-
1
-
-
0001067181
-
Enantioselective isomerization of allylamine to enamine: practical asymmetric synthesis of (-)-menthol by Rh-BINAP catalysts
-
Akutagawa S. Enantioselective isomerization of allylamine to enamine: practical asymmetric synthesis of (-)-menthol by Rh-BINAP catalysts. Top. Catal. 1997, 4:271-274.
-
(1997)
Top. Catal.
, vol.4
, pp. 271-274
-
-
Akutagawa, S.1
-
2
-
-
33745079610
-
Analysis of the reactions used for the preparation of drug candidate molecules
-
Carey J.S., Laffan D., Thomson C., Williams M.T. Analysis of the reactions used for the preparation of drug candidate molecules. Org. Biomol. Chem. 2006, 4:2337-2347.
-
(2006)
Org. Biomol. Chem.
, vol.4
, pp. 2337-2347
-
-
Carey, J.S.1
Laffan, D.2
Thomson, C.3
Williams, M.T.4
-
3
-
-
20644469267
-
Quantitative analyses of biochemical kinetic resolutions of enantiomers
-
Chen C.S., Fujimoto Y.F., Girdaukas G., Sih C.J. Quantitative analyses of biochemical kinetic resolutions of enantiomers. J. Am. Chem. Soc. 1982, 104:7294-7299.
-
(1982)
J. Am. Chem. Soc.
, vol.104
, pp. 7294-7299
-
-
Chen, C.S.1
Fujimoto, Y.F.2
Girdaukas, G.3
Sih, C.J.4
-
4
-
-
3342917497
-
Catalytic resolution of (RS)-HMPC acetate by immobilized cells of Acinetobacter sp. CGMCC 0789 in a medium with organic cosolvent
-
Chen Y., Xu J.H., Pan J., Xu Y., Shi J.B. Catalytic resolution of (RS)-HMPC acetate by immobilized cells of Acinetobacter sp. CGMCC 0789 in a medium with organic cosolvent. J. Mol. Catal. B: Enzyme 2004, 30:203-208.
-
(2004)
J. Mol. Catal. B: Enzyme
, vol.30
, pp. 203-208
-
-
Chen, Y.1
Xu, J.H.2
Pan, J.3
Xu, Y.4
Shi, J.B.5
-
6
-
-
50349091008
-
Aroma chemical profile: menthol
-
Clark G.S. Aroma chemical profile: menthol. Perfumer & Flavorist 2007, 32:38-47.
-
(2007)
Perfumer & Flavorist
, vol.32
, pp. 38-47
-
-
Clark, G.S.1
-
7
-
-
0035424201
-
Using proteins in their natural environment: potential and limitations of microbial whole-cell hydroxylations in applied biocatalysis
-
Duetz W.A., Beilen J.B., Witholt B. Using proteins in their natural environment: potential and limitations of microbial whole-cell hydroxylations in applied biocatalysis. Curr. Opin. Biotechnol. 2001, 12:419-425.
-
(2001)
Curr. Opin. Biotechnol.
, vol.12
, pp. 419-425
-
-
Duetz, W.A.1
Beilen, J.B.2
Witholt, B.3
-
10
-
-
0030731108
-
The complete genome sequence of the gram-positive bacterium Bacillus subtilis
-
Kunst F., Ogasawara N., et al. The complete genome sequence of the gram-positive bacterium Bacillus subtilis. Nature 1997, 390:249-256.
-
(1997)
Nature
, vol.390
, pp. 249-256
-
-
Kunst, F.1
Ogasawara, N.2
-
12
-
-
0042497321
-
Asymmetric catalysis: science and opportunities
-
Noyori R. Asymmetric catalysis: science and opportunities. Adv. Synth. Catal. 2003, 345:15-32.
-
(2003)
Adv. Synth. Catal.
, vol.345
, pp. 15-32
-
-
Noyori, R.1
-
13
-
-
0019419612
-
Stereoselective hydrolysis of dl-menthyl succinate by gel-entrapped Rhodotorula minuta var. texensis cells in organic solvent
-
Omata T., Iwamoto N., Kimura T., Tanaka A., Fukui S. Stereoselective hydrolysis of dl-menthyl succinate by gel-entrapped Rhodotorula minuta var. texensis cells in organic solvent. Eur. J. Appl. Microbiol. Biotechnol. 1981, 11:199-204.
-
(1981)
Eur. J. Appl. Microbiol. Biotechnol.
, vol.11
, pp. 199-204
-
-
Omata, T.1
Iwamoto, N.2
Kimura, T.3
Tanaka, A.4
Fukui, S.5
-
14
-
-
0036525716
-
Lipases as practical biocatalysts
-
Reetz M.T. Lipases as practical biocatalysts. Curr. Opin. Chem. Biol. 2002, 6:, 145-150.
-
(2002)
Curr. Opin. Chem. Biol.
, vol.6
, pp. 145-150
-
-
Reetz, M.T.1
-
15
-
-
0035843170
-
Industrial biocatalysis today and tomorrow
-
Schmid A., Dordick J.S., Hauer B., Kiener A., Wubbolts M., Witholt B. Industrial biocatalysis today and tomorrow. Nature 2001, 409:258-268.
-
(2001)
Nature
, vol.409
, pp. 258-268
-
-
Schmid, A.1
Dordick, J.S.2
Hauer, B.3
Kiener, A.4
Wubbolts, M.5
Witholt, B.6
-
16
-
-
34547209337
-
Enzyme immobilization: the quest for optimum performance
-
Sheldon R.A. Enzyme immobilization: the quest for optimum performance. Adv. Synth. Catal. 2007, 349:1289-1307.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1289-1307
-
-
Sheldon, R.A.1
-
17
-
-
2342559067
-
Highly selective synthesis of menthols from citral in a one-step process
-
Trasarti A.F., Marchi A.J., Apesteguia C.R. Highly selective synthesis of menthols from citral in a one-step process. J. Catal. 2004, 224:484-488.
-
(2004)
J. Catal.
, vol.224
, pp. 484-488
-
-
Trasarti, A.F.1
Marchi, A.J.2
Apesteguia, C.R.3
-
18
-
-
0031023666
-
'Interfacial activation' of lipases: facts and artifacts
-
Verger R. 'Interfacial activation' of lipases: facts and artifacts. Trends Biotechnol. 1997, 15:32-38.
-
(1997)
Trends Biotechnol.
, vol.15
, pp. 32-38
-
-
Verger, R.1
-
19
-
-
0142142207
-
Enantioselective hydrolysis of dl-menthyl benzoate to l-(-)-menthol by recombinant Candida rugosa lipase LIP1
-
Vorlova S., Bronscheuer U.T., Gatfield I., Hilmer J.M., Bertram H.J., Schmid R.D. Enantioselective hydrolysis of dl-menthyl benzoate to l-(-)-menthol by recombinant Candida rugosa lipase LIP1. Adv. Synth. Catal. 2002, 344:1152-1155.
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 1152-1155
-
-
Vorlova, S.1
Bronscheuer, U.T.2
Gatfield, I.3
Hilmer, J.M.4
Bertram, H.J.5
Schmid, R.D.6
-
21
-
-
34547207256
-
New developments in biocatalysis
-
Wong C.H. New developments in biocatalysis. Adv. Synth. Catal. 2007, 349:1287.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 1287
-
-
Wong, C.H.1
-
22
-
-
0343703438
-
Lipase-catalyzed stereoselective esterification of DL-menthol in organic solvents using acid anhydrides as acylating agents
-
Wu W.H., Akoh C.C., Phillips R.S. Lipase-catalyzed stereoselective esterification of DL-menthol in organic solvents using acid anhydrides as acylating agents. Enzyme Microb. Technol. 1996, 18:536-539.
-
(1996)
Enzyme Microb. Technol.
, vol.18
, pp. 536-539
-
-
Wu, W.H.1
Akoh, C.C.2
Phillips, R.S.3
-
23
-
-
0029125374
-
Efficient kinetic resolution of dl-menthol by lipase-catalyzed enantioselective esterification with acid anhydride in fed-batch reactor
-
Xu J.H., Kawamoto T., Tanaka A. Efficient kinetic resolution of dl-menthol by lipase-catalyzed enantioselective esterification with acid anhydride in fed-batch reactor. Appl. Microbiol. Biotechnol. 1995, 43:402-407.
-
(1995)
Appl. Microbiol. Biotechnol.
, vol.43
, pp. 402-407
-
-
Xu, J.H.1
Kawamoto, T.2
Tanaka, A.3
-
24
-
-
34447270575
-
Highly enantioselective hydrolysis of dl-menthyl acetate to l-menthol by whole-cell lipase from Burkholderia cepacia ATCC 25416
-
Yu L.J., Xu Y., Wang X.Q., Yu X.W. Highly enantioselective hydrolysis of dl-menthyl acetate to l-menthol by whole-cell lipase from Burkholderia cepacia ATCC 25416. J. Mol. Catal. B: Enzyme 2007, 47:149-154.
-
(2007)
J. Mol. Catal. B: Enzyme
, vol.47
, pp. 149-154
-
-
Yu, L.J.1
Xu, Y.2
Wang, X.Q.3
Yu, X.W.4
-
25
-
-
42749092984
-
Biochemical properties and potential applications of an organic solvent tolerant lipase isolated from Serratia marcescens ECU1010
-
Zhao L.L., Xu J.H., Zhao J., Pan J., Wang Z.L. Biochemical properties and potential applications of an organic solvent tolerant lipase isolated from Serratia marcescens ECU1010. Process Biochem. 2008, 43:626-633.
-
(2008)
Process Biochem.
, vol.43
, pp. 626-633
-
-
Zhao, L.L.1
Xu, J.H.2
Zhao, J.3
Pan, J.4
Wang, Z.L.5
-
26
-
-
60849119553
-
Enzymatic production of l-menthol by a high substrate concentration tolerable esterase from newly isolated Bacillus subtilis ECU0554
-
Zheng G.W., Yu H.L., Zhang J.D., Xu J.H. Enzymatic production of l-menthol by a high substrate concentration tolerable esterase from newly isolated Bacillus subtilis ECU0554. Adv. Synth. Catal. 2009, 351:405-414.
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 405-414
-
-
Zheng, G.W.1
Yu, H.L.2
Zhang, J.D.3
Xu, J.H.4
|