Syntheses of the hexahydroindene cores of indanomycin and stawamycin by combinations of iridium-catalyzed asymmetric allylic alkylations and intramolecular diels-alder reactions

Chemistry - A European Journal

Volumn 19, Issue 1, 2013, Pages 400-405

  Gärtner, Martin ^a   Satyanarayana, Gedu ^b   Förster, Sebastian ^a   Helmchen, Günter ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b INDIAN INSTITUTE OF TECHNOLOGY HYDERABAD   (India)

Author keywords

alkylation; Diels Alder reaction; hexahydroindenes; iridium; Julia olefination; Suzuki Miyaura coupling

Indexed keywords

ALLYLIC ALKYLATION; ASYMMETRIC ALLYLIC ALKYLATIONS; CONCISE SYNTHESIS; DIELS-ALDER REACTION; HEXAHYDROINDENES; INTRAMOLECULAR DIELS-ALDER REACTION; JULIA OLEFINATION; SUZUKI-MIYAURA COUPLING;

ALKYLATION; CATALYSIS;

IRIDIUM;

ALLYL COMPOUND; ANTIINFECTIVE AGENT; INDANOMYCIN; INDENE DERIVATIVE; IRIDIUM; ORGANOMETALLIC COMPOUND; PYRAN DERIVATIVE;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

ALKYLATION; ALLYL COMPOUNDS; ANTI-BACTERIAL AGENTS; CATALYSIS; INDENES; IRIDIUM; MOLECULAR STRUCTURE; ORGANOMETALLIC COMPOUNDS; PYRANS; STEREOISOMERISM;

EID: 84871584820     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202822     Document Type: Article

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