-
1
-
-
0008591375
-
Síntese Estereosseletiva de 2-oxa biciclo [3.3.0] octanos funcionalizados
-
Barreiro, E.J., Garcia, V.L. Síntese Estereosseletiva de 2-oxa biciclo [3.3.0] octanos funcionalizados. An. Acad. Bras. Cienc. 57:417-428, 1985.
-
(1985)
An. Acad. Bras. Cienc.
, vol.57
, pp. 417-428
-
-
Barreiro, E.J.1
Garcia, V.L.2
-
2
-
-
0029759741
-
Enantiofacial selective reduction of 2-allyl-2-carboethoxy-cyclopentanone mediated by baker's yeast
-
Fraga, C.A.M., Barreiro, E.J. Enantiofacial selective reduction of 2-allyl-2-carboethoxy-cyclopentanone mediated by baker's yeast. Chirality 8: 305-310, 1996.
-
(1996)
Chirality
, vol.8
, pp. 305-310
-
-
Fraga, C.A.M.1
Barreiro, E.J.2
-
3
-
-
84982421074
-
Ûber die stereoselektivität der α-alkylierung von (1R.2S) (+)-cis-2-hydroxycyclohexancarbonsäureäthylester
-
Frater, G. Ûber die stereoselektivität der α-alkylierung von (1R.2S) (+)-cis-2-hydroxycyclohexancarbonsäureäthylester. Helv. Chim. Acta 63:1383-1390, 1980.
-
(1980)
Helv. Chim. Acta
, vol.63
, pp. 1383-1390
-
-
Frater, G.1
-
4
-
-
0026038391
-
Reduction by baker's yeast in benzene
-
Nakamura K, Kondo, S., Kawai, Y., Ohno, R. Reduction by baker's yeast in benzene. Tetrahedron Lett. 32:7075-7078, 1991.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 7075-7078
-
-
Nakamura, K.1
Kondo, S.2
Kawai, Y.3
Ohno, R.4
-
5
-
-
0027212868
-
The yeast mediated reduction of ethyl acetoacetate in petroleum ether
-
Jayasinghe, L.Y., Smallridge, A.J., Trewhella, M.A. The yeast mediated reduction of ethyl acetoacetate in petroleum ether. Tetrahedron Lett. 34:3949-3950, 1993.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 3949-3950
-
-
Jayasinghe, L.Y.1
Smallridge, A.J.2
Trewhella, M.A.3
-
6
-
-
0029964227
-
Baker's yeast reduction of β-keto esters in petrol
-
North, M. Baker's yeast reduction of β-keto esters in petrol. Tetrahedron Lett. 37:1699-1702, 1996.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 1699-1702
-
-
North, M.1
-
7
-
-
84985154137
-
Production of (+)-(S)-ethyl 3-hydroxybutyrate and (-)-(R)-ethyl-3-hydroxybutyrate by microbial reduction of ethyl acetoacetate; butyrate and (-)-(R)-ethyl-3-hydroxy-butyrate by microbial reduction of ethyl acetoacetate
-
Wipf, B., Kupfer, E., Bertazzi, R., Leuenberger, H.G.W. Production of (+)-(S)-ethyl 3-hydroxybutyrate and (-)-(R)-ethyl-3-hydroxybutyrate by microbial reduction of ethyl acetoacetate; butyrate and (-)-(R)-ethyl-3-hydroxy-butyrate by microbial reduction of ethyl acetoacetate. Helv. Chim. Acta 66:485-488, 1983.
-
(1983)
Helv. Chim. Acta
, vol.66
, pp. 485-488
-
-
Wipf, B.1
Kupfer, E.2
Bertazzi, R.3
Leuenberger, H.G.W.4
-
8
-
-
1842278908
-
-
note
-
Purchased from Otker Produtos Alimentícios Ltda, São Paulo, Brazil.
-
-
-
-
9
-
-
84913063444
-
Specification of the stereospecificity of some oxido-reductases by diamond lattice sections
-
Prelog, V. Specification of the stereospecificity of some oxido-reductases by diamond lattice sections. Pure Appl. Chem. 9:119-130, 1964.
-
(1964)
Pure Appl. Chem.
, vol.9
, pp. 119-130
-
-
Prelog, V.1
-
10
-
-
84985233025
-
Stereoisomeric flavor compounds. LVIII. The use of heptakis(2,3-di-O-methyl-6-O-t.butyldimethylsilyl)-β-cyclodextrin as a chiral stationary phase in flavor analysis
-
Dietrich, A., Maas, B., Messer, W., Bruche, G., Karl, V., Kaunzinger, A., Mosandl, A. Stereoisomeric flavor compounds. LVIII. The use of heptakis(2,3-di-O-methyl-6-O-t.butyldimethylsilyl)-β-cyclodextrin as a chiral stationary phase in flavor analysis. J. High Resol. Chromatogr. 15:590-593, 1992.
-
(1992)
J. High Resol. Chromatogr.
, vol.15
, pp. 590-593
-
-
Dietrich, A.1
Maas, B.2
Messer, W.3
Bruche, G.4
Karl, V.5
Kaunzinger, A.6
Mosandl, A.7
-
11
-
-
0342809470
-
Selective chemical modification of cyclomaltooligosaccharides via tert-butyldimethylsilylation
-
Takeo, K., Mitoh, H., Uemura, K. Selective chemical modification of cyclomaltooligosaccharides via tert-butyldimethylsilylation. Carbohydr. Res. 187:203-221, 1989.
-
(1989)
Carbohydr. Res.
, vol.187
, pp. 203-221
-
-
Takeo, K.1
Mitoh, H.2
Uemura, K.3
-
12
-
-
0028929525
-
Studies toward the diastereoselective reduction of 2-alkoxycarbonyl-2-allyl-cyclopentanone derivatives with boron hydrides
-
Fraga, C.A.M. Barreiro, E.J. Studies toward the diastereoselective reduction of 2-alkoxycarbonyl-2-allyl-cyclopentanone derivatives with boron hydrides. Synth. Commun. 25:1133-1144, 1995.
-
(1995)
Synth. Commun.
, vol.25
, pp. 1133-1144
-
-
Fraga, C.A.M.1
Barreiro, E.J.2
-
13
-
-
0025012727
-
Stereoselective synthesis of (2R,3S)-syn-2-allyl-3-hydroxy butanoate mediated by an enzymatic system from baker's yeast
-
Nakamura, K., Miyai, T., Kawai, Y., Nakajima, N., Ohno, A. Stereoselective synthesis of (2R,3S)-syn-2-allyl-3-hydroxy butanoate mediated by an enzymatic system from baker's yeast. Tetrahedron Lett. 31:1159-1160, 1990.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 1159-1160
-
-
Nakamura, K.1
Miyai, T.2
Kawai, Y.3
Nakajima, N.4
Ohno, A.5
-
14
-
-
0000414031
-
Stereochemical control of microbial reduction. XVII. A method for controlling the enantioselectivity of reductions with baker's yeast
-
Nakamura, K., Kawai, Y., Nakajima, N., Ohno, A. Stereochemical control of microbial reduction. XVII. A method for controlling the enantioselectivity of reductions with baker's yeast. J. Org. Chem. 56:4778-4783, 1991.
-
(1991)
J. Org. Chem.
, vol.56
, pp. 4778-4783
-
-
Nakamura, K.1
Kawai, Y.2
Nakajima, N.3
Ohno, A.4
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