Synthetic study towards azadirachtin: An efficient and stereoselective construction of the AB rings with full functionality

Angewandte Chemie - International Edition

Volumn 46, Issue 9, 2007, Pages 1512-1516

  Watanabe, Hidenori ^a   Mori, Naoki ^a   Itoh, Daisuke ^a   Kitahara, Takeshi ^a,b   Mori, Kenji ^a,c  

^a UNIVERSITY OF TOKYO   (Japan)

^b KITASATO INSTITUTE   (Japan)

^c INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

Author keywords

Claisen rearrangement; Diels Alder reaction; Natural products; Radical reactions

Indexed keywords

CYCLIZATION; REACTION KINETICS; STEREOSELECTIVITY;

AZADIRACHTIN; CLAISEN REARRANGEMENT; DIELS-ALDER REACTION; NATURAL PRODUCTS; RADICAL REACTIONS;

ORGANIC COMPOUNDS;

AZADIRACHTIN; LIMONOID;

ARTICLE; AZADIRACHTA INDICA; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

AZADIRACHTA; LIMONINS; MODELS, CHEMICAL; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 34247873121     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200604097     Document Type: Article

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