Reaction mechanisms in peptide synthesis. Part 1. Semiquantitative characteristics of the reactivity of 2-methyl-5(4H)-oxazolone with water and ammonia in the gas phase and weakly polar media-Reference-Cited by-同舟云学术

Reaction mechanisms in peptide synthesis. Part 1. Semiquantitative characteristics of the reactivity of 2-methyl-5(4H)-oxazolone with water and ammonia in the gas phase and weakly polar media

Published:1991-12 Issue:6 Volume:5 Page:585-597
ISSN:0920-654X
Container-title:Journal of Computer-Aided Molecular Design
language:en
Short-container-title:J Computer-Aided Mol Des

Author:

Ciarkowski Jerzy,Chen Francis M. F.,Benoiton N. Leo

Publisher

Springer Science and Business Media LLC

Subject

Physical and Theoretical Chemistry,Computer Science Applications,Drug Discovery

Link

http://link.springer.com/content/pdf/10.1007/BF00135316.pdf

Reference27 articles.

1. Bodanszky, M., Klausner, Y.S. and Ondetti, M.A., Peptide Synthesis, 2nd ed., Interscience, New York, NY, 1976, pp. 85?136.

2. Kemp, D.S., In Gross, E. and Meienhofer, J. (Eds.) The Peptides, Vol. 1 (Analysis, Synthesis, Biology), Academic Press, New York, NY, 1979, pp. 315?383.

3. Benoiton, N.L., Kemp, D.S., In Gross, E. and Meienhofer, J. (Eds.) The Peptides, Vol. 5 (Analysis, Synthesis, Biology), Academic Press, New York, NY, 1983, pp. 217?284.

4. Chen, F.M.F., Kuroda, K. and Benoiton, N.L., Synthesis (1979) 230.

5. Chen, F.M.F., Kuroda, K. and Benoiton, N.L., Synthesis (1978) 928.

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Peptide conjugation: unexpected ring opening of azacrown ether nucleophiles in the oxazolone-based coupling;Chemical Communications;2001

2. Reactive Intermediates in Peptide Synthesis: First Crystal Structures and ab Initio Calculations of 2-Alkoxy-5(4H)-oxazolones from Urethane-Protected Amino Acids;Journal of the American Chemical Society;1997-05-01

3. Mixed anhydride reactivity by means of the molecular orbital AM1 and PM3 methods;Peptides 1994;1995

4. Reaction mechanisms in peptide synthesis. Part 2. Tautomerism of the peptide bond;Journal of Computer-Aided Molecular Design;1991-12