Stereoselective synthesis of β-methoxytyrosine derivatives for identification of the absolute configuration of callipeltin E

Synthesis

Volumn , Issue 23, 2007, Pages 3666-3672

  Konno, Hiroyuki ^a   Aoyama, Sachiyo ^b   Nosaka, Kazuto ^a   Akaji, Kenichi ^a  

^a KYOTO PREFECTURAL UNIVERSITY OF MEDICINE   (Japan)

^b UNIVERSITY OF TOKUSHIMA   (Japan)

Author keywords

Methoxytyrosine; Anti HIV activity; Callipeltin; Cyclodepsipeptide; Marine sponge; Unusual amino acid

Indexed keywords

ANTI-HIV ACTIVITY; CALLIPELTIN; CYCLODEPSIPEPTIDE; MARINE SPONGE;

AMINO ACIDS; ISOMERS; NUCLEAR MAGNETIC RESONANCE; PEPTIDES; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

DERIVATIVES;

AMINO ACID DERIVATIVE; BETA METHOXYTYROSINE DERIVATIVE; CALLIPELTIN E; TYROSINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 37049015362     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-990848     Document Type: Article

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