A convergent strategy for the pamamycin macrodiolides: Total synthesis of pamamycin-607, pamamycin-593, and pamamycin-621D precursors

Angewandte Chemie - International Edition

Volumn 46, Issue 37, 2007, Pages 7086-7089

  Lanners, Steve ^a   Norouzi Arasi, Hassan ^a   Salom Roig, Xavier J ^b   Hanquet, Gilles ^a  

^a CNRS   (France)

^b UNIVERSITÉ DE MONTPELLIER   (France)

Author keywords

Aldol reaction; Natural products; Pamamycins; Regioselectivity; Total synthesis

Indexed keywords

ALDOL REACTIONS; NATURAL PRODUCTS; PAMAMYCIN MACRODIOLIDES;

ISOMERIZATION; KETONES; ORGANIC SOLVENTS; REACTION KINETICS; REGIOSELECTIVITY; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

ANTIBIOTICS;

ANTIINFECTIVE AGENT; MACROLIDE; ORGANIC COMPOUND; PAMAMYCIN; PAMAMYCIN 607; PAMAMYCIN-607; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; DRUG DESIGN; NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

ANTI-BACTERIAL AGENTS; DRUG DESIGN; MACROLIDES; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; ORGANIC CHEMICALS;

EID: 34848893572     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200701749     Document Type: Article

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