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Volumn 13, Issue 12, 2002, Pages 1237-1239
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Stereoselective synthesis of (2R,3R,4R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A
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Author keywords
[No Author keywords available]
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Indexed keywords
3 HYDROXY 2,4,6 TRIMETHYLHEPTANOIC ACID;
ACETONE;
CALLIPELTIN A;
CYCLODEPSIPEPTIDE;
HEPTANOIC ACID DERIVATIVE;
HYDROXYACID;
PROTEIN HYDROLYSATE;
UNCLASSIFIED DRUG;
ACYLATION;
AMINO TERMINAL SEQUENCE;
ARTICLE;
CHEMICAL STRUCTURE;
ENANTIOSELECTIVITY;
PEPTIDE ANALYSIS;
PEPTIDE SYNTHESIS;
PRIORITY JOURNAL;
PROTEIN STRUCTURE;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOCHEMISTRY;
SYNTHESIS;
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EID: 0037025289
PISSN: 09574166
EISSN: None
Source Type: Journal
DOI: 10.1016/S0957-4166(02)00328-2 Document Type: Article |
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Times cited : (27)
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References (6)
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