-
5
-
-
44649197822
-
Chiral diphosphine and monodentate phosphorus ligands on a spiro scaffold for transtion-metal-catalyzed asymmetric reactions
-
Xie J H, Zhou Q L. Chiral diphosphine and monodentate phosphorus ligands on a spiro scaffold for transtion-metal-catalyzed asymmetric reactions. Acc Chem Res, 2008, 41: 581-593.
-
(2008)
Acc Chem Res
, vol.41
, pp. 581-593
-
-
Xie, J.H.1
Zhou, Q.L.2
-
6
-
-
58149185277
-
Spiro skeletons: A class of privileged structure for chiral ligand design
-
Ding K, Han Z, Wang Z. Spiro skeletons: A class of privileged structure for chiral ligand design. Chem Asian J, 2009, 4: 32-41.
-
(2009)
Chem Asian J
, vol.4
, pp. 32-41
-
-
Ding, K.1
Han, Z.2
Wang, Z.3
-
7
-
-
0030831034
-
Novel spiro phosphinite ligands and their application in homogeneous catalytic hydrogenation reactions
-
Chan A S C, Hu W H, Pai C C, et al. Novel spiro phosphinite ligands and their application in homogeneous catalytic hydrogenation reactions. J Am Chem Soc, 1997, 119: 9570-9571.
-
(1997)
J Am Chem Soc
, vol.119
, pp. 9570-9571
-
-
Chan, A.S.C.1
Hu, W.H.2
Pai, C.C.3
-
8
-
-
33749828310
-
2-Symmetric chiral bis-(oxazoline) ligands in asymmetric catalysis
-
2-Symmetric chiral bis-(oxazoline) ligands in asymmetric catalysis. Chem Rev, 2006, 106: 3561-3651.
-
(2006)
Chem Rev
, vol.106
, pp. 3561-3651
-
-
Desimoni, G.1
Faita, G.2
Jørgensen, K.A.3
-
9
-
-
0025042702
-
Asymmetric catalytic cyclopropanation of olefins: Bis-oxazoline copper complexes
-
Lowenthal R E, Abiko A, Masamune S. Asymmetric catalytic cyclopropanation of olefins: Bis-oxazoline copper complexes. Tetrahedron Lett, 1990, 31: 6005-6008.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 6005-6008
-
-
Lowenthal, R.E.1
Abiko, A.2
Masamune, S.3
-
10
-
-
84987472013
-
2-Symmetric 4,4′,5,5′-tetrahydrobi(oxazoles) and 4,4′,5,5′-tetrahydro-2,2′-methylenebis (oxazoles) as chiral ligands for enantioselective catalysis preliminary communication
-
2-Symmetric 4, 4′, 5, 5′-tetrahydrobi(oxazoles) and 4, 4′, 5, 5′-tetrahydro-2, 2′-methylenebis (oxazoles) as chiral ligands for enantioselective catalysis preliminary communication. Helv Chim Acta, 1991, 74: 232-240.
-
(1991)
Helv Chim Acta
, vol.74
, pp. 232-240
-
-
Muller, D.1
Umbricht, G.2
Weber, B.3
-
11
-
-
85008090337
-
Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins
-
Evans D A, Woerpel K A, Hinman M M, et al. Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins. J Am Chem Soc, 1991, 113: 726-728.
-
(1991)
J Am Chem Soc
, vol.113
, pp. 726-728
-
-
Evans, D.A.1
Woerpel, K.A.2
Hinman, M.M.3
-
12
-
-
85022460851
-
2-symmetric chiral bis(oxazoline)-iron(III) complex
-
2-symmetric chiral bis(oxazoline)-iron(III) complex. J Am Chem Soc, 1991, 113: 728-729.
-
(1991)
J Am Chem Soc
, vol.113
, pp. 728-729
-
-
Corey, E.J.1
Imai, N.2
Zhang, H.Y.3
-
13
-
-
0028828639
-
The first enantioselective synthesis of the chemotactic factor sirenin by an intramolecular [2+1] cyclization using a new chiral catalyst
-
Gant T G, Noe M C, Corey E J. The first enantioselective synthesis of the chemotactic factor sirenin by an intramolecular [2+1] cyclization using a new chiral catalyst. Tetrahedron Lett, 1995, 36: 8745-8748.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 8745-8748
-
-
Gant, T.G.1
Noe, M.C.2
Corey, E.J.3
-
14
-
-
0029882378
-
Homochiral 2,2′-bis(oxazolyl)-1,1′-binaphthyls as ligands for copper(I)-catalyzed asymmetric cyclopropanation
-
Uozumi Y, Kyota H, Kishi E, et al. Homochiral 2, 2′-bis(oxazolyl)-1, 1′-binaphthyls as ligands for copper(I)-catalyzed asymmetric cyclopropanation. Tetrahedron: Asymmetry, 1996, 7: 1603-1606.
-
(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 1603-1606
-
-
Uozumi, Y.1
Kyota, H.2
Kishi, E.3
-
15
-
-
0029943004
-
A new class of bis-oxazoline ligands for the Cu-catalysed asymmetric cyclopropanation of olefins
-
Bedekar A V, Andersson P G. A new class of bis-oxazoline ligands for the Cu-catalysed asymmetric cyclopropanation of olefins. Tetrahedron Lett, 1996, 37: 4073-4076.
-
(1996)
Tetrahedron Lett
, vol.37
, pp. 4073-4076
-
-
Bedekar, A.V.1
Andersson, P.G.2
-
16
-
-
33645891473
-
Preparation and application of bisoxazoline ligands with a chiral spirobiindane skeleton for asymmetric cyclopropanation and allylic oxidation
-
Liu B, Zhu S F, Wang L X, et al. Preparation and application of bisoxazoline ligands with a chiral spirobiindane skeleton for asymmetric cyclopropanation and allylic oxidation. Tetrahedron: Asymmetry, 2006, 17: 634-641.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 634-641
-
-
Liu, B.1
Zhu, S.F.2
Wang, L.X.3
-
17
-
-
34248531594
-
Highly enantioselective insertion of carbenoids into N-H bonds catalyzed by copper complexes of chiral spiro bisoxazolines
-
Liu B, Zhu S F, Zhang W, et al. Highly enantioselective insertion of carbenoids into N-H bonds catalyzed by copper complexes of chiral spiro bisoxazolines. J Am Chem Soc, 2007, 129: 5834-5835.
-
(2007)
J Am Chem Soc
, vol.129
, pp. 5834-5835
-
-
Liu, B.1
Zhu, S.F.2
Zhang, W.3
-
18
-
-
35548940365
-
Highly enantioselective insertion of carbenoids into O-H bonds of phenols: An efficient approach to chiral α-aryloxycarboxylic esters
-
Chen C, Zhu S F, Liu B, et al. Highly enantioselective insertion of carbenoids into O-H bonds of phenols: An efficient approach to chiral α-aryloxycarboxylic esters. J Am Chem Soc, 2007, 129: 12616-12617.
-
(2007)
J Am Chem Soc
, vol.129
, pp. 12616-12617
-
-
Chen, C.1
Zhu, S.F.2
Liu, B.3
-
19
-
-
38549171363
-
Catalytic asymmetric reaction with water: Enantioselective synthesis of α-hydroxyesters by a coppercarbenoid O-H insertion reaction
-
Zhu S F, Chen C, Cai Y, et al. Catalytic asymmetric reaction with water: Enantioselective synthesis of α-hydroxyesters by a coppercarbenoid O-H insertion reaction. Angew Chem Int Ed, 2008, 47: 932-934.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 932-934
-
-
Zhu, S.F.1
Chen, C.2
Cai, Y.3
-
20
-
-
70349904295
-
Spiro[4,4]-1,6-nonadiene-based phosphine-oxazoline ligands for iridium-catalyzed enantioselective hydrogenation of ketimines
-
Han Z, Wang Z, Zhang X, et al. Spiro[4, 4]-1, 6-nonadiene-based phosphine-oxazoline ligands for iridium-catalyzed enantioselective hydrogenation of ketimines. Angew Chem Int Ed, 2009, 48: 5345-5349.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 5345-5349
-
-
Han, Z.1
Wang, Z.2
Zhang, X.3
-
21
-
-
72149116472
-
Highly enantioselective hydrogenation of α-aryl-β-substituted acrylic acids catalyzed by Ir-SpinPHOX
-
Zhang Y, Han Z B, Li F Y, et al. Highly enantioselective hydrogenation of α-aryl-β-substituted acrylic acids catalyzed by Ir-SpinPHOX. Chem Commun, 2010, 46: 156-158.
-
(2010)
Chem Commun
, vol.46
, pp. 156-158
-
-
Zhang, Y.1
Han, Z.B.2
Li, F.Y.3
-
22
-
-
0032836899
-
An efficient synthesis and resolution of (+/-)-cis, cis-spiro[4,4]nonane-1,6-diol
-
Nieman J A, Keay B A. An efficient synthesis and resolution of (+/-)-cis, cis-spiro[4, 4]nonane-1, 6-diol. Synth Commun, 1999, 29: 3829-3840.
-
(1999)
Synth Commun
, vol.29
, pp. 3829-3840
-
-
Nieman, J.A.1
Keay, B.A.2
-
23
-
-
19344376676
-
Stereoselective preparation of spirane bridged, sandwiched bisarenes
-
Rolandsgard M, Baldawi S, Sirbu D, et al. Stereoselective preparation of spirane bridged, sandwiched bisarenes. Tetrahedron, 2005, 61: 4129-4140.
-
(2005)
Tetrahedron
, vol.61
, pp. 4129-4140
-
-
Rolandsgard, M.1
Baldawi, S.2
Sirbu, D.3
-
24
-
-
0037140757
-
Synthesis of cis-fused hexahydro-4aH-indeno[1,2-b]pyridines via intramolecular Ritter reaction and their conversion into tricyclic analogues of NK-1 and dopamine receptor ligands
-
van Emelen K, De Wit T, Hoornaert G J, et al. Synthesis of cis-fused hexahydro-4aH-indeno[1, 2-b]pyridines via intramolecular Ritter reaction and their conversion into tricyclic analogues of NK-1 and dopamine receptor ligands. Tetrahedron, 2002, 58: 4225-4236.
-
(2002)
Tetrahedron
, vol.58
, pp. 4225-4236
-
-
van Emelen, K.1
de Wit, T.2
Hoornaert, G.J.3
-
26
-
-
2942702061
-
-
Ibrahim H, Togni A. Enantioselective halogenation reactions. Chem Commun, 2004, 1147-1155.
-
-
-
-
27
-
-
14344261164
-
-
France S, Weatherwax A, Lectka T. Recent developments in cata lytic, asymmetric α-halogenation: A new frontier in asymmetric catalysis. Eur J Org Chem, 2005, 475-479.
-
-
-
-
28
-
-
18044378817
-
Strategies for catalytic asymmetric electrophilic α halogenation of carbonyl compounds
-
Oestreich M. Strategies for catalytic asymmetric electrophilic α halogenation of carbonyl compounds. Angew Chem Int Ed, 2005, 44: 2324-2327.
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 2324-2327
-
-
Oestreich, M.1
-
29
-
-
25844477921
-
Organocatalytic asymmetric α-halogenation of 1,3-dicarbonyl compounds
-
Bartoli G, Bosco M, Carlone A, et al. Organocatalytic asymmetric α-halogenation of 1, 3-dicarbonyl compounds. Angew Chem Int Ed, 2005, 44: 6219-6222.
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 6219-6222
-
-
Bartoli, G.1
Bosco, M.2
Carlone, A.3
-
30
-
-
70349904562
-
Enantioselective linchpin catalysis by SOMO catalysis: An approach to the asymmetric α-chlorination of aldehydes and terminal epoxide formation
-
Amatore M, Beeson T D, Brown S P. Enantioselective linchpin catalysis by SOMO catalysis: An approach to the asymmetric α-chlorination of aldehydes and terminal epoxide formation. Angew Chem Int Ed, 2009, 48: 5121-5124.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 5121-5124
-
-
Amatore, M.1
Beeson, T.D.2
Brown, S.P.3
-
31
-
-
2442584755
-
Catalytic asymmetric bromination and chlorination of β-ketoesters
-
Marigo M, Kumaragurubaran N, Jørgensen K A. Catalytic asymmetric bromination and chlorination of β-ketoesters. Chem Eur J, 2004, 10: 2133-2137.
-
(2004)
Chem Eur J
, vol.10
, pp. 2133-2137
-
-
Marigo, M.1
Kumaragurubaran, N.2
Jørgensen, K.A.3
-
32
-
-
22144453934
-
Highly enantioselective catalytic fluorination and chlorination reactions of carbonyl compounds capable of two-point binding
-
Shibata N, Kohno J, Takai K, et al. Highly enantioselective catalytic fluorination and chlorination reactions of carbonyl compounds capable of two-point binding. Angew Chem Int Ed, 2005, 44: 4204-4207.
-
(2005)
Angew Chem Int Ed
, vol.44
, pp. 4204-4207
-
-
Shibata, N.1
Kohno, J.2
Takai, K.3
-
33
-
-
37549054653
-
Desymmetrization-like catalytic enantioselective fluorination of malonates and its application to pharmaceutically attractive molecules
-
Reddy D S, Shibata N, Nagai J, et al. Desymmetrization-like catalytic enantioselective fluorination of malonates and its application to pharmaceutically attractive molecules. Angew Chem Int Ed, 2008, 47: 164-168.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 164-168
-
-
Reddy, D.S.1
Shibata, N.2
Nagai, J.3
|