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1
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0029103383
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Dynamic kinetic resolution
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Ward R.S. Dynamic kinetic resolution. Tetrahedron Asymmetry. 6:1995;1475-1490.
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(1995)
Tetrahedron Asymmetry
, vol.6
, pp. 1475-1490
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Ward, R.S.1
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2
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0030751193
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Enzymes and transition metal complexes in tandem - A new concept for dynamic kinetic resolution
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Stürmer R. Enzymes and transition metal complexes in tandem - A new concept for dynamic kinetic resolution. Angew Chem Int Ed Engl. 36:1997;1173-1174.
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(1997)
Angew Chem Int Ed Engl
, vol.36
, pp. 1173-1174
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Stürmer, R.1
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4
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0033637451
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Dynamic resolution and stereoinversion of secondary alcohols by chem-enzymatic processes
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Azerad R., Buisson D. Dynamic resolution and stereoinversion of secondary alcohols by chem-enzymatic processes. Curr Opin Biotechnol. 11:2000;565-571.
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(2000)
Curr Opin Biotechnol
, vol.11
, pp. 565-571
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Azerad, R.1
Buisson, D.2
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5
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57249106473
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Racemisation in asymmetric synthesis. Dynamic kinetic resolution and related processes in enzyme and metal catalysis
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An excellent and comprehensive account of DKR by coupled enzyme-metal catalysis.
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Huerta F.F., Minidis A.B.E., Bäckvall J.E. Racemisation in asymmetric synthesis. Dynamic kinetic resolution and related processes in enzyme and metal catalysis. Chem Soc Rev. 30:2001;321-331. An excellent and comprehensive account of DKR by coupled enzyme-metal catalysis.
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(2001)
Chem Soc Rev
, vol.30
, pp. 321-331
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Huerta, F.F.1
Minidis, A.B.E.2
Bäckvall, J.E.3
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6
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0029968623
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Dynamic kinetic resolution with enzyme and palladium combinations
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Allen J.V., Williams J.M.J. Dynamic kinetic resolution with enzyme and palladium combinations. Tetrahedron Lett. 37:1996;1859-1862.
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(1996)
Tetrahedron Lett
, vol.37
, pp. 1859-1862
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Allen, J.V.1
Williams, J.M.J.2
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7
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0030583519
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Catalytic racemisation of alcohols: Application to enzymatic resolution reactions
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Dinh P.M., Howarth J.A., Hudnott A.R., Williams J.M.J., Harris W. Catalytic racemisation of alcohols: application to enzymatic resolution reactions. Tetrahedron Lett. 37:1996;7623-7626.
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(1996)
Tetrahedron Lett
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, pp. 7623-7626
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Dinh, P.M.1
Howarth, J.A.2
Hudnott, A.R.3
Williams, J.M.J.4
Harris, W.5
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8
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0001079960
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Lipase-catalyzed dynamic kinetic resolution of chiral amines: Use of palladium as the racemization catalyst
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Reetz M.T., Schimossek K. Lipase-catalyzed dynamic kinetic resolution of chiral amines: use of palladium as the racemization catalyst. Chimia. 50:1996;668-669.
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(1996)
Chimia
, vol.50
, pp. 668-669
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Reetz, M.T.1
Schimossek, K.2
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9
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0030789621
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Enzymatic resolution of alcohols coupled with ruthenium-catalyzed racemization of the substrate alcohol
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Larsson A.L.E., Persson B.A., Bäckvall J.E. Enzymatic resolution of alcohols coupled with ruthenium-catalyzed racemization of the substrate alcohol. Angew Chem Int Ed Engl. 36:1997;1211-1212.
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(1997)
Angew Chem Int Ed Engl
, vol.36
, pp. 1211-1212
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Larsson, A.L.E.1
Persson, B.A.2
Bäckvall, J.E.3
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10
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0033518869
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Ruthenium- and enzyme-catalyzed dynamic kinetic resolution of secondary alcohols
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This paper describes the first practical use of enzyme-metal combo catalysis for the deracemization of secondary alcohols.
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Persson B.A., Larsson A.L.E., Ray M.L., Bäckvall J.E. Ruthenium- and enzyme-catalyzed dynamic kinetic resolution of secondary alcohols. J Am Chem Soc. 121:1999;1645-1650. This paper describes the first practical use of enzyme-metal combo catalysis for the deracemization of secondary alcohols.
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(1999)
J Am Chem Soc
, vol.121
, pp. 1645-1650
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Persson, B.A.1
Larsson, A.L.E.2
Ray, M.L.3
Bäckvall, J.E.4
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11
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0032581651
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Efficient catalytic racemization of secondary alcohols
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Koh J.H., Jeong H.M., Park J. Efficient catalytic racemization of secondary alcohols. Tetrahedron Lett. 39:1998;5545-5548.
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(1998)
Tetrahedron Lett
, vol.39
, pp. 5545-5548
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Koh, J.H.1
Jeong, H.M.2
Park, J.3
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12
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0033588195
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Enzymatic resolution of secondary alcohols coupled with ruthenium-catalyzed racemization without hydrogen
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This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of secondary alcohols.
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Koh J.H., Jung H.M., Kim M.J., Park J. Enzymatic resolution of secondary alcohols coupled with ruthenium-catalyzed racemization without hydrogen. Tetrahedron Lett. 40:1999;6281-6284. This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of secondary alcohols.
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(1999)
Tetrahedron Lett
, vol.40
, pp. 6281-6284
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Koh, J.H.1
Jung, H.M.2
Kim, M.J.3
Park, J.4
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13
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0034720945
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Dynamic kinetic resolution of allylic alcohols mediated by ruthenium- and lipase-based catalysts
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This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of allylic alcohols.
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Lee D., Huh E.A., Kim M.J., Jung H.M., Koh J.H., Park J. Dynamic kinetic resolution of allylic alcohols mediated by ruthenium- and lipase-based catalysts. Org Lett. 2:2000;2377-2379. This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of allylic alcohols.
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(2000)
Org Lett
, vol.2
, pp. 2377-2379
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Lee, D.1
Huh, E.A.2
Kim, M.J.3
Jung, H.M.4
Koh, J.H.5
Park, J.6
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14
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0037007916
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Aminocyclopentadienyl ruthenium chloride: Catalytic racemization and dynamic kinetic resolution of alcohols at ambient temperature
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This work describes the use of a ruthenium catalyst that is highly active at room temperature as the racemization catalyst for the deracemization of secondary alcohols.
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Choi J.H., Kim Y.H., Nam S.H., Shin S.T., Kim M.J., Park J. Aminocyclopentadienyl ruthenium chloride: catalytic racemization and dynamic kinetic resolution of alcohols at ambient temperature. Angew Chem Int Ed Engl. 41:2002;2373-2376. This work describes the use of a ruthenium catalyst that is highly active at room temperature as the racemization catalyst for the deracemization of secondary alcohols.
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(2002)
Angew Chem Int Ed Engl
, vol.41
, pp. 2373-2376
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Choi, J.H.1
Kim, Y.H.2
Nam, S.H.3
Shin, S.T.4
Kim, M.J.5
Park, J.6
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15
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0037094746
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Efficient ruthenium-catalyzed racemization of secondary alcohols: Application to dynamic kinetic resolution
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Dijksman A., Elzinga J.M., Li Y.X., Arends I.W.C.E., Sheldon R.A. Efficient ruthenium-catalyzed racemization of secondary alcohols: application to dynamic kinetic resolution. Tetrahedron Asymmetry. 13:2002;879-884.
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(2002)
Tetrahedron Asymmetry
, vol.13
, pp. 879-884
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Dijksman, A.1
Elzinga, J.M.2
Li, Y.X.3
Arends, I.W.C.E.4
Sheldon, R.A.5
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16
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0041402634
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Dynamic kinetic resolution of α-hydroxy acid esters
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Describes the use of a ruthenium-catalyzed racemization for the deracemization of hydroxy esters.
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Persson B.A., Laxmi S.Y.R., Bäckvall J.E. Dynamic kinetic resolution of α-hydroxy acid esters. Org Lett. 2:2000;1037-1040. Describes the use of a ruthenium-catalyzed racemization for the deracemization of hydroxy esters.
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(2000)
Org Lett
, vol.2
, pp. 1037-1040
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Persson, B.A.1
Laxmi, S.Y.R.2
Bäckvall, J.E.3
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17
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0035912310
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Enantioselective synthesis of β-hydroxy acid derivatives via a one-pot aldol reaction-dynamic kinetic resolution
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Huerta F.F., Bäckvall J.E. Enantioselective synthesis of β-hydroxy acid derivatives via a one-pot aldol reaction-dynamic kinetic resolution. Org Lett. 3:2001;1209-1212.
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(2001)
Org Lett
, vol.3
, pp. 1209-1212
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Huerta, F.F.1
Bäckvall, J.E.2
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19
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0037154874
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Enzymatic kinetic resolution and chemoenzymatic dynamic kinetic resolution of δ-hydroxy esters. An efficient route to chiral δ-lactones
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Pàmies O., Bäckvall J.E. Enzymatic kinetic resolution and chemoenzymatic dynamic kinetic resolution of δ-hydroxy esters. An efficient route to chiral δ-lactones. J Org Chem. 67:2002;1261-1265.
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(2002)
J Org Chem
, vol.67
, pp. 1261-1265
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Pàmies, O.1
Bäckvall, J.E.2
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20
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0035967783
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Lipase/ruthenium-catalyzed dynamic kinetic resolution of hydroxy acids, diols, and hydroxy aldehydes protected with a bulky group
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This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of functionalized alcohols with a sterically bulky group.
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Kim M.J., Choi Y.K., Choi M.Y., Kim M., Park J. Lipase/ruthenium-catalyzed dynamic kinetic resolution of hydroxy acids, diols, and hydroxy aldehydes protected with a bulky group. J Org Chem. 66:2001;4736-4738. This paper describes the use of a ruthenium-catalyzed racemization for the deracemization of functionalized alcohols with a sterically bulky group.
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(2001)
J Org Chem
, vol.66
, pp. 4736-4738
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Kim, M.J.1
Choi, Y.K.2
Choi, M.Y.3
Kim, M.4
Park, J.5
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21
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0035356381
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Dynamic kinetic resolution of β-azido alcohols. An efficient route to chiral aziridines and β-amino alcohols
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Pàmies O., Bäckvall J.E. Dynamic kinetic resolution of β-azido alcohols. An efficient route to chiral aziridines and β-amino alcohols. J Org Chem. 66:2001;4022-4025.
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(2001)
J Org Chem
, vol.66
, pp. 4022-4025
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Pàmies, O.1
Bäckvall, J.E.2
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22
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0346312265
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Efficient lipase-catalyzed kinetic resolution and dynamic kinetic resolution of β-hydroxy nitriles. A route to useful precursors for γ-amino alcohols
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Pàmies O., Bäckvall J.E. Efficient lipase-catalyzed kinetic resolution and dynamic kinetic resolution of β-hydroxy nitriles. A route to useful precursors for γ-amino alcohols. Adv Synth Catal. 343:2001;726-731.
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(2001)
Adv Synth Catal
, vol.343
, pp. 726-731
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Pàmies, O.1
Bäckvall, J.E.2
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23
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0037189176
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An efficient and mild ruthenium-catalyzed racemization of amines: Application to the synthesis of enantiomerically pure amines
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Pàmies O., Ell A.H., Samec J.S.M., Hermanns N., Bäckvall J.E. An efficient and mild ruthenium-catalyzed racemization of amines: application to the synthesis of enantiomerically pure amines. Tetrahedron Lett. 43:2002;4699-4702.
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(2002)
Tetrahedron Lett
, vol.43
, pp. 4699-4702
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Pàmies, O.1
Ell, A.H.2
Samec, J.S.M.3
Hermanns, N.4
Bäckvall, J.E.5
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24
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0000419728
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Dynamic kinetic resolution of acyclic allylic acetates using lipase and palladium
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This work describes the use of a palladium-catalyzed racemization for the deracemization of allylic acetates.
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Choi Y.K., Suh J.H., Lee D., Lim I.T., Jung J.Y., Kim M.J. Dynamic kinetic resolution of acyclic allylic acetates using lipase and palladium. J Org Chem. 64:1999;8423-8424. This work describes the use of a palladium-catalyzed racemization for the deracemization of allylic acetates.
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(1999)
J Org Chem
, vol.64
, pp. 8423-8424
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Choi, Y.K.1
Suh, J.H.2
Lee, D.3
Lim, I.T.4
Jung, J.Y.5
Kim, M.J.6
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25
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0001501091
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Concerted catalytic reactions for conversion of ketones or enol acetates to chiral acetates
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This paper describes the use of a lipase-ruthenium combo for the asymmetric transformation of prochiral substrates, such as ketones and enol acetates.
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Jung H.M., Koh J.H., Kim M.J., Park J. Concerted catalytic reactions for conversion of ketones or enol acetates to chiral acetates. Org Lett. 2:2000;409-411. This paper describes the use of a lipase-ruthenium combo for the asymmetric transformation of prochiral substrates, such as ketones and enol acetates.
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(2000)
Org Lett
, vol.2
, pp. 409-411
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Jung, H.M.1
Koh, J.H.2
Kim, M.J.3
Park, J.4
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26
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0034632398
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Practical ruthenium/lipase-catalyzed asymmetric transformations of ketones and enol acetates to chiral acetates
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This paper describes the use of a lipase-ruthenium combo in the presence of an inexpensive hydrogen source and acyl donor for practical asymmetric transformations.
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Jung H.M., Koh J.H., Kim M.J., Park J. Practical ruthenium/lipase-catalyzed asymmetric transformations of ketones and enol acetates to chiral acetates. Org Lett. 2:2000;2487-2490. This paper describes the use of a lipase-ruthenium combo in the presence of an inexpensive hydrogen source and acyl donor for practical asymmetric transformations.
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(2000)
Org Lett
, vol.2
, pp. 2487-2490
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Jung, H.M.1
Koh, J.H.2
Kim, M.J.3
Park, J.4
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27
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0035856968
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Lipase/palladium-catalyzed asymmetric transformations of ketoximes to optically active amines
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This paper describes the use of a palladium-catalyzed racemization for the deracemization of amines.
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Choi Y.K., Kim M., Ahn Y., Kim M.J. Lipase/palladium-catalyzed asymmetric transformations of ketoximes to optically active amines. Org Lett. 3:2001;4099-4101. This paper describes the use of a palladium-catalyzed racemization for the deracemization of amines.
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(2001)
Org Lett
, vol.3
, pp. 4099-4101
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Choi, Y.K.1
Kim, M.2
Ahn, Y.3
Kim, M.J.4
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