Efficient syntheses of geodiamolide A and jaspamide, cytotoxic and antifungal cyclic depsipeptides of marine sponge origin

Tetrahedron Letters

Volumn 35, Issue 4, 1994, Pages 591-594

  Imaeda, Takayuki ^a   Hamada, Yasumasa ^a   Shioiri, Takayuki ^a  

^a NAGOYA CITY UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIFUNGAL AGENT; CYTOTOXIC AGENT; DEPSIPEPTIDE; GEODIAMOLIDE A; JASPAMIDE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; METHODOLOGY; REACTION ANALYSIS;

EID: 0028256250     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)75846-1     Document Type: Article

References (23)

1. Routes to the Tripeptide Unit of Geodiamoude-A
2. Stereocontrolled Synthesis of the Non-Peptide C1-C9 Segment of Jaspamide and Geodiamolides
3. Convergent, enantiospecific total synthesis of the novel cyclodepsipeptide (+)-jasplakinolide (jaspamide)
4. N-Methylamino Acids in Peptide Synthesis. II. A New Synthesis ofN-Benzyloxycarbonyl,N-Methylamino Acids
5. N-Methylamino acids in peptide synthesis. V. The synthesis ofN-tert-butyloxycarbonyl,N-methylamino acids byN-methylation