-
1
-
-
79952679097
-
Phosphinephosphinite and phosphine-phosphite ligands preparation and applications in asymmetric catalysis
-
Fernandez-Perez, H.; Etayo, P.; Panossian, A.; Vidal-Ferran, A.; Phosphinephosphinite and phosphine-phosphite ligands: preparation and applications in asymmetric catalysis. Chem. Rev., 2011, 111, 2119-2176.
-
(2011)
Chem. Rev.
, vol.111
, pp. 2119-2176
-
-
Fernandez-Perez, H.1
Etayo, P.2
Panossian, A.3
Vidal-Ferran, A.4
-
5
-
-
21244479264
-
A highly efficient organocatalyst for direct aldol reactions of ketones with aldedydes
-
Tang, Z.; Yang, Z. H.; Chen, X. H.; Cun, L. F.; Gong, L. Z. A highly efficient organocatalyst for direct aldol reactions of ketones with aldedydes. J. Am. Chem. Soc., 2005, 127, 9285-9289.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 9285-9289
-
-
Tang, Z.1
Yang, Z.H.2
Chen, X.H.3
Cun, L.F.4
Gong, L.Z.5
-
6
-
-
80051592008
-
Palladium-catalyzed asymmetric allylic alkylations of polynitrogen-containing aromatic heterocycles
-
Trost, B. M.; Thaisrivongs, D. A. Hartwig, J. Palladium-catalyzed asymmetric allylic alkylations of polynitrogen-containing aromatic heterocycles. J. Am. Chem. Soc., 2011, 133, 12439-12441.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 12439-12441
-
-
Trost, B.M.1
Thaisrivongs, D.A.2
Hartwig, J.3
-
7
-
-
0034823238
-
Highly regio-and enantio-selective Pd-catalyzed allylic alkylation and amination of monosubstituted allylic acetates with novel ferrocene P, N-ligands
-
You, S. L.; Zhu, X. Z.; Luo, Y. M.; Hou, X. L.; Dai, L. X. Highly regio-and enantio-selective Pd-catalyzed allylic alkylation and amination of monosubstituted allylic acetates with novel ferrocene P, N-ligands. J. Am. Chem. Soc., 2001, 123, 7471-7472.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7471-7472
-
-
You, S.L.1
Zhu, X.Z.2
Luo, Y.M.3
Hou, X.L.4
Dai, L.X.5
-
8
-
-
0037067033
-
Mechanism of asymmetric hydrogenation of α-(Acylamino)acrylic esters catalyzed by BINAP-Ruthenium(II) diacetate
-
Kitamura, M.; Tsukamoto, M.; Bessho, Y.; Yoshimura, M.; Kobs, U; Widhalm, M.; Noyori, R. Mechanism of asymmetric hydrogenation of α-(Acylamino)acrylic esters catalyzed by BINAP-Ruthenium(II) diacetate. J. Am. Chem. Soc., 2002, 124, 6649-6667
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 6649-6667
-
-
Kitamura, M.1
Tsukamoto, M.2
Bessho, Y.3
Yoshimura, M.4
Kobs, U.5
Widhalm, M.6
Noyori, R.7
-
9
-
-
83755171357
-
Catalytic asymmetric synthesis of stable oxetenes via lewis acid-promoted [2 + 2] cycloaddition
-
Aikawa, K.; Hioki, Y.; Shimizu, N.; Mikami, K. Catalytic asymmetric synthesis of stable oxetenes via lewis acid-promoted [2 + 2] cycloaddition. J. Am. Chem. Soc., 2011, 133, 20092-20095.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 20092-20095
-
-
Aikawa, K.1
Hioki, Y.2
Shimizu, N.3
Mikami, K.4
-
10
-
-
0030831034
-
Novel spiro phosphinite ligands and their application in homogeneous catalytic hydrogenation reactions
-
Chan, A. S. C.; Hu, W. H.; Pai, C. C.; Lau, C. P.; Jiang, Y. Z.; Mi, A. Q.; Yan, M.; Sun, J.; Lou, R. L.; Deng, J. G. 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
Lau, C.P.4
Jiang, Y.Z.5
Mi, A.Q.6
Yan, M.7
Sun, J.8
Lou, R.L.9
Deng, J.G.10
-
11
-
-
79952684475
-
Transition metal-catalyzed enantioselective hydrogenation of enamines and imines
-
Xie, J. H.; Zhu, S. F.; Zhou, Q. L. Transition metal-catalyzed enantioselective hydrogenation of enamines and imines. Chem. Rev., 2011, 111, 1713-1760.
-
(2011)
Chem. Rev.
, vol.111
, pp. 1713-1760
-
-
Xie, J.H.1
Zhu, S.F.2
Zhou, Q.L.3
-
12
-
-
80051716582
-
Asymmetric organocatalytic cyclization and cycloadd ition reactions
-
Moyano, A.; Rios, R. Asymmetric organocatalytic cyclization and cycloadd ition reactions Chem. Rev., 2011, 111, 4703-4832.
-
(2011)
Chem. Rev.
, vol.111
, pp. 4703-4832
-
-
Moyano, A.1
Rios, R.2
-
13
-
-
4143136647
-
Asymmetric Organic Catalysis with Modified Cinchona Alkaloids
-
Tian, S. K.; Chen, Y. G.; Hang, J. F.; Tang, L.; McDaid, P.; Deng, L. Asymmetric Organic Catalysis with Modified Cinchona Alkaloids. Acc. Chem. Res., 2004, 37, 621-631
-
(2004)
Acc. Chem. Res.
, vol.37
, pp. 621-631
-
-
Tian, S.K.1
Chen, Y.G.2
Hang, J.F.3
Tang, L.4
McDaid, P.5
Deng, L.6
-
14
-
-
4344684124
-
Ligands derived from carbohydrates for asymmetric catalysis
-
Dieguez, M.; Pamies, O.; Claver, C. Ligands derived from carbohydrates for asymmetric catalysis. Chem. Rev., 2004, 104, 3189-3215.
-
(2004)
Chem. Rev.
, vol.104
, pp. 3189-3215
-
-
Dieguez, M.1
Pamies, O.2
Claver, C.3
-
15
-
-
65349163537
-
Diasteroselective alkynylation of glucosemodified imines with terminal alkynes
-
Mao, J. G.; Zhang, P. F. Diasteroselective alkynylation of glucosemodified imines with terminal alkynes. Tetrahedron: Asymmetry 2009, 20, 566-569
-
(2009)
Tetrahedron: Asymmetry
, vol.20
, pp. 566-569
-
-
Mao, J.G.1
Zhang, P.F.2
-
16
-
-
78650312173
-
A novel 1-glycosyl-1Htriazole-based P, N ligand for Rhodium-catalyzed asymmetric hydrosilylation of ketones
-
Shen, C.; Zhang, P. F.; Chen, X. Z. A novel 1-glycosyl-1Htriazole-based P, N ligand for Rhodium-catalyzed asymmetric hydrosilylation of ketones. Helv. Chim. Acta., 2010, 93, 2433-2438.
-
(2010)
Helv. Chim. Acta.
, vol.93
, pp. 2433-2438
-
-
Shen, C.1
Zhang, P.F.2
Chen, X.Z.3
-
17
-
-
72149105052
-
Carbohydrates as building blocks of privileged ligands
-
Benessere, V.; Litto, R. D.; Roma, A. D.; Ruffo, F. Carbohydrates as building blocks of privileged ligands. Coord. Chem. Rev., 2010, 254, 390-401.
-
(2010)
Coord. Chem. Rev.
, vol.254
, pp. 390-401
-
-
Benessere, V.1
Litto, R.D.2
Roma, A.D.3
Ruffo, F.4
-
18
-
-
77954383638
-
Use of sugar-based ligands in selective catalysis: Recent developments
-
Woodward, S.; Diéguez, M.; Pàmies, O. Use of sugar-based ligands in selective catalysis: Recent developments. Coord. Chem. Rev., 2010, 254, 2007-2030.
-
(2010)
Coord. Chem. Rev.
, vol.254
, pp. 2007-2030
-
-
Woodward, S.1
Diéguez, M.2
Pàmies, O.3
-
19
-
-
33744830047
-
Assembly state of catalytic modules as chiral switches in asymmetric Strecker amino acid synthesis
-
Kato, N.; Mita, T.; Kanai, M.; Therrien, B.; Kawano, M.; Yamaguchi, K.; Danjo, H.; Sei, Y.; Sato, A.; Furusho, S.; Shibasaki, M. Assembly state of catalytic modules as chiral switches in asymmetric Strecker amino acid synthesis. J. Am. Chem. Soc., 2006, 128, 6768-6769
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 6768-6769
-
-
Kato, N.1
Mita, T.2
Kanai, M.3
Therrien, B.4
Kawano, M.5
Yamaguchi, K.6
Danjo, H.7
Sei, Y.8
Sato, A.9
Furusho, S.10
Shibasaki, M.11
-
20
-
-
33746275938
-
Regio-and enantioselective epoxidation of dienes by a chiral dioxirane: Synthesis of optically active vinyl cis-Epoxides
-
Burke, C. P.; Shi, Y. Regio-and enantioselective epoxidation of dienes by a chiral dioxirane: synthesis of optically active vinyl cis-Epoxides. Angew. Chem. Int. Ed., 2006, 45, 4475-4478.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 4475-4478
-
-
Burke, C.P.1
Shi, Y.2
-
21
-
-
35748983854
-
Carbohydrates as synthetic tools in organic chemistry
-
Boysen, M. M. K. Carbohydrates as synthetic tools in organic chemistry. Chem. Eur. J., 2007, 13, 8648-8659.
-
(2007)
Chem. Eur. J.
, vol.13
, pp. 8648-8659
-
-
Boysen, M.M.K.1
-
22
-
-
9644267855
-
Electronic amplification of selectivity in Rh-catalyzed hydrogenations: D-glucose-derived ligands for the synthesis of D-or L-Amino Acids
-
RajanBabu, T. V.; Ayers, T. A.; Casalnuovo, A. L. Electronic amplification of selectivity in Rh-catalyzed hydrogenations: D-glucose-derived ligands for the synthesis of D-or L-Amino Acids. J. Am. Chem. Soc., 1994, 116, 4101-4102
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 4101-4102
-
-
RajanBabu, T.V.1
Ayers, T.A.2
Casalnuovo, A.L.3
-
23
-
-
0001486820
-
Carbohydrate phosphinites as practical ligands in asymmetric catalysis: Electronic effects and dependence of backbone chirality in Rhcatalyzed asymmetric hydrogenations. synthesis of R-or S-amino acids using natural sugars as ligand precursors
-
RajanBabu, T. V.; Ayers, T. A.; Halliday, G. A.; You, K. K.; Calabrese, J. C. Carbohydrate phosphinites as practical ligands in asymmetric catalysis: electronic effects and dependence of backbone chirality in Rhcatalyzed asymmetric hydrogenations. synthesis of R-or S-amino acids using natural sugars as ligand precursors J. Org. Chem., 1997, 62, 6012-6028.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6012-6028
-
-
RajanBabu, T.V.1
Ayers, T.A.2
Halliday, G.A.3
You, K.K.4
Calabrese, J.C.5
-
24
-
-
84857559636
-
Pd-and Mo-Catalyzed asymmetric allylic alkylation
-
Trost, B. M. Pd-and Mo-Catalyzed asymmetric allylic alkylation. Org. Process Res. Dev., 2012, 16, 185-194.
-
(2012)
Org. Process Res. Dev.
, vol.16
, pp. 185-194
-
-
Trost, B.M.1
-
25
-
-
33748791737
-
Bis(phosphinoamides) based on sugars for highly enantioselective allylic substitution: Inversion of stereocontrol by switching from glucose to mannose
-
Ruffo, F.; Litto, R. D.; Roma, A. D.; D'Errico, A.; Magnolia, S. Bis(phosphinoamides) based on sugars for highly enantioselective allylic substitution: inversion of stereocontrol by switching from glucose to mannose. Tetrahedron: Asymmetry 2006, 17, 2265-2269.
-
(2006)
Tetrahedron: Asymmetry
, vol.17
, pp. 2265-2269
-
-
Ruffo, F.1
Litto, R.D.2
Roma, A.D.3
D'Errico, A.4
Magnolia, S.5
-
26
-
-
55349105375
-
Carbohydrates as building blocks of privileged ligands for multiphasic asymmetric catalysis
-
Benessere, V.; Roma, A. D.; Ruffo, F. Carbohydrates as building blocks of privileged ligands for multiphasic asymmetric catalysis. ChemSusChem 2008, 1, 425-430.
-
(2008)
ChemSusChem
, vol.1
, pp. 425-430
-
-
Benessere, V.1
Roma, A.D.2
Ruffo, F.3
-
27
-
-
80053948781
-
New tagged naplephos ligands for asymmetric allylic substitutions under traditional and unconventional conditions
-
Benessere, V.; Lega, M.; Silipo, A.; Ruffo, F. New tagged naplephos ligands for asymmetric allylic substitutions under traditional and unconventional conditions. Tetrahedron 2011, 67, 4826-4831.
-
(2011)
Tetrahedron
, vol.67
, pp. 4826-4831
-
-
Benessere, V.1
Lega, M.2
Silipo, A.3
Ruffo, F.4
-
28
-
-
55349099483
-
Amino-sugar modular ligands-useful cores for the formation of asymmetric copper 1,4-addition catalysts
-
Roma, A. D.; Ruffo, F.; Woodward, S. Amino-sugar modular ligands-useful cores for the formation of asymmetric copper 1,4-addition catalysts. Chem. Commun., 2008, 5384-5386.
-
(2008)
Chem. Commun.
, pp. 5384-5386
-
-
Roma, A.D.1
Ruffo, F.2
Woodward, S.3
-
29
-
-
0002685803
-
Enantioselective allylic substitution using a novel (phosphino-α-D-glucopyrano-oxazo-line)palladium catalyst
-
Gläser, B.; Kunz, H. Enantioselective allylic substitution using a novel (phosphino-α-D-glucopyrano-oxazo-line)palladium catalyst. Synlett 1998, 53-54.
-
(1998)
Synlett
, pp. 53-54
-
-
Gläser, B.1
Kunz, H.2
-
30
-
-
0033531439
-
Palladiumcatalyzed asymmetric allylic alkylation using new chiral phosphinite-nitrogen ligands derived from D-Glucosamine
-
Yonehara, K.; Hashizume, T.; Mori, K.; Ohe, K.; Uemura, S. Palladiumcatalyzed asymmetric allylic alkylation using new chiral phosphinite-nitrogen ligands derived from D-Glucosamine. Chem. Commun., 1999, 415-416
-
(1999)
Chem. Commun.
, pp. 415-416
-
-
Yonehara, K.1
Hashizume, T.2
Mori, K.3
Ohe, K.4
Uemura, S.5
-
31
-
-
0033601268
-
Palladiumcatalyzed asymmetric allylic substitution reactions using new chiral phosphinite-oxazoline ligands derived from D-Glucosamine
-
Yonehara, K.; Hashizume, T.; Mori, K.; Ohe, K.; Uemura, S. Palladiumcatalyzed asymmetric allylic substitution reactions using new chiral phosphinite-oxazoline ligands derived from D-Glucosamine J. Org. Chem., 1999, 64, 9374-9380.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 9374-9380
-
-
Yonehara, K.1
Hashizume, T.2
Mori, K.3
Ohe, K.4
Uemura, S.5
-
32
-
-
0034714496
-
A novel amphiphilic chiral ligand derived from D-Glucosamine. Application to palladiumcatalyzed asymmetric allylic substitution reaction in an aqueous or an organic medium, allowing for catalyst recycling
-
Hashizume, T.; Yonehara, K.; Ohe, K.; Uemura, S. A novel amphiphilic chiral ligand derived from D-Glucosamine. Application to palladiumcatalyzed asymmetric allylic substitution reaction in an aqueous or an organic medium, allowing for catalyst recycling. J. Org. Chem., 2000, 65, 5197-5201
-
(2000)
J. Org. Chem.
, vol.65
, pp. 5197-5201
-
-
Hashizume, T.1
Yonehara, K.2
Ohe, K.3
Uemura, S.4
-
33
-
-
0003002302
-
Palladium-catalyzed asymmetric intermolecular arylation of cyclic or acyclic alkenes using phosphinite-oxazoline ligands derived form Dglucosamine
-
Yonehara, K.; Mori, K.; Hashizume, T.; Chung, K. G.; Ohe, K.; Uemura, S. Palladium-catalyzed asymmetric intermolecular arylation of cyclic or acyclic alkenes using phosphinite-oxazoline ligands derived form Dglucosamine. J. Organomet. Chem., 2000, 603, 40-49.
-
(2000)
J. Organomet. Chem.
, vol.603
, pp. 40-49
-
-
Yonehara, K.1
Mori, K.2
Hashizume, T.3
Chung, K.G.4
Ohe, K.5
Uemura, S.6
-
34
-
-
29144447770
-
Modular furanoside diphosphite ligands for Pd-Catalyzed asymmetric allylic substitution reactions: Scope and limitations
-
Mata, Y.; Diéguez, M.; Pàmies, O.; Claver, C. Modular furanoside diphosphite ligands for Pd-Catalyzed asymmetric allylic substitution reactions: scope and limitations. Adv. Synth. Catal., 2005, 347, 1943-1947.
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1943-1947
-
-
Mata, Y.1
Diéguez, M.2
Pàmies, O.3
Claver, C.4
-
35
-
-
44949222632
-
Chiral pyranoside phosphite-oxazolines: A new class of ligand for asymmetric catalytic hydrogenation of 1lkenes
-
Dieguez, M.; Mazuela, J.; Pamies, O.; Verendel, J. J.; Andersson, P. G. Chiral pyranoside phosphite-oxazolines: a new class of ligand for asymmetric catalytic hydrogenation of 1lkenes. J. Am. Chem. Soc., 2008, 130, 7208-7209.
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7208-7209
-
-
Dieguez, M.1
Mazuela, J.2
Pamies, O.3
Verendel, J.J.4
Andersson, P.G.5
-
36
-
-
80052098490
-
Pyranoside phosphite_oxazoline ligands for the highly versatile and enantioselective Ir-catalyzed hydrogenation of minimally functionalized olefins. A combined theoretical and experimental study
-
Mazuela, J.; Norrby, P. O.; Andersson, P. G.; Pamies, O.; Dieguez, M. Pyranoside phosphite_oxazoline ligands for the highly versatile and enantioselective Ir-catalyzed hydrogenation of minimally functionalized olefins. A combined theoretical and experimental study. J. Am. Chem. Soc., 2011, 133, 13634-13645.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 13634-13645
-
-
Mazuela, J.1
Norrby, P.O.2
Andersson, P.G.3
Pamies, O.4
Dieguez, M.5
-
37
-
-
0037028566
-
Tunable ligands for asymmetric catalysis: Readily available carbohydrate-derived diarylphosphinites induce high selectivity in the hydrovinylation of styrene derivatives
-
Park. H.; RajanBabu, T. V. Tunable ligands for asymmetric catalysis: readily available carbohydrate-derived diarylphosphinites induce high selectivity in the hydrovinylation of styrene derivatives. J. Am. Chem. Soc., 2002, 124, 734-735.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 734-735
-
-
Park, H.1
RajanBabu, T.V.2
-
38
-
-
20444481391
-
Tunable phosphinite, phosphite and phosphoramidite ligands for the asymmetric hydrovinylation reactions
-
Park, H.; Kumareswaran, R.; RajanBabu, T. V. Tunable phosphinite, phosphite and phosphoramidite ligands for the asymmetric hydrovinylation reactions Tetrahedron 2005, 61, 6352-6367.
-
(2005)
Tetrahedron
, vol.61
, pp. 6352-6367
-
-
Park, H.1
Kumareswaran, R.2
RajanBabu, T.V.3
-
39
-
-
26444565731
-
Influence on the enantioselectivity in allylic alkylation of the spacer between the amido group of Dglucosamine and the diphenylphosphino group
-
Konovets, A.; Glegola, K.; Penciu, A.; Framery, E.; Jubault, P.; Goux-Henry, C.; Pietrusiewicz, K. M.; Quirion, J. C.; Sinou, D. Influence on the enantioselectivity in allylic alkylation of the spacer between the amido group of Dglucosamine and the diphenylphosphino group. Tetrahedron: Asymmetry 2005, 16, 3183-3187.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 3183-3187
-
-
Konovets, A.1
Glegola, K.2
Penciu, A.3
Framery, E.4
Jubault, P.5
Goux-Henry, C.6
Pietrusiewicz, K.M.7
Quirion, J.C.8
Sinou, D.9
-
40
-
-
0142227153
-
Palladium-catalyzed asymmetric allylic alkylation using chiral glucosamine-based monophosphines
-
Tollabi, M.; Framery, E.; Goux-Henry, C.; Sinou, D. Palladium-catalyzed asymmetric allylic alkylation using chiral glucosamine-based monophosphines Tetrahedron: Asymmetry 2003, 14, 3329-3333
-
(2003)
Tetrahedron: Asymmetry
, vol.14
, pp. 3329-3333
-
-
Tollabi, M.1
Framery, E.2
Goux-Henry, C.3
Sinou, D.4
-
41
-
-
34249983608
-
Influence on the enantioselectivity in allylic alkylation of the anomeric position of the phosphine-amide ligands derived from D-glucosamine
-
Glego, K.; Framery, E.; Goux-Henry, C.; Pietrusiewicz, K. M.; Sinou, D. Influence on the enantioselectivity in allylic alkylation of the anomeric position of the phosphine-amide ligands derived from D-glucosamine. Tetrahedron 2007, 63, 7133-7141.
-
(2007)
Tetrahedron
, vol.63
, pp. 7133-7141
-
-
Glego, K.1
Framery, E.2
Goux-Henry, C.3
Pietrusiewicz, K.M.4
Sinou, D.5
-
42
-
-
53349164210
-
Simple D-glucosamine-based phosphine-imine and phosphineamine ligands in Pd-catalyzed asymmetric allylic alkylations
-
Glegoa, K.; Johannesen, S. A.; Thim, L.; Goux-Henry, C. Skrydstrup, T.; Framery, E. Simple D-glucosamine-based phosphine-imine and phosphineamine ligands in Pd-catalyzed asymmetric allylic alkylations. Tetrahedron Lett., 2008, 49, 6635-6638.
-
(2008)
Tetrahedron Lett.
, vol.49
, pp. 6635-6638
-
-
Glegoa, K.1
Johannesen, S.A.2
Thim, L.3
Goux-Henry, C.4
Skrydstrup, T.5
Framery, E.6
-
43
-
-
77957552439
-
Synthesis of novel carbohydrate-based iminophosphinite ligands in Pd-catalyzed asymmetric allylic alkylations
-
Shen, C.; Xia, H. J.; Zheng, H.; Zhang, P. F.; Chen, X. Z. Synthesis of novel carbohydrate-based iminophosphinite ligands in Pd-catalyzed asymmetric allylic alkylations. Tetrahedron: Asymmetry 2010, 21, 1936-1941.
-
(2010)
Tetrahedron: Asymmetry
, vol.21
, pp. 1936-1941
-
-
Shen, C.1
Xia, H.J.2
Zheng, H.3
Zhang, P.F.4
Chen, X.Z.5
-
44
-
-
80054707877
-
Synthesis of novel carbohydrate-based chiral P, N ligands and their applications in Cu-catalyzed enantioselective 1,4-conjugate additions
-
Xia, H. J.; Yan, H.; Shen, C.; Shen, F. Y.; Zhang, P. F. Synthesis of novel carbohydrate-based chiral P, N ligands and their applications in Cu-catalyzed enantioselective 1,4-conjugate additions. Catal. Commun., 2011, 16, 155-158.
-
(2011)
Catal. Commun.
, vol.16
, pp. 155-158
-
-
Xia, H.J.1
Yan, H.2
Shen, C.3
Shen, F.Y.4
Zhang, P.F.5
-
45
-
-
33845749263
-
glucoBox-a new carbohydrate-based bis(oxazoline) ligand. Synthesis and first application
-
Irmak, M.; Groschner, A.; Boysen, M. M. K. glucoBox-a new carbohydrate-based bis(oxazoline) ligand. Synthesis and first application. Chem. Commun., 2007, 177-179
-
(2007)
Chem. Commun.
, pp. 177-179
-
-
Irmak, M.1
Groschner, A.2
Boysen, M.M.K.3
-
46
-
-
34848926829
-
First synthesis of a carbohydrate-derived pyridyl bis(thiazoline) ligand
-
Irmak, M.; Groschner, A.; Boysen, M. M. K. First synthesis of a carbohydrate-derived pyridyl bis(thiazoline) ligand. Tetrahedron Lett., 2007, 48, 7890-7893.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 7890-7893
-
-
Irmak, M.1
Groschner, A.2
Boysen, M.M.K.3
-
47
-
-
46649102695
-
A new pyridyl bis(oxazoline) ligand prepared from D-glucosamine for asymmetric alkynylation of imines
-
Irmak, M.; Boysen, M. M. K. A new pyridyl bis(oxazoline) ligand prepared from D-glucosamine for asymmetric alkynylation of imines. Adv. Synth. Catal., 2008, 350, 403-405.
-
(2008)
Adv. Synth. Catal.
, vol.350
, pp. 403-405
-
-
Irmak, M.1
Boysen, M.M.K.2
-
48
-
-
61849118917
-
Sweets for catalysis-facile optimization of carbohydrate-based bis(oxazoline) ligands
-
Minuth, T.; Irmak, M.; Groschner, A.; Lehnert, T.; Boysen, M. M. K. Sweets for catalysis-facile optimization of carbohydrate-based bis(oxazoline) ligands. Eur. J. Org. Chem., 2009, 997-1008
-
(2009)
Eur. J. Org. Chem.
, pp. 997-1008
-
-
Minuth, T.1
Irmak, M.2
Groschner, A.3
Lehnert, T.4
Boysen, M.M.K.5
-
49
-
-
77951006657
-
Bis(oxazolines) based on glycopyranosides-steric, configurational and conformational influences on stereoselectivity
-
doi:10.3762/bjoc.6.23
-
Minuth, T.; Boysen, M. M. K. Bis(oxazolines) based on glycopyranosides-steric, configurational and conformational influences on stereoselectivity. Beilstein J. Org. Chem., 2010, 6, 23; doi:10.3762/bjoc.6.23.
-
(2010)
Beilstein J. Org. Chem.
, vol.6
, pp. 23
-
-
Minuth, T.1
Boysen, M.M.K.2
-
50
-
-
0035965115
-
Novel chiral diimines and diamines derived from sugars in copper-catalysed asymmetric cyclopropanation
-
Borriello, C.; Cucciolito, M. E.; Panunzi, A.; Ruffo, F. Novel chiral diimines and diamines derived from sugars in copper-catalysed asymmetric cyclopropanation. Tetrahedron: Asymmetry 2001, 12, 2467-2471.
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 2467-2471
-
-
Borriello, C.1
Cucciolito, M.E.2
Panunzi, A.3
Ruffo, F.4
-
51
-
-
1042298823
-
Mn(III) complexes of chiral 'salen' type ligands derived from carbohydrates in the asymmetric epoxidation of styrenes
-
Borriello, C.; Litto, R. D.; Panunzi, A.; Ruffo, F. Mn(III) complexes of chiral 'salen' type ligands derived from carbohydrates in the asymmetric epoxidation of styrenes. Tetrahedron: Asymmetry 2004, 15, 681-686.
-
(2004)
Tetrahedron: Asymmetry
, vol.15
, pp. 681-686
-
-
Borriello, C.1
Litto, R.D.2
Panunzi, A.3
Ruffo, F.4
-
52
-
-
63449116735
-
Carbohydrate-based pyridine-2-carboxamides for Mo-catalyzed asymmetric allylic alkylations
-
Benessere, V.; Litto, R. D.; Ruffo, F.; Moberg, C. Carbohydrate-based pyridine-2-carboxamides for Mo-catalyzed asymmetric allylic alkylations. Eur. J. Org. Chem., 2009, 1352-1356.
-
(2009)
Eur. J. Org. Chem.
, pp. 1352-1356
-
-
Benessere, V.1
Litto, R.D.2
Ruffo, F.3
Moberg, C.4
-
53
-
-
0037070072
-
Highly enantioselective diethylzinc addition to aldehydes catalyzed by D-glucosamine derivatives
-
Bauer, T.; Tarasiuk, J.; Pasniczek, K. Highly enantioselective diethylzinc addition to aldehydes catalyzed by D-glucosamine derivatives. Tetrahedron: Asymmetry 2002, 13, 77-82.
-
(2002)
Tetrahedron: Asymmetry
, vol.13
, pp. 77-82
-
-
Bauer, T.1
Tarasiuk, J.2
Pasniczek, K.3
-
54
-
-
21844449153
-
O, N, O'-tridentate ligands derived from carbohydrates in the V(IV)-promoted asymmetric oxidation of thioanisole
-
Cucciolito, E. M.; Litto, R. D.; Roviello, G.; Ruffo, F. O, N, O'-tridentate ligands derived from carbohydrates in the V(IV)-promoted asymmetric oxidation of thioanisole. Journal of Molecular Catalysis A: Chemical. 2005, 23, 6 176-181.
-
(2005)
Journal of Molecular Catalysis A: Chemical.
, vol.23
, Issue.6
, pp. 176-181
-
-
Cucciolito, E.M.1
Litto, R.D.2
Roviello, G.3
Ruffo, F.4
-
55
-
-
12344249542
-
Carbohydrate-derived aminoalcohol ligands for asymmetric Reformatsky reactions
-
Emmerson, D. P. G.; Hems, W. P.; Davis, B. G. Carbohydrate-derived aminoalcohol ligands for asymmetric Reformatsky reactions. Tetrahedron: Asymmetry 2005, 16, 213-221.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 213-221
-
-
Emmerson, D.P.G.1
Hems, W.P.2
Davis, B.G.3
-
56
-
-
31544459847
-
Carbohydrate-derived amino-alcohol ligands for asymmetric alkynylation of aldehydes
-
Emmerson, D. P. G.; Hems, W. P.; Davis, B. G. Carbohydrate-derived amino-alcohol ligands for asymmetric alkynylation of aldehydes. Org. Lett., 2006, 8, 207-210
-
(2006)
Org. Lett.
, vol.8
, pp. 207-210
-
-
Emmerson, D.P.G.1
Hems, W.P.2
Davis, B.G.3
-
57
-
-
0344981491
-
Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: Dialkylzinc-aldehyde additions
-
Emmerson, D. P. G.; Villard, R.; Mugnaini, C.; Batsanov, A.; Howard, J. A. K.; Hems, W. P.; Tooze, R. P.; Davis, B. G. Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions. Org. Biomol. Chem., 2003, 1, 3826-3838.
-
(2003)
Org. Biomol. Chem.
, vol.1
, pp. 3826-3838
-
-
Emmerson, D.P.G.1
Villard, R.2
Mugnaini, C.3
Batsanov, A.4
Howard, J.A.K.5
Hems, W.P.6
Tooze, R.P.7
Davis, B.G.8
-
58
-
-
33646707261
-
Mixed S/N and S/P/N ligands from carbohydrates: Synthesis and application in palladium-catalyzed allylic alkylation
-
Khiar, N.; Suarez, B.; Fernandez, I. Mixed S/N and S/P/N ligands from carbohydrates: synthesis and application in palladium-catalyzed allylic alkylation Inorg. Chim. Acta., 2006, 359, 3048-3053.
-
(2006)
Inorg. Chim. Acta.
, vol.359
, pp. 3048-3053
-
-
Khiar, N.1
Suarez, B.2
Fernandez, I.3
-
59
-
-
34547229120
-
Enantioselective organocatalysis of Strecker and Mannich reactions based on carbohydrates
-
Becker, C.; Hoben, C.; Kunz, H.; Enantioselective organocatalysis of Strecker and Mannich reactions based on carbohydrates. Adv. Synth. Catal., 2007, 349, 417-424.
-
(2007)
Adv. Synth. Catal.
, vol.349
, pp. 417-424
-
-
Becker, C.1
Hoben, C.2
Kunz, H.3
-
60
-
-
34250878930
-
Novel enantiocontrol system with aminoacyl derivatives of glucoside as enaminebased organocatalysts for aldol reaction in aqueous media
-
Tsutsui, A.; Takeda, H.; Kimura, M.; Fujimotob, T.; Machinami, T. Novel enantiocontrol system with aminoacyl derivatives of glucoside as enaminebased organocatalysts for aldol reaction in aqueous media. Tetrahedron Lett., 2007, 48, 5213-5217.
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 5213-5217
-
-
Tsutsui, A.1
Takeda, H.2
Kimura, M.3
Fujimotob, T.4
Machinami, T.5
-
61
-
-
38849111914
-
D-Glucosamine, a natural aminosugar as organocatalyst for an ecofriendly direct aldol reaction of ketones with aromatic aldehydes in water
-
Singh, N.; Pandey, J.; Tripathi, R. P. D-Glucosamine, a natural aminosugar as organocatalyst for an ecofriendly direct aldol reaction of ketones with aromatic aldehydes in water. Catal. Commun., 2008, 9, 743-746.
-
(2008)
Catal. Commun.
, vol.9
, pp. 743-746
-
-
Singh, N.1
Pandey, J.2
Tripathi, R.P.3
-
62
-
-
79956374114
-
Carbohydratederived alcohols as organocatalysts in enantioselective aldol reactions of isatins with ketones
-
Shen, C.; Shen, F.-Y.; Xia, H. J.; Zhang, P. F.; Chen, X.Z. Carbohydratederived alcohols as organocatalysts in enantioselective aldol reactions of isatins with ketones. Tetrahedron: Asymmetry 2011, 22, 708-712.
-
(2011)
Tetrahedron: Asymmetry
, vol.22
, pp. 708-712
-
-
Shen, C.1
Shen, F.-Y.2
Xia, H.J.3
Zhang, P.F.4
Chen, X.Z.5
-
63
-
-
77955797795
-
Chitosan aerogel: A recyclable, heterogeneous organocatalyst for the asymmetric direct aldol reaction in water
-
Ricci, A.; Bernardi, L.; Gioia, C.; Vierucci, S.; Robitzer, M.; Quignard, F. Chitosan aerogel: a recyclable, heterogeneous organocatalyst for the asymmetric direct aldol reaction in water. Chem. Commun., 2010, 46, 6288-6290.
-
(2010)
Chem. Commun.
, vol.46
, pp. 6288-6290
-
-
Ricci, A.1
Bernardi, L.2
Gioia, C.3
Vierucci, S.4
Robitzer, M.5
Quignard, F.6
-
64
-
-
33750796984
-
Chitosan hydrogel: A green and recyclable biopolymer catalyst for aldol and Knoevenagel reactions
-
Reddy, K. R.; Rajgopal, K.; Maheswari, C. U. Kantam, M. L. Chitosan hydrogel: A green and recyclable biopolymer catalyst for aldol and Knoevenagel reactions. New J. Chem., 2006, 30, 1549-1552.
-
(2006)
New J. Chem.
, vol.30
, pp. 1549-1552
-
-
Reddy, K.R.1
Rajgopal, K.2
Maheswari, C.U.3
Kantam, M.L.4
-
65
-
-
70349835637
-
Accessible sugars as asymmetric olefin epoxidation organocatalysts glucosaminide ketones in the synthesis of terminal epoxides
-
Boutureira, O.; McGouran, J. F.; Stafford, R. L.; Emmerson, D. P. G.; Davis, B. G. Accessible sugars as asymmetric olefin epoxidation organocatalysts glucosaminide ketones in the synthesis of terminal epoxides. Org. Biomol. Chem., 2009, 7, 4285-4288.
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 4285-4288
-
-
Boutureira, O.1
McGouran, J.F.2
Stafford, R.L.3
Emmerson, D.P.G.4
Davis, B.G.5
-
66
-
-
79955568371
-
Glucosamine-based primary amines as organocatalysts for the asymmetric Aldol reaction
-
Agarwal, J.; Peddinti, R. K. Glucosamine-based primary amines as organocatalysts for the asymmetric Aldol reaction. J. Org. Chem., 2011, 76, 3502-3505.
-
(2011)
J. Org. Chem.
, vol.76
, pp. 3502-3505
-
-
Agarwal, J.1
Peddinti, R.K.2
-
67
-
-
78649895764
-
Asymmetric Michael addition catalysed by sugarbased prolinamides in solvent-free conditions
-
Agarwal, J.; Peddinti, R K. Asymmetric Michael addition catalysed by sugarbased prolinamides in solvent-free conditions. Tetrahedron Lett., 2011, 52, 117-121.
-
(2011)
Tetrahedron Lett.
, vol.52
, pp. 117-121
-
-
Agarwal, J.1
Peddinti, R.K.2
-
68
-
-
79959588605
-
Diastereo-and enantioselective direct Aldol reactions in aqueous medium: A new highly efficient proline-sugar chimeric catalyst
-
Pedatella, S.; Nisco, M. D.; Mastroianni, D.; Naviglio, D.; Nucci, A.; Caputoa, R. Diastereo-and enantioselective direct Aldol reactions in aqueous medium: a new highly efficient proline-sugar chimeric catalyst. Adv. Synth. Catal., 2011, 353, 1443-1446
-
(2011)
Adv. Synth. Catal.
, vol.353
, pp. 1443-1446
-
-
Pedatella, S.1
Nisco, M.D.2
Mastroianni, D.3
Naviglio, D.4
Nucci, A.5
Caputoa, R.6
-
69
-
-
84862326288
-
D-Glucosamine in a chimeric prolinamide organocatalyst for direct asymmetric aldol addition
-
Nisco, M. D.; Pedatella, S.; Bektas, S.; Nucci, A.; Caputoa, R. D-Glucosamine in a chimeric prolinamide organocatalyst for direct asymmetric aldol addition. Carbohydr. Res., 2012, 356, 273-277.
-
(2012)
Carbohydr. Res.
, vol.356
, pp. 273-277
-
-
Nisco, M.D.1
Pedatella, S.2
Bektas, S.3
Nucci, A.4
Caputoa, R.5
-
70
-
-
84861427989
-
Novel carbohydrate-derived prolinamide as a highly efficient, recoverable catalyst for direct aldol reactions in water
-
Shen, C.; Shen, F. Y.; Zhou, G. B.; Xia, H. J.; Chen, X. Z.; Liu, X. G.; Zhang, P. F. Novel carbohydrate-derived prolinamide as a highly efficient, recoverable catalyst for direct aldol reactions in water. Catal. Commun., 2012, 26, 6-10.
-
(2012)
Catal. Commun.
, vol.26
, pp. 6-10
-
-
Shen, C.1
Shen, F.Y.2
Zhou, G.B.3
Xia, H.J.4
Chen, X.Z.5
Liu, X.G.6
Zhang, P.F.7
-
71
-
-
79954446272
-
Novel carbohydrate-based bifunctional organocatalysts for nucleophilic addition to nitroolefins and imines
-
Puglisi, A.; Benaglia, M.; Raimondi, L.; Lay, L.; Poletti, L. Novel carbohydrate-based bifunctional organocatalysts for nucleophilic addition to nitroolefins and imines. Org. Biomol. Chem., 2011, 9, 3295-3302.
-
(2011)
Org. Biomol. Chem.
, vol.9
, pp. 3295-3302
-
-
Puglisi, A.1
Benaglia, M.2
Raimondi, L.3
Lay, L.4
Poletti, L.5
-
72
-
-
84858771290
-
3-and 4-Uloses derived from N-acetyl-Dglucosamine: A unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes
-
Schöberl, C.; Jäger, V. 3-and 4-Uloses derived from N-acetyl-Dglucosamine: a unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes. Adv. Synth. Catal., 2012, 354, 790-796.
-
(2012)
Adv. Synth. Catal.
, vol.354
, pp. 790-796
-
-
Schöberl, C.1
Jäger, V.2
|