A general sultone route to the pamamycin macrodiolides - Total synthesis of pamamycin-621A and pamamycin-635B

Angewandte Chemie - International Edition

Volumn 44, Issue 38, 2005, Pages 6231-6234

  Fischer, Petra ^a   Segovia, Ana Belén García ^a   Gruner, Margit ^a   Metz, Peter ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

Antibiotics; Domino reactions; Natural products; Sulfur heterocycles; Total synthesis

Indexed keywords

DOMINO REACTIONS; EPIMERIZATION; NATURAL PRODUCTS; SULFUR HETEROCYCLES; TOTAL SYNTHESIS;

ANTIBIOTICS; ESTERS; OXYGEN; SUBSTITUTION REACTIONS; SULFUR;

SYNTHESIS (CHEMICAL);

ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; MACROLIDE; ORGANIC COMPOUND; PAMAMYCIN;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ANTI-BACTERIAL AGENTS; ANTIBIOTICS, ANTIFUNGAL; ANTIFUNGAL AGENTS; MACROLIDES; MOLECULAR STRUCTURE; ORGANIC CHEMICALS; STEREOISOMERISM;

EID: 25844469497     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200501511     Document Type: Article

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