-
1
-
-
0032829456
-
Commercial Scale Biocatalysis: Myths and Realities
-
Rozzell, J.D. Commercial Scale Biocatalysis: Myths and Realities. Bioorg. Med. Chem., 1999, 7, 2253-2261.
-
(1999)
Bioorg. Med. Chem
, vol.7
, pp. 2253-2261
-
-
Rozzell, J.D.1
-
2
-
-
0001389723
-
Biotransformations-A useful tool in organic chemistry
-
Leunberger, H.G.W. Biotransformations-A useful tool in organic chemistry. Pure Appl. Chem., 1990, 62(4), 753-768.
-
(1990)
Pure Appl. Chem
, vol.62
, Issue.4
, pp. 753-768
-
-
Leunberger, H.G.W.1
-
3
-
-
0034606771
-
The role of catalysis in the design, development, and implementation of green chemistry
-
Anastas, P.T.; Bartlett, L.B.; Kirchoff, M. M; Williamson, T.C. The role of catalysis in the design, development, and implementation of green chemistry. Catal. Today, 2000, 55, 11-22.
-
(2000)
Catal. Today
, vol.55
, pp. 11-22
-
-
Anastas, P.T.1
Bartlett, L.B.2
Kirchoff, M.M.3
Williamson, T.C.4
-
4
-
-
0033556602
-
Biocatalytic transformation of racemates into chiral building blocks in 100% chemical yield and 100% enantiomeric excess
-
Strauss, U.T.; Felfer, U.; Faber, K. Biocatalytic transformation of racemates into chiral building blocks in 100% chemical yield and 100% enantiomeric excess. Tetrahedron-Asymmetr., 1999, 10, 107-117.
-
(1999)
Tetrahedron-Asymmetr
, vol.10
, pp. 107-117
-
-
Strauss, U.T.1
Felfer, U.2
Faber, K.3
-
5
-
-
22244486966
-
Resolution of enantiomers by non-conventional methods
-
Fogassy, E.; Nogradi, M.; Palovies, E.; Schindler, J. Resolution of enantiomers by non-conventional methods. Synthesis, 2005, 10, 1556-1568.
-
(2005)
Synthesis
, vol.10
, pp. 1556-1568
-
-
Fogassy, E.1
Nogradi, M.2
Palovies, E.3
Schindler, J.4
-
6
-
-
0242438894
-
20 years of biotransformations
-
Show, N.M.; Robins, K.T.; Kiener, A. 20 years of biotransformations. Adv. Synth. Catal., 2003, 345 (4), 425-435.
-
(2003)
Adv. Synth. Catal
, vol.345
, Issue.4
, pp. 425-435
-
-
Show, N.M.1
Robins, K.T.2
Kiener, A.3
-
7
-
-
2942560845
-
Strain improvement for fermentation and biocatalysis processes by genetic engineering technology
-
Chiang, S-J. Strain improvement for fermentation and biocatalysis processes by genetic engineering technology. J. Ind. Microbiol. Biotechnol., 2004, 31, 99-108.
-
(2004)
J. Ind. Microbiol. Biotechnol
, vol.31
, pp. 99-108
-
-
Chiang, S-J.1
-
8
-
-
0027426916
-
Whole cell biocatalysis in nonconventional media
-
Nikolova, P.; Ward, O.P. Whole cell biocatalysis in nonconventional media. J. Ind. Microbiol., 1993, 12, 76-86.
-
(1993)
J. Ind. Microbiol
, vol.12
, pp. 76-86
-
-
Nikolova, P.1
Ward, O.P.2
-
9
-
-
85197362362
-
-
In:, Górecki, H.; Dobrzański, Z.; Kafarski, P., Ed.; Czech_Pol Trade: Prague
-
Zymańczyk-Duda, E.; Brzezińska-Rodak, M.; Niewiadomska, A. In: Chemistry and Agriculture; Górecki, H.; Dobrzański, Z.; Kafarski, P., Ed.; Czech_Pol Trade: Prague, 2003; Vol.4, pp.590-593.
-
(2003)
Chemistry and Agriculture
, vol.4
, pp. 590-593
-
-
Zymańczyk-Duda, E.1
Brzezińska-Rodak, M.2
Niewiadomska, A.3
-
10
-
-
0030661956
-
Production of (2S,3S)-2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, a key intermediate for ditiazem synthesis by bakers' yeast-mediated reduction
-
Kometani, T.; Sakai, Y.; Matsumae, H.; Shibatani, T.; Matsuno, R. Production of (2S,3S)-2,3-dihydro-3-hydroxy-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, a key intermediate for ditiazem synthesis by bakers' yeast-mediated reduction. J. Ferment. Bioeng., 1997, 84, 195-199.
-
(1997)
J. Ferment. Bioeng
, vol.84
, pp. 195-199
-
-
Kometani, T.1
Sakai, Y.2
Matsumae, H.3
Shibatani, T.4
Matsuno, R.5
-
11
-
-
0032886388
-
Baker's yeast-mediated reductions of α-keto esters and an α-keto-β-lactam. Two routes to the paclitaxel side chain
-
Kayser, M.M.; Mihovilovic, M.D.; Kearns, J.; Feicht, A.; Stewart, J.D. Baker's yeast-mediated reductions of α-keto esters and an α-keto-β-lactam. Two routes to the paclitaxel side chain. J. Org. Chem., 1999, 64, 6603-6608.
-
(1999)
J. Org. Chem
, vol.64
, pp. 6603-6608
-
-
Kayser, M.M.1
Mihovilovic, M.D.2
Kearns, J.3
Feicht, A.4
Stewart, J.D.5
-
12
-
-
0000414031
-
Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast
-
Nakamura, K.; Kawai, Y.; Nakajima, N.; Ohno, A. Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast. J. Org. Chem., 1991, 56, 4778-4783.
-
(1991)
J. Org. Chem
, vol.56
, pp. 4778-4783
-
-
Nakamura, K.1
Kawai, Y.2
Nakajima, N.3
Ohno, A.4
-
13
-
-
0029964599
-
Microbial Synthesis of (+)-(3R)-Ethyl 3-hydroxy-3-(3,4-dimethoxyphenyl)propionate
-
Bardot, V.; Besse, P.; Gelas-Miahle, Y.; Remuson, R.; Veschambre, H. Microbial Synthesis of (+)-(3R)-Ethyl 3-hydroxy-3-(3,4-dimethoxyphenyl)propionate. Tetrahedron-Asymmetr., 1996, 7, 1077-1088.
-
(1996)
Tetrahedron-Asymmetr
, vol.7
, pp. 1077-1088
-
-
Bardot, V.1
Besse, P.2
Gelas-Miahle, Y.3
Remuson, R.4
Veschambre, H.5
-
14
-
-
0000714772
-
Enzymes in organic synthesis
-
Jones, J.B. Enzymes in organic synthesis. Tetrahedron, 1986, 42, 3351-3400.
-
(1986)
Tetrahedron
, vol.42
, pp. 3351-3400
-
-
Jones, J.B.1
-
15
-
-
0036669430
-
The use of enzymes in the chemical industry in Europe
-
Schmidt, A.; Hollmann, F.; Park, J.B.; Buhler, B. The use of enzymes in the chemical industry in Europe. Curr. Opinion Biotechnol., 2003, 13, 359-366.
-
(2003)
Curr. Opinion Biotechnol
, vol.13
, pp. 359-366
-
-
Schmidt, A.1
Hollmann, F.2
Park, J.B.3
Buhler, B.4
-
16
-
-
1842578074
-
Industrial methods for the production of optically active intermediates
-
Breuer, M.; Ditrich, K.; Habicher, T.; Hauer, B.; Kebeler, M.; Sturmer, R.; Zielinski, T. Industrial methods for the production of optically active intermediates. Angew. Chem. Int. Ed. Engi., 2004, 43, 788-824.
-
(2004)
Angew. Chem. Int. Ed. Engi
, vol.43
, pp. 788-824
-
-
Breuer, M.1
Ditrich, K.2
Habicher, T.3
Hauer, B.4
Kebeler, M.5
Sturmer, R.6
Zielinski, T.7
-
17
-
-
76449102390
-
Biological activity of aminophosphonic acids and their short peptides
-
Lejczak, B.; Kafarski, P. Biological activity of aminophosphonic acids and their short peptides. Top Heterocycl. Chem., 2009, 20, 31-63.
-
(2009)
Top Heterocycl. Chem
, vol.20
, pp. 31-63
-
-
Lejczak, B.1
Kafarski, P.2
-
18
-
-
77952475238
-
Isoprenoid biosynthesis via the methylerythritol phosphate pathway: Structural variations around phosphonate anchor and spacer of fosmidomycin, a potent inhibitor of deoxyxylulose phosphate reductoisomerase
-
Zingle, C.; Kuntz, L.; Trisch, D.; Grosdemange-Billiard, C.; Rohmer, M. Isoprenoid biosynthesis via the methylerythritol phosphate pathway: structural variations around phosphonate anchor and spacer of fosmidomycin, a potent inhibitor of deoxyxylulose phosphate reductoisomerase. J. Org. Chem., 2010, 75, 3203-3207.
-
(2010)
J. Org. Chem
, vol.75
, pp. 3203-3207
-
-
Zingle, C.1
Kuntz, L.2
Trisch, D.3
Grosdemange-Billiard, C.4
Rohmer, M.5
-
19
-
-
74849128053
-
Synthesis and biological activity of O, O-dimethyl-2,6-pyridinyl diformyloxy alkyl phosphonates
-
Wang, T.; Lei, D.Y.; Huang, Y.; Ao, L.H. Synthesis and biological activity of O, O-dimethyl-2,6-pyridinyl diformyloxy alkyl phosphonates. Phosphorus Sulfur, 2009, 184, 2777-2785.
-
(2009)
Phosphorus Sulfur
, vol.184
, pp. 2777-2785
-
-
Wang, T.1
Lei, D.Y.2
Huang, Y.3
Ao, L.H.4
-
20
-
-
66349127137
-
Stereoselective synthesis and biological activities of diethyl (E)-{[4-cyano-5-[(disubstitutedamino)methylene]amino]-3-(methylthio)-1H-pyrazol-1-yl]substituited phenylmethyl}phosphonates
-
Xiao, L.X.; Shi, D.Q. Stereoselective synthesis and biological activities of diethyl (E)-{[4-cyano-5-[(disubstitutedamino)methylene]amino]-3-(methylthio)-1H-pyrazol-1-yl]substituited phenylmethyl}phosphonates. J. Heterocyclic Chem., 2009, 46, 555-559.
-
(2009)
J. Heterocyclic Chem
, vol.46
, pp. 555-559
-
-
Xiao, L.X.1
Shi, D.Q.2
-
21
-
-
0000627987
-
Isolation of 2-aminoethanephosphonic acid from rumen protozoa
-
Horiguchi, M.; Kandatsu, M. Isolation of 2-aminoethanephosphonic acid from rumen protozoa. Nature, 1959, 184, 901-902.
-
(1959)
Nature
, vol.184
, pp. 901-902
-
-
Horiguchi, M.1
Kandatsu, M.2
-
22
-
-
33646579351
-
Inhibition of glutamine synthetase by phosphonic analogues of glutamic acid
-
Mastalerz, P. Inhibition of glutamine synthetase by phosphonic analogues of glutamic acid. Arch. Immunol. Ther. Exp. 1959, 7, 201-210.
-
(1959)
Arch. Immunol. Ther. Exp
, vol.7
, pp. 201-210
-
-
Mastalerz, P.1
-
23
-
-
27944467415
-
Computer-aided analysis and design of phosphonic and phosphinic enzyme inhibitors as potential drugs and agrochemicals
-
Berlicki, L.; Kafarski, P. Computer-aided analysis and design of phosphonic and phosphinic enzyme inhibitors as potential drugs and agrochemicals. Curr. Org. Chem., 2005, 9, 1829-1850.
-
(2005)
Curr. Org. Chem
, vol.9
, pp. 1829-1850
-
-
Berlicki, L.1
Kafarski, P.2
-
24
-
-
26444495633
-
Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase
-
Berlicki, L.; Grabowiecka, A.; Forlani, G.; Kafarski, P. Design, synthesis, and activity of analogues of phosphinothricin as inhibitors of glutamine synthetase. J. Med. Chem., 2006, 48, 6340-6349.
-
(2006)
J. Med. Chem
, vol.48
, pp. 6340-6349
-
-
Berlicki, L.1
Grabowiecka, A.2
Forlani, G.3
Kafarski, P.4
-
25
-
-
2342618859
-
Development of irreversible diphenyl phosphonate inhibitors for urokinase plasminogen activator
-
Joossens, J.; Van Der Veken, P.; Lambier, A.M.; Augustyns, K.; Haemers, A. Development of irreversible diphenyl phosphonate inhibitors for urokinase plasminogen activator. J. Med. Chem., 2004, 47(10), 2411-2413.
-
(2004)
J. Med. Chem
, vol.47
, Issue.10
, pp. 2411-2413
-
-
Joossens, J.1
van der Veken, P.2
Lambier, A.M.3
Augustyns, K.4
Haemers, A.5
-
26
-
-
0037073950
-
Synthesis and antituberculosis activity of Cphosphonate analogues of decaprenolphosphoarabinose, a key intermediate in the biosynthesis of mycobacterial arabinogalactan and lipoarabinomannan
-
Centrone, C.A.; Lowary, T.L. Synthesis and antituberculosis activity of Cphosphonate analogues of decaprenolphosphoarabinose, a key intermediate in the biosynthesis of mycobacterial arabinogalactan and lipoarabinomannan. J. Org. Chem., 2002, 67(25), 8862-8870.
-
(2002)
J. Org. Chem
, vol.67
, Issue.25
, pp. 8862-8870
-
-
Centrone, C.A.1
Lowary, T.L.2
-
27
-
-
0141988884
-
Inhibition of dog and human gastric lipases by enantiomeric phosphonate inhibitors: A structure-activity study
-
Miled, N.; Russel, A.; Bussetta, C.; Berti-Dupuis, L.; Riviere, M.; Buono, G.; Verger, R.; Cambillau, C.; Canaan, S. Inhibition of dog and human gastric lipases by enantiomeric phosphonate inhibitors: a structure-activity study. Biochemistry, 2003, 42(40), 11587-11593.
-
(2003)
Biochemistry
, vol.42
, Issue.40
, pp. 11587-11593
-
-
Miled, N.1
Russel, A.2
Bussetta, C.3
Berti-Dupuis, L.4
Riviere, M.5
Buono, G.6
Verger, R.7
Cambillau, C.8
Canaan, S.9
-
28
-
-
0037077789
-
Synthesis and biological evaluation of (R)-and (S)-2-(phosphonomethyl)pentanedioic acids as inhibitors of glutamate carboxypeptidase II
-
Vithrana, D.; France, J.E.; Scarpetti, D.; Bonneville, G.W.; Majer, P.; Tsukamoto, T. Synthesis and biological evaluation of (R)-and (S)-2-(phosphonomethyl)pentanedioic acids as inhibitors of glutamate carboxypeptidase II. Tetrahedron-Asymmetr., 2002, 13, 1609-1614.
-
(2002)
Tetrahedron-Asymmetr
, vol.13
, pp. 1609-1614
-
-
Vithrana, D.1
France, J.E.2
Scarpetti, D.3
Bonneville, G.W.4
Majer, P.5
Tsukamoto, T.6
-
29
-
-
4744357516
-
Inhibition of isoprene biosynthesis pathway enzymes by phosphonates, bisphosphonates, and diphosphates
-
Cheng, F.; Oldfield, E. Inhibition of isoprene biosynthesis pathway enzymes by phosphonates, bisphosphonates, and diphosphates. J. Med. Chem., 2004, 47(21), 5149-5158.
-
(2004)
J. Med. Chem
, vol.47
, Issue.21
, pp. 5149-5158
-
-
Cheng, F.1
Oldfield, E.2
-
30
-
-
33846845012
-
Design, synthesis, and evaluation of gamma-phosphono diester analogues of glutamate as highly potent inhibitors and active site probes of gamma-glutamyl transpeptidase
-
Han, L.; Hiratake, J.; Kamiyama, A.; Sakata, K. Design, synthesis, and evaluation of gamma-phosphono diester analogues of glutamate as highly potent inhibitors and active site probes of gamma-glutamyl transpeptidase. Biochemistry, 2007, 46(5), 1432-1447.
-
(2007)
Biochemistry
, vol.46
, Issue.5
, pp. 1432-1447
-
-
Han, L.1
Hiratake, J.2
Kamiyama, A.3
Sakata, K.4
-
31
-
-
79953284806
-
N5-phosphonoacetyl-L-ornithine (PALO): A convenient synthesis and investigation of influence on regulation of amino acid biosynthetic genes in Saccharomyces cerevisiae
-
Jonson, B.; Steadman, R.; Patefield, K.D.; Bunker, J.J.; Atkin, A.L.; Dussault, P. N5-phosphonoacetyl-L-ornithine (PALO): a convenient synthesis and investigation of influence on regulation of amino acid biosynthetic genes in Saccharomyces cerevisiae. Bioorg. Med. Chem. Let., 2011, 21, 2351-2353.
-
(2011)
Bioorg. Med. Chem. Let
, vol.21
, pp. 2351-2353
-
-
Jonson, B.1
Steadman, R.2
Patefield, K.D.3
Bunker, J.J.4
Atkin, A.L.5
Dussault, P.6
-
32
-
-
78651083689
-
Discovery of a series of phosphonic acid-containing thiazoles and orally bioavailable diamide prodrugs that lower glucose in diabetic animals through inhibition of fructose-1,6-bisphosphatase
-
Dang, Q.; Liu, Y.; Cashion, D.K.; Kasibhatla, S.R.; Jiang, T.; Taplin, F.; Jacintho, J.D.; Li, H.Q.; Sun, Z.L.; Fan, Y.; Dare, J.; Tian, F.; Li, W.Y.; Gibson, T.; Lemus, R.; van Poelje, P.D.; Potter, S.C.; Erion, M.D. Discovery of a series of phosphonic acid-containing thiazoles and orally bioavailable diamide prodrugs that lower glucose in diabetic animals through inhibition of fructose-1,6-bisphosphatase. J. Med. Chem., 2011, 54, 153-165.
-
(2011)
J. Med. Chem
, vol.54
, pp. 153-165
-
-
Dang, Q.1
Liu, Y.2
Cashion, D.K.3
Kasibhatla, S.R.4
Jiang, T.5
Taplin, F.6
Jacintho, J.D.7
Li, H.Q.8
Sun, Z.L.9
Fan, Y.10
Dare, J.11
Tian, F.12
Li, W.Y.13
Gibson, T.14
Lemus, R.15
van Poelje, P.D.16
Potter, S.C.17
Erion, M.D.18
-
33
-
-
64349124952
-
Phosphonosulfonates are potent, selective inhibitors of dehydrosqualene synthase and staphyloxanthin biosynthesis in Staphylococcus aureus
-
Song, Y.C.; Lin, F.Y.; Hensler, M.; Poveda, C.A.R.; Mukkamala, D.; Cao, R.; Wang, H.; Morita, C.T.; Pacanowska, D.G.; Nizet, V.; Oldfield, E. Phosphonosulfonates are potent, selective inhibitors of dehydrosqualene synthase and staphyloxanthin biosynthesis in Staphylococcus aureus. J. Med. Chem., 2009, 52, 976-988.
-
(2009)
J. Med. Chem
, vol.52
, pp. 976-988
-
-
Song, Y.C.1
Lin, F.Y.2
Hensler, M.3
Poveda, C.A.R.4
Mukkamala, D.5
Cao, R.6
Wang, H.7
Morita, C.T.8
Pacanowska, D.G.9
Nizet, V.10
Oldfield, E.11
-
34
-
-
33749447149
-
The synthesis and antiviral properties of acyclic nucleoside analogues with a phosphonomethoxy fragment in the side chain
-
Khandazhinskaya, A.; Yasko, M.; Shirokova E., The synthesis and antiviral properties of acyclic nucleoside analogues with a phosphonomethoxy fragment in the side chain. Curr. Med. Chem., 2006, 13(24), 2953-2980.
-
(2006)
Curr. Med. Chem
, vol.13
, Issue.24
, pp. 2953-2980
-
-
Khandazhinskaya, A.1
Yasko, M.2
Shirokova, E.3
-
35
-
-
33845335153
-
Synthesis and biological activity of phosphonated nucleosides: Part 1. Furanose, carbocyclic and heterocyclic analogues
-
Piperno, A.; Chiacchio, M.A.; Iannazzo, D.; Romeo, R. Synthesis and biological activity of phosphonated nucleosides: part 1. Furanose, carbocyclic and heterocyclic analogues. Curr. Med. Chem., 2006, 13(30), 3675-3995.
-
(2006)
Curr. Med. Chem
, vol.13
, Issue.30
, pp. 3675-3995
-
-
Piperno, A.1
Chiacchio, M.A.2
Iannazzo, D.3
Romeo, R.4
-
36
-
-
33847783139
-
Synthesis of the 5-phosphono-pent-2-en-1-yl nucleosides: A new class of antiviral acyclic nucleoside phosphonates
-
Choo, H.; Beadle, J.R.; Chong, Y.; Trahan, J.; Hostetler, K.Y. Synthesis of the 5-phosphono-pent-2-en-1-yl nucleosides: a new class of antiviral acyclic nucleoside phosphonates. Bioorg. Med. Chem., 2007, 15(4), 1771-1779.
-
(2007)
Bioorg. Med. Chem
, vol.15
, Issue.4
, pp. 1771-1779
-
-
Choo, H.1
Beadle, J.R.2
Chong, Y.3
Trahan, J.4
Hostetler, K.Y.5
-
37
-
-
77952572482
-
Synthesis and biological evaluation of inosine phosphonates
-
Abramov, M.; Herdewijn, P. Synthesis and biological evaluation of inosine phosphonates. New J. Chem., 2010, 34, 875-876.
-
(2010)
New J. Chem
, vol.34
, pp. 875-876
-
-
Abramov, M.1
Herdewijn, P.2
-
38
-
-
79955895904
-
Synthesis, Bioactivity and Crystal Structure Analysis of Diisopropyl[(4-cyanopyrazol-3-ylamino)(2-hydroxylphenyl) methyl] phosphonate
-
Hong, Y.P.; Peng, J.A.; Cao, D.R. Synthesis, Bioactivity and Crystal Structure Analysis of Diisopropyl[(4-cyanopyrazol-3-ylamino)(2-hydroxylphenyl) methyl] phosphonate. Chinese J. Struct. Chem., 2011, 30, 37-42.
-
(2011)
Chinese J. Struct. Chem
, vol.30
, pp. 37-42
-
-
Hong, Y.P.1
Peng, J.A.2
Cao, D.R.3
-
39
-
-
77956125406
-
Synthesis and antiviral bioactivity of chiral thioureas containing leucine and phosphonate moieties
-
Liu, J.Z.; Yang, S.; Li, X.Y.; Fan, H.T.; Bhadury, P.; Xu, W.M.; Wu, J.A.; Wang, Z.C. Synthesis and antiviral bioactivity of chiral thioureas containing leucine and phosphonate moieties. Molecules, 2010, 15, 5112-5123.
-
(2010)
Molecules
, vol.15
, pp. 5112-5123
-
-
Liu, J.Z.1
Yang, S.2
Li, X.Y.3
Fan, H.T.4
Bhadury, P.5
Xu, W.M.6
Wu, J.A.7
Wang, Z.C.8
-
40
-
-
79957837948
-
Novel, potent, and orally bioavailable phosphinic acid inhibitors of the hepatitis C virus NS3 protease
-
Clarke, M.O.; Chen, X.W.; Cho, A.S.; Delaney, W.E.; Doerffler, E.; Fardis, M.; Ji, M.Z.; Mertzman, M.; Pakdaman, R.; Pyun, H.J.; Rowe, T.; Yang, C.Y.; Sheng, X.C.; Kim, C.U. Novel, potent, and orally bioavailable phosphinic acid inhibitors of the hepatitis C virus NS3 protease. Bioorg. Med. Chem. Lett., 2011, 21, 3568-3572.
-
(2011)
Bioorg. Med. Chem. Lett
, vol.21
, pp. 3568-3572
-
-
Clarke, M.O.1
Chen, X.W.2
Cho, A.S.3
Delaney, W.E.4
Doerffler, E.5
Fardis, M.6
Ji, M.Z.7
Mertzman, M.8
Pakdaman, R.9
Pyun, H.J.10
Rowe, T.11
Yang, C.Y.12
Sheng, X.C.13
Kim, C.U.14
-
41
-
-
0032912771
-
The glutamate receptor ion channels
-
Dingledine, R.; Borges, K.; Bowie, D.; Traynelis, S.F. The glutamate receptor ion channels. Pharmacol. Rev., 1999, 51, 7-61.
-
(1999)
Pharmacol. Rev
, vol.51
, pp. 7-61
-
-
Dingledine, R.1
Borges, K.2
Bowie, D.3
Traynelis, S.F.4
-
42
-
-
26044432465
-
Surface properties of sulfur-and ether-linked phosphonolipids with and without purified hydrophobic lung surfactant proteins
-
Chang, Y.S.; Wang, Z.D.; Schwan, A.L.; Wang, Z.Y.; Holm, B.A.; Baatz, J.E.; Notter, R.H. Surface properties of sulfur-and ether-linked phosphonolipids with and without purified hydrophobic lung surfactant proteins. Chem. Phys. of Lipids, 2005, 137(1-2), 77-93.
-
(2005)
Chem. Phys. of Lipids
, vol.137
, Issue.1-2
, pp. 77-93
-
-
Chang, Y.S.1
Wang, Z.D.2
Schwan, A.L.3
Wang, Z.Y.4
Holm, B.A.5
Baatz, J.E.6
Notter, R.H.7
-
43
-
-
2442425372
-
Application of bacteria and fungi as biocatalysts for the preparation of optically active hydroxyphosphonates
-
Kafarski, P.; Lejczak, B. Application of bacteria and fungi as biocatalysts for the preparation of optically active hydroxyphosphonates. J. Mol. Catal. BEnzym., 2004, 29, 99-104.
-
(2004)
J. Mol. Catal. BEnzym
, vol.29
, pp. 99-104
-
-
Kafarski, P.1
Lejczak, B.2
-
44
-
-
32044435832
-
Yeast lipases: Enzyme purification, biochemical properties and gene cloning
-
Vakhlu, J.; Kour, A. Yeast lipases: enzyme purification, biochemical properties and gene cloning. Electron. J. Biotechno., 2006, 9, 69-85.
-
(2006)
Electron. J. Biotechno
, vol.9
, pp. 69-85
-
-
Vakhlu, J.1
Kour, A.2
-
45
-
-
0027405034
-
Enzymes in organic chemistry, part 1: Enantioselective hydrolysis of β-(acyloxy)phosphonates by esterolytic enzymes
-
Li, Y.; Hammerschmidt, F. Enzymes in organic chemistry, part 1: Enantioselective hydrolysis of β-(acyloxy)phosphonates by esterolytic enzymes. Tetrahedron-Asymmetr., 1993, 4, 109-120.
-
(1993)
Tetrahedron-Asymmetr
, vol.4
, pp. 109-120
-
-
Li, Y.1
Hammerschmidt, F.2
-
46
-
-
0029813748
-
Enzymes in organic chemistry, part 4: Enantioselective hydrolysis of 1-acyloxy(aryl)methyl-and 1-acyloxy(heteroaryl)methylphosphonates with lipases from Aspergillus niger and Rhizopus oryzae. A comparative study
-
Eidenhammer, G.; Hammerschmidt, F. Enzymes in organic chemistry, part 4: Enantioselective hydrolysis of 1-acyloxy(aryl)methyl-and 1-acyloxy(heteroaryl)methylphosphonates with lipases from Aspergillus niger and Rhizopus oryzae. A comparative study. Synthesis, 1996, 748-754.
-
(1996)
Synthesis
, pp. 748-754
-
-
Eidenhammer, G.1
Hammerschmidt, F.2
-
47
-
-
0030978512
-
Enzymes in organic chemistry-5: First and chemo-enzymatic synthesis of β-aminooxyphosphonic acids of high enantiomeric excess
-
Drescher, M.; Hammerschmidt, F. Enzymes in organic chemistry-5: First and chemo-enzymatic synthesis of β-aminooxyphosphonic acids of high enantiomeric excess. Tetrahedron, 1997, 53, 4627-4635.
-
(1997)
Tetrahedron
, vol.53
, pp. 4627-4635
-
-
Drescher, M.1
Hammerschmidt, F.2
-
48
-
-
0028960436
-
Enzymes in organic chemistry, part 2: Lipase-catalysed hydrolysis of 1-acyloxy-2-arylethylphosphonates and synthesis of phosphonic acid analogues of L-phenylalanine and Ltyrosine
-
Drescher, M.; Li, Y.; Hammerschmidt, F. Enzymes in organic chemistry, part 2: Lipase-catalysed hydrolysis of 1-acyloxy-2-arylethylphosphonates and synthesis of phosphonic acid analogues of L-phenylalanine and Ltyrosine. Tetrahedron, 1995, 51, 4933-4946.
-
(1995)
Tetrahedron
, vol.51
, pp. 4933-4946
-
-
Drescher, M.1
Li, Y.2
Hammerschmidt, F.3
-
49
-
-
0001027015
-
Enzymes in organic chemistry VI [1]. Enantioselective hydrolysis of 1-chloroacetoxycycloalkylmethylphosphonates with lipase AP 6 from Aspergillus niger and chemoenzymatic synthesis of chiral, nonracemic 1-aminocyclohexylmethylphosphonic acids
-
Wuggenig, F.; Hammerschmidt, F. Enzymes in organic chemistry VI [1]. Enantioselective hydrolysis of 1-chloroacetoxycycloalkylmethylphosphonates with lipase AP 6 from Aspergillus niger and chemoenzymatic synthesis of chiral, nonracemic 1-aminocyclohexylmethylphosphonic acids. Monatsh. Chem., 1998, 129, 423-436.
-
(1998)
Monatsh. Chem
, vol.129
, pp. 423-436
-
-
Wuggenig, F.1
Hammerschmidt, F.2
-
50
-
-
0033532313
-
Enzymes in organic chemistry. Part 9: Chemo-enzymatic synthesis of phosphonic acid analogues of L-valine, Lleucine, L-isoleucine, L-methionine and L-aminobutyric acid of high enantiomeric excess
-
Hammerschmidt, F.; Wuggenig, F. Enzymes in organic chemistry. Part 9: Chemo-enzymatic synthesis of phosphonic acid analogues of L-valine, Lleucine, L-isoleucine, L-methionine and L-aminobutyric acid of high enantiomeric excess. Tetrahedron-Asymmetr., 1999, 10, 1709-1721.
-
(1999)
Tetrahedron-Asymmetr
, vol.10
, pp. 1709-1721
-
-
Hammerschmidt, F.1
Wuggenig, F.2
-
51
-
-
79952929415
-
Chemoenzymatic synthesis of phosphonic acid analogues of L-lysine, L-proline, Lornithine, and L-pipecolic acid of 99→% ee-assignment of absolute configuration to (-)-Proline
-
Wuggenig, F.; Schweifer, A.; Mereiter, K.; Hammerschmidt, F. Chemoenzymatic synthesis of phosphonic acid analogues of L-lysine, L-proline, Lornithine, and L-pipecolic acid of 99→% ee-assignment of absolute configuration to (-)-Proline. Eur. J. Org. Chem., 2011, 10, 1870-1879.
-
(2011)
Eur. J. Org. Chem
, vol.10
, pp. 1870-1879
-
-
Wuggenig, F.1
Schweifer, A.2
Mereiter, K.3
Hammerschmidt, F.4
-
52
-
-
0034725687
-
Enzymes in organic chemistry. Part 10: Chemo-enzymatic synthesis of l-phosphaserine and l-phosphaisoserine and enantioseparation of aminohydroxyethylphosphonic acids by non-aqueous capillary electrophoresis with quinine carbamate as chiral ion pair agent
-
Hammerschmidt, F.; Lindner, W.; Wuggenig, F.; Zarbl, E. Enzymes in organic chemistry. Part 10: Chemo-enzymatic synthesis of l-phosphaserine and l-phosphaisoserine and enantioseparation of aminohydroxyethylphosphonic acids by non-aqueous capillary electrophoresis with quinine carbamate as chiral ion pair agent. Tetrahedron-Asymmetr., 2000, 11, 2955-2964.
-
(2000)
Tetrahedron-Asymmetr
, vol.11
, pp. 2955-2964
-
-
Hammerschmidt, F.1
Lindner, W.2
Wuggenig, F.3
Zarbl, E.4
-
53
-
-
0038433319
-
Synthesis of chiral, nonracemic β-sulfanylphosphonates and derivatives
-
Gulea, M.; Hammerschmidt, F.; Marchand, P.; Masson, S.; Pisljagic, V.; Wuggenig, F. Synthesis of chiral, nonracemic β-sulfanylphosphonates and derivatives. Tetrahedron-Asymmetr., 2003, 14, 1829-1836.
-
(2003)
Tetrahedron-Asymmetr
, vol.14
, pp. 1829-1836
-
-
Gulea, M.1
Hammerschmidt, F.2
Marchand, P.3
Masson, S.4
Pisljagic, V.5
Wuggenig, F.6
-
54
-
-
0000464704
-
Enzymatic resolution of acetoxyalkenylphosphonates and their exploitation in the chemoenzymatic synthesis of phosphonic derivatives of carbohydrates
-
Guanti, G.; Zarmetti, M.T.; Banfi, L.; Riva, R. Enzymatic resolution of acetoxyalkenylphosphonates and their exploitation in the chemoenzymatic synthesis of phosphonic derivatives of carbohydrates. Adv. Synth. Catal., 2001, 343, 682-691.
-
(2001)
Adv. Synth. Catal
, vol.343
, pp. 682-691
-
-
Guanti, G.1
Zarmetti, M.T.2
Banfi, L.3
Riva, R.4
-
55
-
-
33751499686
-
A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa
-
Kazlauskas, R.J.; Weissfloch, N.E.; Rappaport, A.T.; Cuccia, L.A. A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosa. J. Org. Chem., 1991, 56, 2656-2665.
-
(1991)
J. Org. Chem
, vol.56
, pp. 2656-2665
-
-
Kazlauskas, R.J.1
Weissfloch, N.E.2
Rappaport, A.T.3
Cuccia, L.A.4
-
56
-
-
1642576230
-
Enzymes in organic chemistry, 11: Hydrolase-catalyzed resolution of β-and β-hydroxyphosphonates and synthesis of chiral, non-racemic β-aminophosphonic acids
-
Woschek, A.; Lindner, W.; Hammerschmidt, F. Enzymes in organic chemistry, 11: Hydrolase-catalyzed resolution of β-and β-hydroxyphosphonates and synthesis of chiral, non-racemic β-aminophosphonic acids. Adv. Synth. Catal., 2003, 345, 1287-1298.
-
(2003)
Adv. Synth. Catal
, vol.345
, pp. 1287-1298
-
-
Woschek, A.1
Lindner, W.2
Hammerschmidt, F.3
-
57
-
-
0037156448
-
Candida rugosa. lipase-catalyzed enantioselective hydrolysis in organic solvents. Convenient preparation of optically pure 2-hydroxy-2-arylethanephosphonates
-
Zhang Y.; Li, Z.; Yuan, C. Candida rugosa lipase-catalyzed enantioselective hydrolysis in organic solvents. Convenient preparation of optically pure 2-hydroxy-2-arylethanephosphonates. Tetrahedron Lett., 2002, 43, 3247-3249.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 3247-3249
-
-
Zhang, Y.1
Li, Z.2
Yuan, C.3
-
58
-
-
8144231564
-
Candida rugosa lipase-catalyzed kinetic resolution of hydroxyalkanephosphonates
-
Zhang Y.; Xu, C.F.; Li, J.; Yuan, C. Candida rugosa lipase-catalyzed kinetic resolution of hydroxyalkanephosphonates. Chin. J. Chem., 2003, 21, 883-892.
-
(2003)
Chin. J. Chem
, vol.21
, pp. 883-892
-
-
Zhang, Y.1
Xu, C.F.2
Li, J.3
Yuan, C.4
-
59
-
-
0037454689
-
Enzymatic synthesis of optically active trifluoromethylated 1-and 2-hydroxyalkanephosphonates
-
Zhang Y.; Li, J.; Yuan, C. Enzymatic synthesis of optically active trifluoromethylated 1-and 2-hydroxyalkanephosphonates. Tetrahedron, 2003, 59, 473-479.
-
(2003)
Tetrahedron
, vol.59
, pp. 473-479
-
-
Zhang, Y.1
Li, J.2
Yuan, C.3
-
60
-
-
29144485899
-
A facial chemoenzymatic method for the preparation of chiral 1,2-dihydroxy-3,3,3,-trifluoropropanephosphonates
-
Yuan, C.; Li, J.; Zhang W. A facial chemoenzymatic method for the preparation of chiral 1,2-dihydroxy-3,3,3,-trifluoropropanephosphonates. J. Fluor. Chem., 2006, 127, 44-47.
-
(2006)
J. Fluor. Chem
, vol.127
, pp. 44-47
-
-
Yuan, C.1
Li, J.2
Zhang, W.3
-
61
-
-
0142165228
-
Enzymatic synthesis of phosphocarnitine, phosphogabob and fosfomycin
-
Wang, K.; Zhang, Y.; Yuan, C. Enzymatic synthesis of phosphocarnitine, phosphogabob and fosfomycin. Org. Biomol. Chem., 2003, 1, 3564-3569.
-
(2003)
Org. Biomol. Chem
, vol.1
, pp. 3564-3569
-
-
Wang, K.1
Zhang, Y.2
Yuan, C.3
-
62
-
-
0035898202
-
The synthesis of 1-hydroxy phosphonates of high enantiomeric excess using sequential asymmetric reactions: Titanium alkoxide-catalyzed P---C bond formation and kinetic resolution
-
Rowe, B.J.; Spilling, C.D. The synthesis of 1-hydroxy phosphonates of high enantiomeric excess using sequential asymmetric reactions: titanium alkoxide-catalyzed P---C bond formation and kinetic resolution. Tetrahedron-Asymmetr., 2001, 12, 1701-1708.
-
(2001)
Tetrahedron-Asymmetr
, vol.12
, pp. 1701-1708
-
-
Rowe, B.J.1
Spilling, C.D.2
-
63
-
-
0039906733
-
Synthesis of P-chiral, non-racemic phosphinylacetates via enzymatic resolution of racemates
-
Kieńbasinski, P.; Aurawiżski, R.; Pietrusiewicz, K.M.; Zabńocka M.; Mikońajczyk, M. Synthesis of P-chiral, non-racemic phosphinylacetates via enzymatic resolution of racemates. Polish J. Chem., 1998, 72, 564-572.
-
(1998)
Polish J. Chem
, vol.72
, pp. 564-572
-
-
Kieńbasinski, P.1
Aurawizski, R.2
Pietrusiewicz, K.M.3
Zabńocka, M.4
Mikońajczyk, M.5
-
64
-
-
0040499698
-
Enzyme-promoted kinetic resolution of racemic, P-chiral phosphonyl and phosphorylacetates
-
Kieńbasinski P.; Góralczyk, P.; Mikońajczyk, M.; Wieczorek M.W.; Majzner, W.R. Enzyme-promoted kinetic resolution of racemic, P-chiral phosphonyl and phosphorylacetates. Tetrahedron-Asymmetr, 1998, 9, 2641-2650.
-
(1998)
Tetrahedron-Asymmetr
, vol.9
, pp. 2641-2650
-
-
Kieńbasinski, P.1
Góralczyk, P.2
Mikońajczyk, M.3
Wieczorek, M.W.4
Majzner, W.R.5
-
65
-
-
4344716612
-
Lipase-catalyzed kinetic resolution of β-hydroxy-H-phosphinates
-
Yamagashi, T.; Miyamae, T.; Yokomatsu, T.; Shibuya, S. Lipase-catalyzed kinetic resolution of β-hydroxy-H-phosphinates. Tetrahedron Lett., 2004, 45, 6713-6716.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 6713-6716
-
-
Yamagashi, T.1
Miyamae, T.2
Yokomatsu, T.3
Shibuya, S.4
-
66
-
-
67651092279
-
Enzymatic resolution of β-hydroxyphosphinates with two stereogenic centers and determination of absolute configuration of stereoisomers obtained
-
Majewska, P.; Doskocz, M.; Lejczak, B.; Kafarski, P. Enzymatic resolution of β-hydroxyphosphinates with two stereogenic centers and determination of absolute configuration of stereoisomers obtained. Tetrahedron-Asymmetr., 2009, 20, 1568-1574.
-
(2009)
Tetrahedron-Asymmetr
, vol.20
, pp. 1568-1574
-
-
Majewska, P.1
Doskocz, M.2
Lejczak, B.3
Kafarski, P.4
-
67
-
-
33750507221
-
An approach for the synthesis and assignment of absolute configuration of all enantiomers of etyl hydroxy (phenyl)methane(P-phenyl)phosphinate
-
Majewska, P.; Kafarski, P.; Lejczak, B. An approach for the synthesis and assignment of absolute configuration of all enantiomers of etyl hydroxy (phenyl)methane(P-phenyl)phosphinate. Tetrahedron-Asymmetr., 2006, 17, 2697-2701.
-
(2006)
Tetrahedron-Asymmetr
, vol.17
, pp. 2697-2701
-
-
Majewska, P.1
Kafarski, P.2
Lejczak, B.3
-
68
-
-
77956216085
-
Enzymatic resolution of ethyl-hydroxyphosphinates in a modified reaction environment
-
Majewska, P.; Lejczak, B.; Kafarski, P. Enzymatic resolution of ethyl-hydroxyphosphinates in a modified reaction environment. Phosphoru, Sulfur, 2010, 185, 1915-1921.
-
(2010)
Phosphoru, Sulfur
, vol.185
, pp. 1915-1921
-
-
Majewska, P.1
Lejczak, B.2
Kafarski, P.3
-
69
-
-
17144387568
-
Lipase-catalysed resolution of 1-hydroxyethane-P-phenylphosphinates
-
Majewska P.; Kafarski, P.; Lejczak, B. Lipase-catalysed resolution of 1-hydroxyethane-P-phenylphosphinates. Polish J. Chem., 2005, 79, 561-566.
-
(2005)
Polish J. Chem
, vol.79
, pp. 561-566
-
-
Majewska, P.1
Kafarski, P.2
Lejczak, B.3
-
70
-
-
0032895010
-
Enantioselective hydrolysis of 1-butyryloxyalkylphosphonates by lipolytic microorganisms: Pseudomonas fluorescens and Penicillium citrinum
-
Skwarczyski, M.; Lejczak, B.; Kafarski, P. Enantioselective hydrolysis of 1-butyryloxyalkylphosphonates by lipolytic microorganisms: Pseudomonas fluorescens and Penicillium citrinum. Chirality, 1999, 11, 109-114.
-
(1999)
Chirality
, vol.11
, pp. 109-114
-
-
Skwarczyski, M.1
Lejczak, B.2
Kafarski, P.3
-
71
-
-
33750507221
-
An approach for the synthesis and assignment of absolute configuration of all enantiomers of etyl hydroxy(phenyl)methane(P-phenyl)phosphinate
-
Majewska P.; Kafarski, P.; Lejczak, B.; Bryndal, I.; Lis, T. An approach for the synthesis and assignment of absolute configuration of all enantiomers of etyl hydroxy(phenyl)methane(P-phenyl)phosphinate. Tetrahedron-Asymmetr., 2006, 17, 2697-2701.
-
(2006)
Tetrahedron-Asymmetr
, vol.17
, pp. 2697-2701
-
-
Majewska, P.1
Kafarski, P.2
Lejczak, B.3
Bryndal, I.4
Lis, T.5
-
72
-
-
0142196043
-
The first enzymatic desymmetrizations of prochiral phosphine oxides
-
Kiebasiski, P.; Urawiski, R.; Albrycht, M.; Mikoajczyk, M. The first enzymatic desymmetrizations of prochiral phosphine oxides. Tetrahedron-Asymmetr., 2003, 14, 3379-3384.
-
(2003)
Tetrahedron-Asymmetr
, vol.14
, pp. 3379-3384
-
-
Kiebasiski, P.1
Urawiski, R.2
Albrycht, M.3
Mikoajczyk, M.4
-
73
-
-
34748909424
-
Enzyme-promoted desymmetrization of prochiral bis(cyanomethyl)phenylphosphine oxide
-
Kiebasinski, P.; Rachwalski, M.; Kwiatkowska, M.; Mikoajczyk, M.; Wieczorek, W.; Szyrej, M.; Siero, L.; Rutjes, P. Enzyme-promoted desymmetrization of prochiral bis(cyanomethyl)phenylphosphine oxide. Tetrahedron-Asymmetr., 2007, 18, 2108-2112.
-
(2007)
Tetrahedron-Asymmetr
, vol.18
, pp. 2108-2112
-
-
Kiebasinski, P.1
Rachwalski, M.2
Kwiatkowska, M.3
Mikoajczyk, M.4
Wieczorek, W.5
Szyrej, M.6
Siero, L.7
Rutjes, P.8
-
75
-
-
34547180822
-
Nitrilase-catalyzed selective hydrolysis of dinitriles and green access to the cyanocarboxylic acids of pharmaceutical importance
-
Zhu, D.; Mukherjee, C.; Biehl, E.R.; Huaa, L. Nitrilase-catalyzed selective hydrolysis of dinitriles and green access to the cyanocarboxylic acids of pharmaceutical importance. Adv. Synth. Catal., 2007, 349,1667-1670.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 1667-1670
-
-
Zhu, D.1
Mukherjee, C.2
Biehl, E.R.3
Huaa, L.4
-
76
-
-
0035842873
-
Biocatalytic syntheses of chiral non-racemic 2-hydroxyalkanephosphonates
-
Urawiski, R.; Nakamura, K.; Drabowicz, J.; Kiebasinski, P.; Mikoajczyk, M. Biocatalytic syntheses of chiral non-racemic 2-hydroxyalkanephosphonates. Tetrahedron-Asymmetr., 2001, 12, 3139-3145.
-
(2001)
Tetrahedron-Asymmetr
, vol.12
, pp. 3139-3145
-
-
Urawiski, R.1
Nakamura, K.2
Drabowicz, J.3
Kiebasinski, P.4
Mikoajczyk, M.5
-
77
-
-
0037041526
-
Kinetic resolution of hydroxyalkanephosphonates catalyzed by Candida antarctica lipase B in organic media
-
Hang, Y.; Yuan, C.; Li, Z. Kinetic resolution of hydroxyalkanephosphonates catalyzed by Candida antarctica lipase B in organic media. Tetrahedron, 2002, 58, 2973-2978.
-
(2002)
Tetrahedron
, vol.58
, pp. 2973-2978
-
-
Hang, Y.1
Yuan, C.2
Li, Z.3
-
78
-
-
0037421269
-
Enzymatic synthesis of optically active hydroxy-ketoalkanephosphonates
-
Zhang, Y.; Xy, C.; Li, J.; Yuan, C. Enzymatic synthesis of optically active hydroxy-ketoalkanephosphonates. Tetrahedron-Asymmetr., 2003, 14, 63-70.
-
(2003)
Tetrahedron-Asymmetr
, vol.14
, pp. 63-70
-
-
Zhang, Y.1
Xy, C.2
Li, J.3
Yuan, C.4
-
79
-
-
1842528077
-
Enzymatic synthesis of optically active β-chloro--hydroxy-ketoalkanephosphonates and reactions thereof
-
Xu, C.; Yuan, C. Enzymatic synthesis of optically active β-chloro--hydroxy-ketoalkanephosphonates and reactions thereof. Tetrahedron, 2004, 60, 3883-3892.
-
(2004)
Tetrahedron
, vol.60
, pp. 3883-3892
-
-
Xu, C.1
Yuan, C.2
-
80
-
-
0037941143
-
An efficient route to chiral alpha-and betahydroxyalkanephosphonates
-
Pamies, O.; Backvall, J.E. An efficient route to chiral alpha-and betahydroxyalkanephosphonates. J. Org. Chem., 2003, 68, 4815-4818.
-
(2003)
J. Org. Chem
, vol.68
, pp. 4815-4818
-
-
Pamies, O.1
Backvall, J.E.2
-
81
-
-
0036828077
-
Chemoenzymatic synthesis of phosphocarnitine enantiomers
-
Mikoajczyk, M.; Nuczak, J.; Kiebasiαski, P. Chemoenzymatic synthesis of phosphocarnitine enantiomers. J. Org. Chem., 2002, 67, 7872-7875.
-
(2002)
J. Org. Chem
, vol.67
, pp. 7872-7875
-
-
Mikoajczyk, M.1
Nuczak, J.2
Kiebasiαski, P.3
-
82
-
-
33646891552
-
Lipasemediated kinetic resolution of racemic and desymmetrization of prochiral organophosphorus P-boranes
-
Kiebasinski, P.; Albrycht, M.; Urawiski, R.; Mikoajczyk, M. Lipasemediated kinetic resolution of racemic and desymmetrization of prochiral organophosphorus P-boranes. J. Mol. Catal. B-Enzym., 2006, 39, 45-49.
-
(2006)
J. Mol. Catal. B-Enzym
, vol.39
, pp. 45-49
-
-
Kiebasinski, P.1
Albrycht, M.2
Urawiski, R.3
Mikoajczyk, M.4
-
83
-
-
0141888284
-
First enzymatic resolution of a phosphaneborane complex
-
Faure, B.; Iacazio, G.; Maffei, M. First enzymatic resolution of a phosphaneborane complex. J. Mol. Catal. B-Enzym., 2003, 26, 29-32.
-
(2003)
J. Mol. Catal. B-Enzym
, vol.26
, pp. 29-32
-
-
Faure, B.1
Iacazio, G.2
Maffei, M.3
-
84
-
-
0032544784
-
Lipase-promoted kinetic resolution of racemic, P-chiral hydroxymethylphosphonates and phosphinates
-
Kiebasinski, P.; Omelaczuk, J.; Mikoajczyk, M. Lipase-promoted kinetic resolution of racemic, P-chiral hydroxymethylphosphonates and phosphinates. Tetrahedron-Asymmetr., 1998, 9, 3283-3287.
-
(1998)
Tetrahedron-Asymmetr
, vol.9
, pp. 3283-3287
-
-
Kiebasinski, P.1
Omelaczuk, J.2
Mikoajczyk, M.3
-
85
-
-
0037007651
-
Enzymatic reactions in ionic liquids: Lipase-catalysed kinetic resolution of racemic, Pchiral hydroxymethanephosphinates and hydroxymethylphosphine oxides
-
Kiebasinski, P.; Albrycht, M.; Uczak, J.; Mikoajczyk, M. Enzymatic reactions in ionic liquids: lipase-catalysed kinetic resolution of racemic, Pchiral hydroxymethanephosphinates and hydroxymethylphosphine oxides. Tetrahedron-Asymmetr., 2002, 13, 735-738.
-
(2002)
Tetrahedron-Asymmetr
, vol.13
, pp. 735-738
-
-
Kiebasinski, P.1
Albrycht, M.2
Uczak, J.3
Mikoajczyk, M.4
-
86
-
-
20444362064
-
Supercritical carbon dioxide as a reaction medium for enzymatic kinetic resolution of P-chiral hydroxymethanephosphinates
-
Albrycht, M.; Kiebasinski, P.; Drabowicz, J.; Mikoajczyk, M.; Matsuda, T.; Harada, T.; Nakamura, K. Supercritical carbon dioxide as a reaction medium for enzymatic kinetic resolution of P-chiral hydroxymethanephosphinates. Tetrahedron-Asymmetr., 2005, 16, 2015-2018.
-
(2005)
Tetrahedron-Asymmetr
, vol.16
, pp. 2015-2018
-
-
Albrycht, M.1
Kiebasinski, P.2
Drabowicz, J.3
Mikoajczyk, M.4
Matsuda, T.5
Harada, T.6
Nakamura, K.7
-
87
-
-
0037467852
-
Synthesis of bifunctional Pchiral hydroxy phosphinates; lipase-catalyzed stereoselective acylation of ethyl (1-hydroxyalkyl)phenylphosphinates
-
Shioji, K.; Tashiro, A.; Shibata, S.; Okuma, K. Synthesis of bifunctional Pchiral hydroxy phosphinates; lipase-catalyzed stereoselective acylation of ethyl (1-hydroxyalkyl)phenylphosphinates. Tetrahedron Lett., 2003, 44, 1103-1105.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1103-1105
-
-
Shioji, K.1
Tashiro, A.2
Shibata, S.3
Okuma, K.4
-
88
-
-
23044533691
-
Synthesis of phosphine analog of glutamylglycine
-
Ragulin, W. Synthesis of phosphine analog of glutamylglycine. Russ. J. Gen. Chem., 2001, 71, 1823-1824.
-
(2001)
Russ. J. Gen. Chem
, vol.71
, pp. 1823-1824
-
-
Ragulin, W.1
-
89
-
-
0025843366
-
Preparation of optically active 1-aminoalkylphosphonic acids by stereoselective enzymatic hydrolysis of racemic N-acylated 1-aminoalkylphosphonic acids
-
Solodenko, V.; Kasheva, N.; Kukhar, V.; Kozlova, E.; Mironenko, D.; Svedas, V. Preparation of optically active 1-aminoalkylphosphonic acids by stereoselective enzymatic hydrolysis of racemic N-acylated 1-aminoalkylphosphonic acids. Tetrahedron, 1991, 47, 3989-3998.
-
(1991)
Tetrahedron
, vol.47
, pp. 3989-3998
-
-
Solodenko, V.1
Kasheva, N.2
Kukhar, V.3
Kozlova, E.4
Mironenko, D.5
Svedas, V.6
-
90
-
-
24744466043
-
Enzymatic synthesis of the enantiomers of 2-amino-2-methyl-4-phosphonobutyric acid
-
Ragulin, W. Enzymatic synthesis of the enantiomers of 2-amino-2-methyl-4-phosphonobutyric acid. Russ. J. Gen. Chem., 2004, 74, 1297-1299.
-
(2004)
Russ. J. Gen. Chem
, vol.74
, pp. 1297-1299
-
-
Ragulin, W.1
-
91
-
-
0028868413
-
Enantioselective reduction of diethyl 2-oxolakylphospohonates by Baker's Yeast
-
Ymaczyk-Duda, E.; Lejczak, B.; Kafarski, P.; Grimaud, J.; Fisher, P. Enantioselective reduction of diethyl 2-oxolakylphospohonates by Baker's Yeast. Tetrahedron, 1995, 51, 11809-11814.
-
(1995)
Tetrahedron
, vol.51
, pp. 11809-11814
-
-
Ymaczyk-Duda, E.1
Lejczak, B.2
Kafarski, P.3
Grimaud, J.4
Fisher, P.5
-
92
-
-
0342546040
-
Reductive biotransformation of diethyl beta-, gamma-and delta-oxoalkylphosphonates by cells of baker's yeast
-
Ymaczyk-Duda, E.; Kafarski, P.; Lejczak, B. Reductive biotransformation of diethyl beta-, gamma-and delta-oxoalkylphosphonates by cells of baker's yeast. Enzyme Microb. Tech., 2000, 26, 265-270.
-
(2000)
Enzyme Microb. Tech
, vol.26
, pp. 265-270
-
-
Ymaczyk-Duda, E.1
Kafarski, P.2
Lejczak, B.3
-
93
-
-
0036020839
-
Enantioselective reduction of 2-ketoalkanephosphonate by baker's yeast
-
Wang, K.; Li, Z.; Yuan, C. Enantioselective reduction of 2-ketoalkanephosphonate by baker's yeast Phosphorus Sulfur, 2002, 177, 1797-1800.
-
(2002)
Phosphorus Sulfur
, vol.177
, pp. 1797-1800
-
-
Wang, K.1
Li, Z.2
Yuan, C.3
-
94
-
-
0036810641
-
Stereoselective synthesis of phosphorus analogs of (R)-carnitine and (R)-gabob
-
Yuan, C.; Wang, K.; Li, J.; Li, Z. Stereoselective synthesis of phosphorus analogs of (R)-carnitine and (R)-gabob. Phosphorus Sulfur, 2002, 177, 2391-2397.
-
(2002)
Phosphorus Sulfur
, vol.177
, pp. 2391-2397
-
-
Yuan, C.1
Wang, K.2
Li, J.3
Li, Z.4
-
95
-
-
0036862345
-
Application of fungi as biocatalysts for the reduction of diethyl 1-oxoalkylphosphonates in anhydrous hexane
-
Brzeziska-Rodak, M.; Ymaczyk-Duda, E.; Kafarski, P.; Lejczak, B. Application of fungi as biocatalysts for the reduction of diethyl 1-oxoalkylphosphonates in anhydrous hexane. Biotechnol. Prog., 2002, 18, 1287-1291.
-
(2002)
Biotechnol. Prog
, vol.18
, pp. 1287-1291
-
-
Brzeziska-Rodak, M.1
Ymaczyk-Duda, E.2
Kafarski, P.3
Lejczak, B.4
-
96
-
-
17944363245
-
Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts
-
Ymaczyk-Duda, E.; Klimek-Ochab, M.; Kafarski, P.; Lejczak, B. Stereochemical control of biocatalytic asymmetric reduction of diethyl 2-oxopropylphosphonate employing yeasts. J. Organomet. Chem., 2005, 690, 2593-2596.
-
(2005)
J. Organomet. Chem
, vol.690
, pp. 2593-2596
-
-
Ymaczyk-Duda, E.1
Klimek-Ochab, M.2
Kafarski, P.3
Lejczak, B.4
-
97
-
-
79954420578
-
Application of the Beauveria bassiana strain for the enantioselective oxidation of the diethyl 1-hydroxy-1-phenylmethanephosphonate
-
Ymaczyk-Duda, E.; Brzeziska-Rodak, M.; Klimek-Ochab, M.; Lejczak, B. Application of the Beauveria bassiana strain for the enantioselective oxidation of the diethyl 1-hydroxy-1-phenylmethanephosphonate. Curr. Microbiol., 2011, 62, 1168-1172.
-
(2011)
Curr. Microbiol
, vol.62
, pp. 1168-1172
-
-
Ymaczyk-Duda, E.1
Brzeziska-Rodak, M.2
Klimek-Ochab, M.3
Lejczak, B.4
-
98
-
-
39949084138
-
Effective fungal catalyzed synthesis of P-chiral organophosphorus compounds
-
Klimek-Ochab, M.; Ymaczyk-Duda, E.; Brzeziska-Rodak, M.; Majewska, P.; Lejczak, B. Effective fungal catalyzed synthesis of P-chiral organophosphorus compounds. Tetrahedon-Asymmetr., 2008, 19, 450-453.
-
(2008)
Tetrahedon-Asymmetr
, vol.19
, pp. 450-453
-
-
Klimek-Ochab, M.1
Ymaczyk-Duda, E.2
Brzeziska-Rodak, M.3
Majewska, P.4
Lejczak, B.5
-
99
-
-
0036903981
-
On the transformation of (S)-2-hydroxypropyl-phosphonic acid into fosfomycin in Streptomyces fradiae-A unique method of epoxide ring formation
-
Woschek, A.; Wuggenig, F.; Peti, W.; Hammerschmidt, F. On the transformation of (S)-2-hydroxypropyl-phosphonic acid into fosfomycin in Streptomyces fradiae-A unique method of epoxide ring formation. ChemBioChem., 2002, 3, 829-835.
-
(2002)
ChemBioChem
, vol.3
, pp. 829-835
-
-
Woschek, A.1
Wuggenig, F.2
Peti, W.3
Hammerschmidt, F.4
-
100
-
-
43549097791
-
On the conversion of structural analogues of (S)-2-hydroxypropylphosphonic acid to epoxides by the final enzyme of fosfomycin biosynthesis in S. fradiae
-
Schweifer, A.; Hammerschmidt, F. On the conversion of structural analogues of (S)-2-hydroxypropylphosphonic acid to epoxides by the final enzyme of fosfomycin biosynthesis in S. fradiae. Bioorg. Med. Chem., 2008, 18, 3056-3059.
-
(2008)
Bioorg. Med. Chem
, vol.18
, pp. 3056-3059
-
-
Schweifer, A.1
Hammerschmidt, F.2
-
101
-
-
79960790656
-
Biocatalytic resolution of enantiomeric mixtures of 1-aminoethanephosphonic acid
-
Brzeziska-Rodak, M.; Klimek-Ochab, M.; Ymaczyk-Duda, E.; Kafarski, P. Biocatalytic resolution of enantiomeric mixtures of 1-aminoethanephosphonic acid. Molecules, 2011, 16, 5896-5904.
-
(2011)
Molecules
, vol.16
, pp. 5896-5904
-
-
Brzeziska-Rodak, M.1
Klimek-Ochab, M.2
Ymaczyk-Duda, E.3
Kafarski, P.4
-
102
-
-
41449090012
-
Chiral O-phosphorylated derivative of 2-hydroxy-2-phenylethylphosphonate as a valuable product of microbial biotransformation of diethyl 2-oxo-2-phenylethylphosphonate
-
Ymaczyk-Duda, E.; Brzeziska-Rodak, M.; Klimek-Ochab, M.; Latajka, R.; Kafarski, P.; Lejczak, B. Chiral O-phosphorylated derivative of 2-hydroxy-2-phenylethylphosphonate as a valuable product of microbial biotransformation of diethyl 2-oxo-2-phenylethylphosphonate. J. Mol. Catal. BEnzym., 2008, 52, 74-77.
-
(2008)
J. Mol. Catal. BEnzym
, vol.52
, pp. 74-77
-
-
Ymaczyk-Duda, E.1
Brzeziska-Rodak, M.2
Klimek-Ochab, M.3
Latajka, R.4
Kafarski, P.5
Lejczak, B.6
-
103
-
-
34250858893
-
Enzymatic synthesis of phosphonomethyl oligonucleotides by therminator polymerase
-
Renders, M.; Emmerechts, G.; Rozewski, J.; Krecmerova, M.; Holy, A.; Herdewijn, P. Enzymatic synthesis of phosphonomethyl oligonucleotides by therminator polymerase. Angew. Chem. Int. Ed., 2007, 46, 2501-2504.
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 2501-2504
-
-
Renders, M.1
Emmerechts, G.2
Rozewski, J.3
Krecmerova, M.4
Holy, A.5
Herdewijn, P.6
-
104
-
-
58049192973
-
Enzyme-catalyzed synthesis of isosteric phosphono-analogues of sugar nucleotides
-
Beaton, S.A.; Huestis, M.; P.; Sadeghi-Khomami, A.; Thomas, N.R.; Jakeman, D.L. Enzyme-catalyzed synthesis of isosteric phosphono-analogues of sugar nucleotides. Chem. Commun., 2009, 2, 238-240.
-
(2009)
Chem. Commun
, vol.2
, pp. 238-240
-
-
Beaton, S.A.1
Huestis, M.P.2
Sadeghi-Khomami, A.3
Thomas, N.R.4
Jakeman, D.L.5
-
105
-
-
77957900135
-
Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analogue of UDPGalp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase
-
Sarathy, K.P.; Sadeghi-Khomani, A.; Slowski, K.; Kotake, T.; Thomas, N.R.; Jakeman, D.L.; Sanders, D.A.R. Chemoenzymatic synthesis, inhibition studies, and X-ray crystallographic analysis of the phosphono analogue of UDPGalp as an inhibitor and mechanistic probe for UDP-galactopyranose mutase. J. Mol. Biol., 2010, 403, 578-590.
-
(2010)
J. Mol. Biol
, vol.403
, pp. 578-590
-
-
Sarathy, K.P.1
Sadeghi-Khomani, A.2
Slowski, K.3
Kotake, T.4
Thomas, N.R.5
Jakeman, D.L.6
Sanders, D.A.R.7
-
106
-
-
0034701465
-
Phosphonic derivatives of carbohydrates: Chemoenzymatic synthesis
-
Guanti, G.; Banfi, L.; Zannetti, M.T. Phosphonic derivatives of carbohydrates: chemoenzymatic synthesis. Tetrahedron Lett., 2000, 41, 3181-3185.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 3181-3185
-
-
Guanti, G.1
Banfi, L.2
Zannetti, M.T.3
-
107
-
-
0035906055
-
Chemical-enzymatic synthesis of azasugar phosphonic acids as glycosyl phosphate surrogates
-
Schuster, M.; He, W.-F.; Blechert, S. Chemical-enzymatic synthesis of azasugar phosphonic acids as glycosyl phosphate surrogates. Tetrahedron Lett., 2001, 42, 2289-2291.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 2289-2291
-
-
Schuster, M.1
He, W.-F.2
Blechert, S.3
-
108
-
-
0008328489
-
Chemical-enzymatic synthesis of iminocyclitol phosphonic acids
-
Mitchel, M.; Qaio, L.; Wong, C.-H. Chemical-enzymatic synthesis of iminocyclitol phosphonic acids. Adv. Synth. Catal., 2001, 343, 596-599.
-
(2001)
Adv. Synth. Catal
, vol.343
, pp. 596-599
-
-
Mitchel, M.1
Qaio, L.2
Wong, C.-H.3
-
109
-
-
0031398920
-
Practical synthesis of 4-hydroxy-3-oxobutylphosphonic acid and its evaluation as a bio-isosteric substrate of DHAP aldolase
-
Arth, H.L.; Fessner, W.D. Practical synthesis of 4-hydroxy-3-oxobutylphosphonic acid and its evaluation as a bio-isosteric substrate of DHAP aldolase. Carbohydrate Res., 1997, 305, 313-321.
-
(1997)
Carbohydrate Res
, vol.305
, pp. 313-321
-
-
Arth, H.L.1
Fessner, W.D.2
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