Amino Acids and Peptides, Volume 24
J S Davies
Royal Society of Chemistry, Mar 31, 1993 - Reference - 400 pages
Specialist Periodical Reports provide systematic and detailed review coverage of progress in the major areas of chemical research. Written by experts in their specialist fields the series creates a unique service for the active research chemist, supplying regular critical in-depth accounts of progress in particular areas of chemistry. For over 80 years the Royal Society of Chemistry and its predecessor, the Chemical Society, have been publishing reports charting developments in chemistry, which originally took the form of Annual Reports. However, by 1967 the whole spectrum of chemistry could no longer be contained within one volume and the series Specialist Periodical Reports was born. The Annual Reports themselves still existed but were divided into two, and subsequently three, volumes covering Inorganic, Organic and Physical Chemistry. For more general coverage of the highlights in chemistry they remain a 'must'. Since that time the SPR series has altered according to the fluctuating degree of activity in various fields of chemistry. Some titles have remained unchanged, while others have altered their emphasis along with their titles; some have been combined under a new name whereas others have had to be discontinued. The current list of Specialist Periodical Reports can be seen on the inside flap of this volume.
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Physicochemical Studies of Amino Acids
Selected Examples of Peptide Synthesis
22 other sections not shown
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a-amino acylation alkylation amide amino acids analogues antagonists antibiotic aqueous aromatic asymmetric asymmetric synthesis Aust.J.Chem azetidinones binding Biochemistry biological activity Biopolymers BocNH bond C-terminal carbapenem carboxylic cephalosporins Chem Chem.Abs Chem.Commun Chem.Pharm.Bull chiral chloride complex compounds conformation coupling Crisma cyclic cycloaddition cyclosporin deprotection derivatives dioxopiperazine dipeptide enantiomer enolates enzyme ester Fmoc formation fragment gives glycine H-bonds homochiral Hruby hydrolysis imine inhibitors Int.J.Pept.Protein Res Int.J.Peptide Protein Res interaction intermediate intramolecular involving ions isomer isostere J.Amer.Chem.Soc J.Chem.Soc J.Chromatogr J.Med.Chem J.Org.Chem J.W. Perich ketene Liebigs Ann.Chem method methyl moiety molecular molecule OSiMe2Bu1 oxidation p-lactam p-turn penicillin Pept.Res peptide potent precursor prepared presence proline protecting groups Protein R.B. Johns racemization RCONH reaction Reagents receptor replaced residues ring Scheme Schiff base sequence serine side chains Slaninova solution spectra SPPS stereoselective structure substituted substrates synthe synthesis Tetrahedron Lett Toniolo trans X-ray yield