Chemoenzymatic route to both enantiomers of a 1-isopropyl-3a- methyloctahydroinden-4-one derivative: A synthetic intermediate for sesqui- and diterpenoids

Advanced Synthesis and Catalysis

Volumn 347, Issue 7-8, 2005, Pages 1099-1109

  Fujieda, Shigeo ^a   Tomita, Mina ^a   Fuhshuku, Ken Ichi ^a   Ohba, Shigeru ^a   Nishiyama, Shigeru ^a   Sugai, Takeshi ^a  

^a KEIO UNIVERSITY   (Japan)

Author keywords

Chiral building block; Desymmetrization; Prochiral substrate; Terpenoid synthesis; Whole cell biocatalyst; Yeast reduction

Indexed keywords

1 ISOPROPYL 3A METHYLOCTAHYDROINDEN 4 ONE DERIVATIVE; 2 METHYL 2 (4 METHYL 3 OXOPENTYL) 1,3 CYCLOHEXANEDIONE; ACETAL DERIVATIVE; ALCOHOL; AZULENE DERIVATIVE; CARBONYL DERIVATIVE; CYCLOHEXANE DERIVATIVE; DITERPENOID; INDENE DERIVATIVE; KETOL; KETONE DERIVATIVE; SESQUITERPENE DERIVATIVE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BIOCATALYST; CANDIDA; CANDIDA FLORICOLA; CONTROLLED STUDY; DIASTEREOISOMER; ENANTIOMER; ENZYME SYNTHESIS; MICROORGANISM; NONHUMAN; PINACOL REARRANGEMENT; STEREOCHEMISTRY; TORULASPORA DELBRUECKII;

EID: 20544443716     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/adsc.200505034     Document Type: Article

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