SEPARATION OF STEREOISOMERIC 1,1'-BIS(ALPHA-HYDROXYETHYL)FERROCENES BY LIPASE-MEDIATED ACETYLATION IN ORGANIC-SOLVENT
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LAMBUSTA, D
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CNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALYCNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALY
LAMBUSTA, D
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NICOLOSI, G
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CNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALYCNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALY
NICOLOSI, G
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PATTI, A
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CNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALYCNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALY
PATTI, A
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PIATTELLI, M
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CNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALYCNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALY
PIATTELLI, M
[1
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[1] CNR, IST STUDIO SOSTANZE NAT INTERESSE ALIMENTARE & CHI, VIA SANTUARIO 110, I-95028 VALVERDE, ITALY
Acetylation of meso,dl-1,1'-bis(alpha-hydroxyethyl)ferrocene in dry acetone using vinyl acetate as acetyl donor and Pseudomonas cepacia lipase as catalyst allowed the diacetate of the (R,R)-enantiomer and the free (S,S)-diol to be obtained. A concurrent desymmetrization of the meso-diol was also obtained.