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Volumn 307, Issue 2, 2002, Pages 202-211
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Improved initial yields in C-terminal sequence analysis by thiohydantoin chemistry using purified diphenylphosphoryl isothiocyanate: NMR evidence for a reaction intermediate in the coupling reaction
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Author keywords
C terminal sequence analysis; Diphenylphosphoryl isothiocyanate; Thiohydantoin
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Indexed keywords
AMINO ACIDS;
CARBOXYLATION;
CHEMICAL BONDS;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
PEPTIDES;
PURIFICATION;
REAGENTS;
C-TERMINAL SEQUENCES;
CARBOXYL GROUPS;
COUPLING MECHANISM;
COUPLING REACTION;
ISOTHIOCYANATES;
REVERSED PHASE HPLC;
SPECTROSCOPIC EVIDENCE;
THIOHYDANTOIN;
REACTION INTERMEDIATES;
AMINO ACID;
BENZENE;
CARBOXYLIC ACID;
DIPHENYLPHOSPHORYL ISOTHIOCYANATE;
ISOTHIOCYANIC ACID DERIVATIVE;
PEPTIDYLTHIOHYDANTOIN DERIVATIVE;
POTASSIUM DERIVATIVE;
POTASSIUM TRIMETHYLSILANOLATE;
PYRIDINE;
THIOHYDANTOIN DERIVATIVE;
UNCLASSIFIED DRUG;
ANALYTIC METHOD;
ARTICLE;
CARBOXY TERMINAL SEQUENCE;
CHEMICAL REACTION;
DERIVATIZATION;
MOLECULAR STABILITY;
PRIORITY JOURNAL;
PROTEIN DEGRADATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
REACTION ANALYSIS;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
SEQUENCE ANALYSIS;
SYNTHESIS;
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EID: 0037102188
PISSN: 00032697
EISSN: None
Source Type: Journal
DOI: 10.1016/S0003-2697(02)00025-8 Document Type: Article |
Times cited : (4)
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References (43)
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