114693-83-3Relevant articles and documents
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Mironov,V.A. et al.
, (1973)
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Chemoenzymatic synthesis of both enantiomers of 3-hydroxy-2,2- dimethylcyclohexanone
Chenevert, Robert,Levesque, Carine,Morin, Pierre
supporting information; experimental part, p. 9501 - 9503 (2009/04/06)
(Chemical Equation Presented) The stereoselective acetylation of meso-2,2-dimethyl-1,3-cyclohexanediol by vinyl acetate in the presence of three lipases gave the (1R,3S)-monoester in high enantiomeric excess (ee ≥ 98%). The hydrolysis of the corresponding meso-diacetate in the presence of Candida antarctica lipase in phosphate buffer provided the opposite enantiomer. Optically active monoacetates were converted to both enantiomers of 3-hydroxy-2,2-dimethylcyclohexanone, a versatile chiral building block.
Elektroreduktion organischer Verbindungen, 14. Die elektrochemische Reduktion von 1,3-Bis(methansulfonyloxy)cyclohexanen.
Hoffmann, Joachim,Holst, Hartmut,Volz, Wolfgang,Voss, Juergen
, p. 401 - 428 (2007/10/02)
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