Amino Acids and Peptides, Volume 23
J H Jones
Royal Society of Chemistry, Jan 1, 1992 - Reference - 349 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
Analytical Studies of Amino Acids
19 other sections not shown
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a-amino acetate activity acylation aldehyde alkylation amide amino acids antagonist Antibiotics azetidinone Biochem Biol Biopolymers bond Bull C-terminal carbapenem carboxylate catalyzed cephalosporins cephem CH2Ph Chea Chem Chem Sor chemistry Chen chiral chloride Chromatogr chymotrypsin complexes compounds conformation copper(II corresponding coupling crystal cyclic peptides deprotection derivatives diastereoisomer diastereoselective dipeptide disulphide enzyme ester Fmoc formation formed fragment gave give glycine hydrolysis imines inhibitors interactions intermediate IntJ.Pept.Protein Res intramolecular involving isomer isostere J.Org.Chem JMed.Chem Khim Kiso ligand metal methods methyl methyl ester moiety molecular molecule nitrogen nucleophile oxidation P-lactam P-turn peptide containing Peptide Protein Res peptide synthesis Perkin Trans Pharm phenylalanine potent precursor prepared presence protecting group Protein racemization reaction Reagents receptor renin reported residues resin ring route Scheme Schiff base side-chain similar SPPS stereoselective structure substituted substrates Synth techniques Tetrahedron Lett yield