Extensively stereodiversified scaffolds for use in diversity-oriented library synthesis

Organic Letters

Volumn 5, Issue 5, 2003, Pages 621-624

  Gierasch, Tiffany Malinky ^a   Shi, Zhangjie ^a   Verdine, Gregory L ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE; MU OPIATE RECEPTOR; SILICON DIOXIDE; SYNTHETIC PEPTIDE; ALCOHOL DERIVATIVE; ALKENE; AMINO ACID; FLUORENE DERIVATIVE; FORMIC ACID DERIVATIVE; LEUCINE; N(ALPHA) FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS; N(ALPHA)-FLUORENYLMETHYLOXYCARBONYLAMINO ACIDS; OLIGOPEPTIDE; T BUTYLOXYCARBONYL GROUP; T-BUTYLOXYCARBONYL GROUP;

AMINO ACID SEQUENCE; AMINO TERMINAL SEQUENCE; ARTICLE; CARBOXY TERMINAL SEQUENCE; CLAISEN CONDENSATION; DRUG BINDING SITE; DRUG PROTEIN BINDING; DRUG SYNTHESIS; ENANTIOSELECTIVITY; GEL CHROMATOGRAPHY; GEOMETRY; HYDROPHOBICITY; NUCLEAR MAGNETIC RESONANCE; PEPTIDE ANALYSIS; PEPTIDE SYNTHESIS; RING CLOSING METATHESIS; STEREOCHEMISTRY; STEREOISOMERISM; WOLFF REARRANGEMENT; CHEMISTRY; COMBINATORIAL CHEMISTRY; METHODOLOGY; SYNTHESIS;

ALCOHOLS; ALKENES; AMINO ACIDS; COMBINATORIAL CHEMISTRY TECHNIQUES; FLUORENES; FORMIC ACID ESTERS; LEUCINE; OLIGOPEPTIDES; STEREOISOMERISM;

EID: 0037529216     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol027116f     Document Type: Article

References (32)

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