis by an AntibodyScience, 1986
- Transesterification of Diphenyl Phosphonates using the Potassium Fluoride/Crown Ether/Alcohol System; Part 1. Transesterification of Diphenyl 1-(Benzyloxycarbonylamino)-alkanephosphonatesSynthesis, 1982