-
1
-
-
0042074583
-
Silicon chemistry as a novel source of chemical diversity in drug design
-
Bains, W., Tacke, R., "Silicon chemistry as a novel source of chemical diversity in drug design", Curr. Opin. Drug Di. De., 8, 526-543 (2003).
-
(2003)
Curr. Opin. Drug Di. De.
, vol.8
, pp. 526-543
-
-
Bains, W.1
Tacke, R.2
-
2
-
-
0035888133
-
Immobilized baker's yeast reduction of ketones in an ionic liquid, [bmim] PF6 and water mix
-
Howarth, J., James, P., Dai, J.F., "Immobilized baker's yeast reduction of ketones in an ionic liquid, [bmim] PF6 and water mix", Tetrahedron Lett., 42, 7517-7519 (2001).
-
(2001)
Tetrahedron Lett.
, vol.42
, pp. 7517-7519
-
-
Howarth, J.1
James, P.2
Dai, J.F.3
-
3
-
-
0032963235
-
A novel stereoselective reaction cascade leading from α-silylated allylic alcohols to aldol-type products
-
Fassler, J., Enev, V., Bienz, S., "A novel stereoselective reaction cascade leading from α-silylated allylic alcohols to aldol-type products", Helv. Chim. Acta., 82, 561-587 (1999).
-
(1999)
Helv. Chim. Acta.
, vol.82
, pp. 561-587
-
-
Fassler, J.1
Enev, V.2
Bienz, S.3
-
4
-
-
0035931443
-
Biotransformation of organosilicon compounds: Enantioselective reduction of acyl silanes by means of baker's yeast
-
Zani, P., "Biotransformation of organosilicon compounds: Enantioselective reduction of acyl silanes by means of baker's yeast", J. Mol. Catal. B Enzym., 11, 279-285 (2001).
-
(2001)
J. Mol. Catal. B Enzym.
, vol.11
, pp. 279-285
-
-
Zani, P.1
-
5
-
-
0026472165
-
Kinetic resolution of organosilicon compounds by stereoselective dehydrogenation with horse liver alcohol dehydrogenase
-
Fukui, T., Zong, M.H., Kawamoto, T., Tanaka, A., "Kinetic resolution of organosilicon compounds by stereoselective dehydrogenation with horse liver alcohol dehydrogenase", Appl. Microbiol. Biotechnol., 38, 209-213 (1992).
-
(1992)
Appl. Microbiol. Biotechnol.
, vol.38
, pp. 209-213
-
-
Fukui, T.1
Zong, M.H.2
Kawamoto, T.3
Tanaka, A.4
-
6
-
-
0027404437
-
Efficient kinetic resolution of organosilicon compounds by stereoselective esterification with hydrolases in organic solvent
-
Uejima, A., Fukui, T., Fukusaki, E., Omata, T., Kawamoto, T., Sonomoto, K., Tanaka, A., "Efficient kinetic resolution of organosilicon compounds by stereoselective esterification with hydrolases in organic solvent", Appl. Microbiol. Biotechnol., 38, 482-486 (1993).
-
(1993)
Appl. Microbiol. Biotechnol.
, vol.38
, pp. 482-486
-
-
Uejima, A.1
Fukui, T.2
Fukusaki, E.3
Omata, T.4
Kawamoto, T.5
Sonomoto, K.6
Tanaka, A.7
-
7
-
-
0000024647
-
The asymmetric hydroboration of simple alkenylsilanes: Chiral α-silylalkylboranes and alcohols
-
Soderquist, J.A., Hwang-Lee, S.J., "The asymmetric hydroboration of simple alkenylsilanes: Chiral α-silylalkylboranes and alcohols", Tetrahedron, 44, 4033-4042 (1988).
-
(1988)
Tetrahedron
, vol.44
, pp. 4033-4042
-
-
Soderquist, J.A.1
Hwang-Lee, S.J.2
-
8
-
-
0025278992
-
Essentially homochiral 1-silyl alcohols from the reduction of aliphatic acylsilanes with chlorodiisopinocampheylborane
-
Soderquist, J.A., Anderson, C.L., Miranda, E.I., Rivera, I., "Essentially homochiral 1-silyl alcohols from the reduction of aliphatic acylsilanes with chlorodiisopinocampheylborane", Tetrahedron Lett., 31, 4677-4680 (1990).
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 4677-4680
-
-
Soderquist, J.A.1
Anderson, C.L.2
Miranda, E.I.3
Rivera, I.4
-
9
-
-
17444446443
-
Biocatalytic synthesis of (-)-1-trimethylsilylethanol by asymmetric reduction of acetyltrimethylsilane with a new isolate Rhodotorula sp. AS2.2241
-
Luo, D.H., Zong, M.H., Xu, J.H., "Biocatalytic synthesis of (-)-1-trimethylsilylethanol by asymmetric reduction of acetyltrimethylsilane with a new isolate Rhodotorula sp. AS2.2241", J. Mol. Catal. B Enzym., 24-25, 83-88 (2003).
-
(2003)
J. Mol. Catal. B Enzym.
, vol.24-25
, pp. 83-88
-
-
Luo, D.H.1
Zong, M.H.2
Xu, J.H.3
-
10
-
-
0029125374
-
Efficient kinetic resolution of d-menthol by lipase-catalyzed enantioselective esteriflcation with acid anhydride in fed-batch reactor
-
Xu, J.H., Kawamoto, T., Tanaka, A., "Efficient kinetic resolution of d-menthol by lipase-catalyzed enantioselective esteriflcation with acid anhydride in fed-batch reactor", Appl. Microbiol. Biotechnol., 43, 402-407 (1995).
-
(1995)
Appl. Microbiol. Biotechnol.
, vol.43
, pp. 402-407
-
-
Xu, J.H.1
Kawamoto, T.2
Tanaka, A.3
-
11
-
-
0026863988
-
Temperature effects on stereochemistry of enzymatic reaction
-
Phillips, R.S., "Temperature effects on stereochemistry of enzymatic reaction", Enzyme Microb. Technol., 14, 417-419 (1992).
-
(1992)
Enzyme Microb. Technol.
, vol.14
, pp. 417-419
-
-
Phillips, R.S.1
-
12
-
-
0027990305
-
High enantioselective esterincation of 2-arylpropionic acids catalyzed by immobilized lipase from Candida antarctica: A mechanistic approach
-
Arroyo, M., Sinisterra, J.V., "High enantioselective esterincation of 2-arylpropionic acids catalyzed by immobilized lipase from Candida antarctica: A mechanistic approach", J. Org. Chem., 59, 4410 - 4417 (1994).
-
(1994)
J. Org. Chem.
, vol.59
, pp. 4410-4417
-
-
Arroyo, M.1
Sinisterra, J.V.2
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