enantio-

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enantio-

a combining form meaning “opposite,” “opposing”: enantiomorph.

[< Greek, comb. form of enantíos. See en-², anti-]

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(2015) A novel highly enantio- and diastereoselective synthesis of vitamin E side-chain.

Catalytic enantioselective synthesis of chiral organic compounds of ultra-high purity of >99% ee

Los experimentos fueron realizados de acuerdo con lo descrito en la seccion de materiales y metodos Biocatalizador pH 5 pH 7 Enantio- E (a) Enantio- preferencia preferencia OC-CALB R 11.2 [+ o -] 0.2 R OC-CAL-EDA R 7.3 [+ o -] 0.1 R OC-CALB-TNBS R 16.2 [+ o -] 0.2 R OC-CALB-TNBS-EDA R 7.6 [+ o -] 0.1 R OC-CALB-TNBS- R 6.1 [+ o -] 0.1 R EDA-TNBS Biocatalizador pH 7 pH 9 E (a) Enantio- E (a) preferencia OC-CALB 25.5 [+ o -] 0.2 R 8.9 [+ o -] 0.1 OC-CAL-EDA 35.6 [+ o -] 0.2 R 11.4 [+ o -] 0.1 OC-CALB-TNBS 22.2 [+ o -] 0.2 R 15.2 [+ o -] 0.1 OC-CALB-TNBS-EDA 27 [+ o -] 0.3 R 12.4 [+ o -] 0.1 OC-CALB-TNBS- 27.5 [+ o -] 0.15 R 12.2 [+ o -] 0.1 EDA-TNBS (a) El valor E se determino como la razon: Actividad frente a R-mandelato de metilo / Actividad frente a S-metil mandelato.

Modificacion Quimica en Fase Solida de Lipasa B de Candida antarctica para mejorar sus propiedades de actividad, estabilidad y enantioselectividad

reported that the highly polar phosphine oxide moiety of the chiral Michael catalyst interacts with the nitro group of Michael acceptor via dipole interactions mediated by water to produce high yield and enantio- and diastereoselectivity [14].

Proline based chiral ionic liquids for enantioselective Michael reaction

You, "Asymmetric Friedel-Crafts alkylation of indoles: the control of enantio- and regioselectivity," Synlett, vol.

Facile and promising method for Michael addition of indole and pyrrole to electron-deficient trans-[beta]-nitroolefins catalyzed by a hydrogen bond donor catalyst feist's acid and preliminary study of antimicrobial activity

His research interests centre on the design and development of catalytic carbon-carbon bond forming reactions for the enantio- and stereocontrolled synthesis of bioactive carbocycles and heterocycles.