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Volumn 14, Issue 7, 2016, Pages 2327-2346
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4R- and 4S-iodophenyl hydroxyproline, 4R-pentynoyl hydroxyproline, and S-propargyl-4-thiolphenylalanine: Conformationally biased and tunable amino acids for bioorthogonal reactions
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACIDS;
AROMATIC COMPOUNDS;
CHEMICAL BONDS;
CHEMICAL REACTIONS;
CONFORMATIONS;
FUNCTIONAL GROUPS;
HYDROCARBONS;
PEPTIDES;
PROTEINS;
AROMATIC AMINO ACID;
BIOLOGICAL MOLECULE;
BIOORTHOGONAL REACTIONS;
CONFORMATIONAL PREFERENCES;
CROSS COUPLING REACTIONS;
FUNCTIONALIZATIONS;
MEDICINAL CHEMISTRY;
SONOGASHIRA REACTIONS;
HYDROXYPROLINE;
ALANINE;
FORMIC ACID DERIVATIVE;
HYDROXYPROLINE;
IODINE;
PEPTIDE;
PHENYLACETIC ACID DERIVATIVE;
T-BUTYLOXYCARBONYL GROUP;
THIOPHENYL ACETATE;
CHEMISTRY;
CONFORMATION;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
SYNTHESIS;
X RAY CRYSTALLOGRAPHY;
ALANINE;
CRYSTALLOGRAPHY, X-RAY;
FORMIC ACID ESTERS;
HYDROXYPROLINE;
IODINE;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR CONFORMATION;
PEPTIDES;
PHENYLACETATES;
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EID: 84959036401
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c5ob02473k Document Type: Article |
Times cited : (10)
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References (115)
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