85440-70-6Relevant articles and documents
Highly enantioselective transformations on 3,4-dihydroxytetrahydrofurans catalyzed by lipases
Recuero, Veronica,Brieva, Rosario,Gotor, Vicente
, p. 1684 - 1688 (2008/12/21)
Enzymatic acylations and alkoxycarbonylations of cis- and trans-3,4-dihydroxytetrahydrofuran and hydrolysis of their diacetylated and dialkoxycarbonylated derivatives have been studied. High enantioselectivity is obtained using Pseudomonas cepacia lipase as a catalyst in the hydrolysis of the trans-diacetyl derivative, while for the desymmetrization of the cis-3,4-dihydroxytetrahydrofuran the best results are obtained in the acylation process catalyzed by Candida antarctica lipase B.
SYNTHESIS AND PHYSICOCHEMICAL PROPERTIES OF CIS- AND TRANS-OXOLANE-3,4-DIOL DERIVATIVES
Eremenko, L. T.,Korolev, A. M.,Berezina, L. I.,Kirpichev, E. P.,Rubtsov, Yu. I.,Sorokina, T. V.
, p. 795 - 798 (2007/10/02)
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