-
12
-
-
0001716385
-
-
Aldehyde and ketone reviews:
-
Aldehyde and ketone reviews:. MacLeod R., Prosser H., Fikentscher L., Lanyi J., and Mosher H.S. Biochemistry 3 (1964) 838
-
(1964)
Biochemistry
, vol.3
, pp. 838
-
-
MacLeod, R.1
Prosser, H.2
Fikentscher, L.3
Lanyi, J.4
Mosher, H.S.5
-
16
-
-
0036037363
-
-
Kayser M.M., Yang Y., Mihovilovic M.D., Feicht A., and Rochon F.D. Can. J. Chem. 80 (2002) 796
-
(2002)
Can. J. Chem.
, vol.80
, pp. 796
-
-
Kayser, M.M.1
Yang, Y.2
Mihovilovic, M.D.3
Feicht, A.4
Rochon, F.D.5
-
22
-
-
0034343831
-
-
Pavlov V.A., Starodubtseva E.V., Vinogradov M.G., Ferapontov V.A., Malyshev O.R., and Heise G.L. Russ. Chem. Bull. 49 (2000) 728
-
(2000)
Russ. Chem. Bull.
, vol.49
, pp. 728
-
-
Pavlov, V.A.1
Starodubtseva, E.V.2
Vinogradov, M.G.3
Ferapontov, V.A.4
Malyshev, O.R.5
Heise, G.L.6
-
26
-
-
39849109293
-
-
Davies G.H., Gartenmann C.C., Leaver J., Roberts S.M., and Turner M.K. Tetrahedron Lett. 27 (1986) 1093
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 1093
-
-
Davies, G.H.1
Gartenmann, C.C.2
Leaver, J.3
Roberts, S.M.4
Turner, M.K.5
-
28
-
-
0005768892
-
-
Hudlicky T., Tsunoda T., Gadamasetti G., Murry J., and Keck G. J. Org. Chem. 56 (1991) 3619
-
(1991)
J. Org. Chem.
, vol.56
, pp. 3619
-
-
Hudlicky, T.1
Tsunoda, T.2
Gadamasetti, G.3
Murry, J.4
Keck, G.5
-
29
-
-
41449087642
-
-
The surprising absence of such investigations until 1991 was most likely due to the lack of yeast reductions of esters other than those derived from methyl, ethyl, propyl, butyl and benzyl alcohols, the most commonly used substrates.
-
The surprising absence of such investigations until 1991 was most likely due to the lack of yeast reductions of esters other than those derived from methyl, ethyl, propyl, butyl and benzyl alcohols, the most commonly used substrates.
-
-
-
-
31
-
-
41449110218
-
-
Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. (in part) Synlett 1990, 433.
-
Hudlicky, T.; Seoane, G.; Price, J. D.; Gadamasetti, K. (in part) Synlett 1990, 433.
-
-
-
-
34
-
-
84988058551
-
-
Enders D., Kipphardt H., Gerdes P., Brena-Valle L.J., and Bhushan V. Bull. Soc. Chim. Belg. 97 (1988) 691
-
(1988)
Bull. Soc. Chim. Belg.
, vol.97
, pp. 691
-
-
Enders, D.1
Kipphardt, H.2
Gerdes, P.3
Brena-Valle, L.J.4
Bhushan, V.5
-
35
-
-
33845648990
-
-
Albertshofer K., Thayumanavan R., Utsumi N., Tanaka F., and Barbas III C.F. Tetrahedron Lett. 48 (2007) 693
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 693
-
-
Albertshofer, K.1
Thayumanavan, R.2
Utsumi, N.3
Tanaka, F.4
Barbas III, C.F.5
-
37
-
-
33750329521
-
-
Amat M., Bassas O., Llor N., Cantó M., Pérez M., Molins E., and Bosch J. Chem. Eur. J. 12 (2006) 7872
-
(2006)
Chem. Eur. J.
, vol.12
, pp. 7872
-
-
Amat, M.1
Bassas, O.2
Llor, N.3
Cantó, M.4
Pérez, M.5
Molins, E.6
Bosch, J.7
-
38
-
-
41449086316
-
-
We want to thank Núria Llor and Professor Joan Bosch for helpful advice for the synthesis of the enantiomerically enriched standard 26. In repetition of this work, we were unable to obtain the enantiomeric excess of 99% reported (Ref. 13).
-
We want to thank Núria Llor and Professor Joan Bosch for helpful advice for the synthesis of the enantiomerically enriched standard 26. In repetition of this work, we were unable to obtain the enantiomeric excess of 99% reported (Ref. 13).
-
-
-
-
39
-
-
41449098366
-
-
No resolution with yeast reduction was observed for 2-phenyl-3,4-dihydro-2H-quinoline as substrate{A figure is presented}.
-
No resolution with yeast reduction was observed for 2-phenyl-3,4-dihydro-2H-quinoline as substrate{A figure is presented}.
-
-
-
-
40
-
-
41449110592
-
-
K1 V1116, EC 1118, CY 3079, and BA 11 are commercial wine yeast strains available from Scott Laboratories.
-
K1 V1116, EC 1118, CY 3079, and BA 11 are commercial wine yeast strains available from Scott Laboratories.
-
-
-
-
41
-
-
33845282793
-
-
Noyori R., Ohkuma T., Kitamura M., Takaya H., Sayo N., Kumobayashi H., and Akutagawa S. J. Am. Chem. Soc. 109 (1987) 5856
-
(1987)
J. Am. Chem. Soc.
, vol.109
, pp. 5856
-
-
Noyori, R.1
Ohkuma, T.2
Kitamura, M.3
Takaya, H.4
Sayo, N.5
Kumobayashi, H.6
Akutagawa, S.7
|