An efficient protocol for the enantioselective preparation of a key polyfunctionalized cyclohexane. New access to (R)- and (S)-4-hydroxy-2- cyclohexenone and (R)- and (S)-trans-cyclohex-2-ene-1,4-diol

Journal of Organic Chemistry

Volumn 73, Issue 9, 2008, Pages 3486-3491

  Bayón, Pau ^a   Marjanet, Georgina ^a   Toribio, Gladis ^a   Alibés, Ramon ^a   De March, Pere ^a   Figueredo, Marta ^a   Font, Josep ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; ALCOHOLS; CATALYSIS; ENANTIOSELECTIVITY; ETHYLENE GLYCOL; SYNTHESIS (CHEMICAL);

MULTIGRAM QUANTITIES; POLYFUNCTIONALIZED CYCLOHEXANE;

CYCLOHEXANE;

2 CYCLOHEXENONE; CYCLOHEXANE DERIVATIVE; LIPASE B;

ACETYLATION; ARTICLE; CANDIDA ANTARCTICA; CATALYSIS; ENANTIOSELECTIVITY; NONHUMAN; SYNTHESIS;

ACETYLATION; CANDIDA ALBICANS; CATALYSIS; CYCLOHEXANES; CYCLOHEXANOLS; CYCLOHEXANONES; LIPASE; MOLECULAR STRUCTURE; SOLUBILITY; STEREOISOMERISM;

EID: 43449123330     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800107h     Document Type: Article

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