-
2
-
-
0001539570
-
-
Rappaport, Z, Apeloig, Y, Eds, Wiley: New York
-
(a) Ojima, I.; Li, Z.; Zhu, J. In Chemistry of Organic Silicon Compounds, Rappaport, Z., Apeloig, Y., Eds.; Wiley: New York, 1998; Vol. 2, pp 1687-1792.
-
(1998)
Chemistry of Organic Silicon Compounds
, vol.2
, pp. 1687-1792
-
-
Ojima, I.1
Li, Z.2
Zhu, J.3
-
3
-
-
0000777874
-
-
Paquette, L. A. Ed, Wiley-VCH: Weinheim, Germany
-
(b) Itsuno, S. Enantioselective Reduction of Ketones in Organic Reactions, Paquette, L. A. Ed.; Wiley-VCH: Weinheim, Germany, 1998; Vol. 52, pp 395-576.
-
(1998)
Enantioselective Reduction of Ketones in Organic Reactions
, vol.52
, pp. 395-576
-
-
Itsuno, S.1
-
4
-
-
40549145558
-
-
Jacobsen, E. N, Pfaltz, A, Yamamoto, H. Eds, Springer: Berlin, Chapter 6.3
-
(c) Nishiyama, H. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H. Eds.; Springer: Berlin, 1999. Chapter 6.3.
-
(1999)
Comprehensive Asymmetric Catalysis
-
-
Nishiyama, H.1
-
5
-
-
0036316777
-
Chemo-and Enantioselective Hydrosilylation of Carbonyl and Imino Groups. An Emphasis on Non-Traditional Catalyst Systems
-
(d) Carpentier, J. F.; Bette, V. Chemo-and Enantioselective Hydrosilylation of Carbonyl and Imino Groups. An Emphasis on Non-Traditional Catalyst Systems. Curr. Org. Chem. 2002, 6, 913-936.
-
(2002)
Curr. Org. Chem
, vol.6
, pp. 913-936
-
-
Carpentier, J.F.1
Bette, V.2
-
6
-
-
11144301117
-
Recent Advances in Asymmetric Hydrosilylation of Ketones, Imines and Electrophilic Double Bonds
-
(e) Riant, O.; Mostefaï, N.; Courmarcel, J. Recent Advances in Asymmetric Hydrosilylation of Ketones, Imines and Electrophilic Double Bonds. Synthesis 2004, 2943-2958.
-
(2004)
Synthesis
, pp. 2943-2958
-
-
Riant, O.1
Mostefaï, N.2
Courmarcel, J.3
-
8
-
-
0004246896
-
-
For complementary reviews, see: a, Krause, N, Ed, Wiley-VCH: Weinheim, Germany
-
For complementary reviews, see: (a) Lipshutz, B. H. In Modern Organocopper Chemistry, Krause, N., Ed.; Wiley-VCH: Weinheim, Germany, 2002; pp 167-187.
-
(2002)
Modern Organocopper Chemistry
, pp. 167-187
-
-
Lipshutz, B.H.1
-
9
-
-
33846485125
-
Polishing a Diamond in the Rough: "Cu-H" Catalysis with Silanes
-
(b) Rendler, S.; Oestreich, M. Polishing a Diamond in the Rough: "Cu-H" Catalysis with Silanes. Angew. Chem., Int. Ed. 2007, 46, 498-504.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 498-504
-
-
Rendler, S.1
Oestreich, M.2
-
10
-
-
36849065859
-
-
Nolan, S. P, Ed, Wiley-VCH: Weinheim, Germany
-
(a) N-Heterocyclic Carbenes in Synthesis, Nolan, S. P., Ed.; Wiley-VCH: Weinheim, Germany, 2006.
-
(2006)
N-Heterocyclic Carbenes in Synthesis
-
-
-
13
-
-
0000359191
-
Reduction of α,β-Unsaturated Carbonyl Compounds by "ate" Complexes of Copper(I) Hydride
-
For early examples, see: a
-
For early examples, see: (a) Boeckman, R. K.; Michalak, R. Reduction of α,β-Unsaturated Carbonyl Compounds by "ate" Complexes of Copper(I) Hydride. J. Am. Chem. Soc. 1974, 96, 1623-1625.
-
(1974)
J. Am. Chem. Soc
, vol.96
, pp. 1623-1625
-
-
Boeckman, R.K.1
Michalak, R.2
-
14
-
-
0000063964
-
Reductions with Copper Hydride. New Preparative and Mechanistic Aspects
-
(b) Semmelhack, M. F.; Stauffer, R. D. Reductions with Copper Hydride. New Preparative and Mechanistic Aspects. J. Org. Chem. 1975, 40, 3619-3621.
-
(1975)
J. Org. Chem
, vol.40
, pp. 3619-3621
-
-
Semmelhack, M.F.1
Stauffer, R.D.2
-
16
-
-
0000078006
-
-
Bezman, S. A.; Churchill, M. R.; Osborn, J. A.; Wormald, J. Preparation and Crystallographic Characterization of a Hexameric Triphenylphosphinecopper Hydride Cluster. J. Am. Chem. Soc. 1971, 93, 2063-2065.
-
Bezman, S. A.; Churchill, M. R.; Osborn, J. A.; Wormald, J. Preparation and Crystallographic Characterization of a Hexameric Triphenylphosphinecopper Hydride Cluster. J. Am. Chem. Soc. 1971, 93, 2063-2065.
-
-
-
-
19
-
-
0032566023
-
A Convenient, Efficient Method for Conjugate Reductions Using Catalytic Quantities of Cu(I)
-
(a) Lipshutz, B. H.; Keith, J.; Papa, P.; Vivian, R. A Convenient, Efficient Method for Conjugate Reductions Using Catalytic Quantities of Cu(I). Tetrahedron Lett. 1998, 39, 4627-4630.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4627-4630
-
-
Lipshutz, B.H.1
Keith, J.2
Papa, P.3
Vivian, R.4
-
20
-
-
0034724742
-
Copper Hydride-Catalyzed Tandem 1,4-Reduction/ Alkylation Reactions
-
(b) Lipshutz, B. H.; Chrisman, W.; Noson, K.; Papa, P.; Sclafani, J. A.; Vivian, R. W.; Keith, J. M. Copper Hydride-Catalyzed Tandem 1,4-Reduction/ Alkylation Reactions. Tetrahedron 2000, 56, 2779-2788.
-
(2000)
Tetrahedron
, vol.56
, pp. 2779-2788
-
-
Lipshutz, B.H.1
Chrisman, W.2
Noson, K.3
Papa, P.4
Sclafani, J.A.5
Vivian, R.W.6
Keith, J.M.7
-
21
-
-
2542502428
-
Asymmetric 1,4-Reductions of Hindered β-Substituted Cycloalkenones Using Catalytic SEGPHOS-Ligated CuH
-
(a) Lipshutz, B. H.; Servesko, J. M.; Petersen, T. B.; Papa, P.; Lover, A. A. Asymmetric 1,4-Reductions of Hindered β-Substituted Cycloalkenones Using Catalytic SEGPHOS-Ligated CuH. Org. Lett. 2004, 6, 1273-1275.
-
(2004)
Org. Lett
, vol.6
, pp. 1273-1275
-
-
Lipshutz, B.H.1
Servesko, J.M.2
Petersen, T.B.3
Papa, P.4
Lover, A.A.5
-
22
-
-
3142779334
-
Asymmetric 1,4-Hydrosilylations of α,β-Unsaturated Esters
-
(b) Lipshutz, B. H.; Servesko, J. M.; Taft, B. R. Asymmetric 1,4-Hydrosilylations of α,β-Unsaturated Esters. J. Am. Chem. Soc. 2004, 126, 8352-8353.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 8352-8353
-
-
Lipshutz, B.H.1
Servesko, J.M.2
Taft, B.R.3
-
23
-
-
26844454922
-
CuH in a Bottle: A Convenient Reagent for Asymmetric Hydrosilylations
-
(c) Lipshutz, B. H.; Frieman, B. A. CuH in a Bottle: A Convenient Reagent for Asymmetric Hydrosilylations. Angew. Chem., Int. Ed. 2005, 44, 6345-6348.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 6345-6348
-
-
Lipshutz, B.H.1
Frieman, B.A.2
-
24
-
-
0342316653
-
-
Achiral systems: (a) Boudjouk, P.; Kloos, S.; Rajkumar, A. B. Exclusive β-Hydrosilylation of Acrylates Catalysed by Copper- Tetramethylethylenediamine. J. Organomet. Chem. 1993, 443, C41-C43.
-
Achiral systems: (a) Boudjouk, P.; Kloos, S.; Rajkumar, A. B. Exclusive β-Hydrosilylation of Acrylates Catalysed by Copper- Tetramethylethylenediamine. J. Organomet. Chem. 1993, 443, C41-C43.
-
-
-
-
25
-
-
17144430054
-
Highly Efficient Conjugate Reduction of α,β-Unsaturated Nitrites Catalyzed by Copper/Xanthene-Type Bisphosphine Complexes
-
(b) Kim, D.; Park, B.-M.; Yun, J. Highly Efficient Conjugate Reduction of α,β-Unsaturated Nitrites Catalyzed by Copper/Xanthene-Type Bisphosphine Complexes. Chem. Commun. 2005, 1755-1757.
-
(2005)
Chem. Commun
, pp. 1755-1757
-
-
Kim, D.1
Park, B.-M.2
Yun, J.3
-
26
-
-
0033552259
-
-
Chiral systems: (c) Appella, D. H.; Moritani, Y.; Shintani, R.; Ferreira, E. M.; Buchwald, S. L. Asymmetric Conjugated Reduction of α,β- Unsaturated Esters Using a Chiral Phosphine-Copper Catalyst. J. Am. Chem. Soc. 1999, 121, 9473-9474
-
Chiral systems: (c) Appella, D. H.; Moritani, Y.; Shintani, R.; Ferreira, E. M.; Buchwald, S. L. Asymmetric Conjugated Reduction of α,β- Unsaturated Esters Using a Chiral Phosphine-Copper Catalyst. J. Am. Chem. Soc. 1999, 121, 9473-9474
-
-
-
-
27
-
-
0034686724
-
Synthesis of β-Alkyl Cyclopentanones in High Enantiomeric Excess via Copper-Catalyzed Asymmetric Conjugate Reduction
-
(d) Moritani, Y.; Apella, D. H.; Jurkauskas, V.; Buchwald, S. L. Synthesis of β-Alkyl Cyclopentanones in High Enantiomeric Excess via Copper-Catalyzed Asymmetric Conjugate Reduction. J. Am. Chem. Soc. 2000, 122, 6797-6798.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 6797-6798
-
-
Moritani, Y.1
Apella, D.H.2
Jurkauskas, V.3
Buchwald, S.L.4
-
28
-
-
25844459363
-
Dynamic Kinetic Resolution of α,β-Unsaturated Lactones Through Asymmetric Copper-Catalyzed Conjugate Reduction: Application to the Total Synthesis of Eupomatilone-3
-
(e) Rainka, M. P.; Milne, J.; Buchwald, S. L. Dynamic Kinetic Resolution of α,β-Unsaturated Lactones Through Asymmetric Copper-Catalyzed Conjugate Reduction: Application to the Total Synthesis of Eupomatilone-3. Angew. Chem., Int. Ed. 2005, 44, 6177-6180.
-
(2005)
Angew. Chem., Int. Ed
, vol.44
, pp. 6177-6180
-
-
Rainka, M.P.1
Milne, J.2
Buchwald, S.L.3
-
29
-
-
33744717835
-
Chiral Silanes via Asymmetric Hydrosilylation with Catalytic CuH
-
(f) Lipshutz, B. L.; Tanaka, N.; Taft, B. R.; Lee, C.-T. Chiral Silanes via Asymmetric Hydrosilylation with Catalytic CuH. Org. Lett. 2006, 8, 1963-1966.
-
(2006)
Org. Lett
, vol.8
, pp. 1963-1966
-
-
Lipshutz, B.L.1
Tanaka, N.2
Taft, B.R.3
Lee, C.-T.4
-
30
-
-
34547418739
-
Copper-Catalyzed Asymmetric Reduction of 3,3-Diarylacrylonitriles
-
(g) Lee, D.; Yang, Y.; Yun, J. Copper-Catalyzed Asymmetric Reduction of 3,3-Diarylacrylonitriles. Org. Lett. 2007, 9, 2749-2751.
-
(2007)
Org. Lett
, vol.9
, pp. 2749-2751
-
-
Lee, D.1
Yang, Y.2
Yun, J.3
-
31
-
-
0032506682
-
A Conjugated Reduction- Intramolecular Aldol Strategy Toward the Synthesis of Pseudolaric Acid A
-
(a) Chiu, P.; Chen, B.; Cheng, K. F. A Conjugated Reduction- Intramolecular Aldol Strategy Toward the Synthesis of Pseudolaric Acid A. Tetrahedron Lett. 1998, 39, 9229-9232.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 9229-9232
-
-
Chiu, P.1
Chen, B.2
Cheng, K.F.3
-
32
-
-
0000975755
-
Tandem Conjugate Reduction-Aldol Cyclization Using Stryker's Reagent
-
(b) Chiu, P.; Szeto, C.-P.; Geng, Z.; Cheng, K.-F. Tandem Conjugate Reduction-Aldol Cyclization Using Stryker's Reagent. Org. Lett. 2001, 3, 1901-1903.
-
(2001)
Org. Lett
, vol.3
, pp. 1901-1903
-
-
Chiu, P.1
Szeto, C.-P.2
Geng, Z.3
Cheng, K.-F.4
-
33
-
-
0035844674
-
Application of the Tandem Stryker Reduction-Aldol Cyclization Strategy to the Asymmetric Synthesis of Lucinone
-
(c) Chiu, P.; Szeto, C. P.; Geng, Z.; Cheng, K. F. Application of the Tandem Stryker Reduction-Aldol Cyclization Strategy to the Asymmetric Synthesis of Lucinone. Tetrahedron Lett. 2001, 42, 4091-4093.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 4091-4093
-
-
Chiu, P.1
Szeto, C.P.2
Geng, Z.3
Cheng, K.F.4
-
34
-
-
9144228846
-
Stoichiometric and Catalytic Reductive Aldol Cyclization of Alkynediones Induced by Stryker's Reagent
-
(a) Chiu, P.; Leung, S. K. Stoichiometric and Catalytic Reductive Aldol Cyclization of Alkynediones Induced by Stryker's Reagent. Chem. Commun. 2004, 2308-2309.
-
(2004)
Chem. Commun
, pp. 2308-2309
-
-
Chiu, P.1
Leung, S.K.2
-
35
-
-
4544221000
-
in Copper-Mediated Conjugate Reductions and Reductive Aldol Reactions
-
(b) Chiu, P. Organosilanes in Copper-Mediated Conjugate Reductions and Reductive Aldol Reactions. Synthesis 2004, 2210-2215.
-
(2004)
Synthesis
, pp. 2210-2215
-
-
Chiu1
Organosilanes, P.2
-
36
-
-
25444446131
-
Cu(I)-Catalyzed Reductive Aldol Cyclizations: Diastereo- and Enantioselective Synthesis of β- Hydroxylactones
-
(a) Lam, H. W.; Joensuu, P. M. Cu(I)-Catalyzed Reductive Aldol Cyclizations: Diastereo- and Enantioselective Synthesis of β- Hydroxylactones. Org. Lett. 2005, 7, 4225-4228.
-
(2005)
Org. Lett
, vol.7
, pp. 4225-4228
-
-
Lam, H.W.1
Joensuu, P.M.2
-
37
-
-
29444433067
-
Diastereoselective Synthesis of 4-Hydroxypiperidin-2-ones via Cu(I)-Catalyzed Reductive Aldol Cyclization
-
(b) Lam, H. W.; Murray, G. J.; Firth, J. D. Diastereoselective Synthesis of 4-Hydroxypiperidin-2-ones via Cu(I)-Catalyzed Reductive Aldol Cyclization. Org. Lett. 2005, 7, 5743-5746.
-
(2005)
Org. Lett
, vol.7
, pp. 5743-5746
-
-
Lam, H.W.1
Murray, G.J.2
Firth, J.D.3
-
38
-
-
33744913650
-
Highly Diastereo- and Enantioselective Copper-Catalyzed Domino Reduction/Aldol Reaction of Ketones with Methyl Acrylate
-
(c) Deschamp, J.; Chuzel, O.; Hannedouche, J.; Riant, O. Highly Diastereo- and Enantioselective Copper-Catalyzed Domino Reduction/Aldol Reaction of Ketones with Methyl Acrylate. Angew. Chem., Int. Ed. 2006, 45, 1292-1297.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 1292-1297
-
-
Deschamp, J.1
Chuzel, O.2
Hannedouche, J.3
Riant, O.4
-
39
-
-
33744923178
-
Catalytic Enantioselective Aldol Reaction to Ketones
-
(d) Oisaki, K.; Zhao, D. B.; Kanai, M.; Shibasaki, M. Catalytic Enantioselective Aldol Reaction to Ketones. J. Am. Chem. Soc. 2006, 128, 7164-7165.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 7164-7165
-
-
Oisaki, K.1
Zhao, D.B.2
Kanai, M.3
Shibasaki, M.4
-
40
-
-
33750969372
-
Dramatic Ligand Effect in Catalytic Asymmetric Reductive Aldol Reaction of Allenic Esters to Ketones
-
(e) Zhao, D. B.; Oisaki, K.; Kanai, M.; Shibasaki, M. Dramatic Ligand Effect in Catalytic Asymmetric Reductive Aldol Reaction of Allenic Esters to Ketones. J. Am. Chem. Soc. 2006, 128, 14440-14441.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 14440-14441
-
-
Zhao, D.B.1
Oisaki, K.2
Kanai, M.3
Shibasaki, M.4
-
41
-
-
33846137282
-
Copper(I)-Catalyzed Enantio- and Diastereoselective Tandem Reductive Aldol Reaction
-
(f) Chuzel, O.; Deschamp, J.; Chausteur, C.; Riant, O. Copper(I)-Catalyzed Enantio- and Diastereoselective Tandem Reductive Aldol Reaction. Org Lett. 2006, 8, 5943-5946.
-
(2006)
Org Lett
, vol.8
, pp. 5943-5946
-
-
Chuzel, O.1
Deschamp, J.2
Chausteur, C.3
Riant, O.4
-
42
-
-
33846176873
-
A Three-Component Tandem Reductive Aldol Reaction Catalyzed by N-Heterocyclic Carbene-Copper Complexes
-
Welle, A.; Díez-González, S.; Tinant, B.; Nolan, S. P.; Riant, O. A Three-Component Tandem Reductive Aldol Reaction Catalyzed by N-Heterocyclic Carbene-Copper Complexes. Org. Lett. 2006, 8, 6059-6062.
-
(2006)
Org. Lett
, vol.8
, pp. 6059-6062
-
-
Welle, A.1
Díez-González, S.2
Tinant, B.3
Nolan, S.P.4
Riant, O.5
-
43
-
-
0030733481
-
Generation of a Reducing Reagent from Copper(I) Salt and Hydrosilane. New Practical Method for Conjugate Reduction
-
Ito, H.; Ishizuka, T.; Arimoto, K.; Miura, K.; Hosomi, A. Generation of a Reducing Reagent from Copper(I) Salt and Hydrosilane. New Practical Method for Conjugate Reduction. Tetrahedron Lett. 1997, 38, 8887-8890.
-
(1997)
Tetrahedron Lett
, vol.38
, pp. 8887-8890
-
-
Ito, H.1
Ishizuka, T.2
Arimoto, K.3
Miura, K.4
Hosomi, A.5
-
44
-
-
0034087505
-
New Reactivity of a Reducing Agent Generated from a Copper(I) Salt and a Hydrosilane: Selective Reduction of Ketones and Olefins Conjugated with an Aromatic Group
-
Ito, H.; Yamanaka, H.; Ishizuka, T.; Takeiwa, J.-i.; Hosomi, A. New Reactivity of a Reducing Agent Generated from a Copper(I) Salt and a Hydrosilane: Selective Reduction of Ketones and Olefins Conjugated with an Aromatic Group. Synlett 2000, 479-482.
-
(2000)
Synlett
, pp. 479-482
-
-
Ito, H.1
Yamanaka, H.2
Ishizuka, T.3
Takeiwa, J.-I.4
Hosomi, A.5
-
46
-
-
0141520660
-
Tweaking Copper Hydride (CuH) for Synthetic Gain. A Practical, One-Pot Conversion of Dialkyl Ketones to Reduced Trialkylsilyl Ether Derivatives
-
Lipshutz, B. H.; Caires, C. C.; Kuipers, P.; Chrisman, W. Tweaking Copper Hydride (CuH) for Synthetic Gain. A Practical, One-Pot Conversion of Dialkyl Ketones to Reduced Trialkylsilyl Ether Derivatives. Org. Lett. 2003, 5, 3085-3088.
-
(2003)
Org. Lett
, vol.5
, pp. 3085-3088
-
-
Lipshutz, B.H.1
Caires, C.C.2
Kuipers, P.3
Chrisman, W.4
-
47
-
-
0035956540
-
Ligand-Accelerated, Copper-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones
-
(a) Lipshutz, B. H.; Noson, K.; Chrisman, W. Ligand-Accelerated, Copper-Catalyzed Asymmetric Hydrosilylation of Aryl Ketones. J. Am. Chem. Soc. 2001, 123, 12917-12918.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 12917-12918
-
-
Lipshutz, B.H.1
Noson, K.2
Chrisman, W.3
-
48
-
-
0037960828
-
Asymmetric Hydrosilylation of Aryl Ketones Catalyzed by Copper Hydride Complexed by Nonracemic Biphenyl Bis-phosphine Ligands
-
(b) Lipshutz, B. H.; Noson, K.; Chrisman, W.; Lower, A. Asymmetric Hydrosilylation of Aryl Ketones Catalyzed by Copper Hydride Complexed by Nonracemic Biphenyl Bis-phosphine Ligands. J. Am. Chem. Soc. 2003, 125, 8779-8789.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 8779-8789
-
-
Lipshutz, B.H.1
Noson, K.2
Chrisman, W.3
Lower, A.4
-
49
-
-
0038581793
-
Copper(I) Hydride-Catalyzed Asymmetric Hydrosilylation of Heteroaromatic Ketones
-
Lipshutz, B. H.; Lower, A.; Noson, K. Copper(I) Hydride-Catalyzed Asymmetric Hydrosilylation of Heteroaromatic Ketones. Org. Lett. 2002, 4, 4045-4048.
-
(2002)
Org. Lett
, vol.4
, pp. 4045-4048
-
-
Lipshutz, B.H.1
Lower, A.2
Noson, K.3
-
50
-
-
0001865938
-
Copper(I) Salt Mediated 1,4-Reduction of α,β-Unsaturated Ketones Using Hydrosilanes
-
(a) Mori, A.; Fujita, A.; Nishihara, Y.; Hiyama, T. Copper(I) Salt Mediated 1,4-Reduction of α,β-Unsaturated Ketones Using Hydrosilanes. Chem. Commun. 1997, 2159-2160.
-
(1997)
Chem. Commun
, pp. 2159-2160
-
-
Mori, A.1
Fujita, A.2
Nishihara, Y.3
Hiyama, T.4
-
51
-
-
0033537956
-
Conjugate Reduction of α,β-Unsaturated Ketones with Hydrosilane Mediated by Copper(I) Salt
-
(b) Mori, A.; Fujita, A.; Kajiro, H.; Nishihara, Y.; Hiyama, T. Conjugate Reduction of α,β-Unsaturated Ketones with Hydrosilane Mediated by Copper(I) Salt. Tetrahedron 1999, 55, 4573-4582.
-
(1999)
Tetrahedron
, vol.55
, pp. 4573-4582
-
-
Mori, A.1
Fujita, A.2
Kajiro, H.3
Nishihara, Y.4
Hiyama, T.5
-
52
-
-
0000187570
-
Efficient Enantioselective Hydrosilylation of Ketones Catalyzed by Air Stable Copper Fluoride-Phosphine Complexes
-
Sirol, S.; Courmarcel, J.; Mostefai, N.; Riant, O. Efficient Enantioselective Hydrosilylation of Ketones Catalyzed by Air Stable Copper Fluoride-Phosphine Complexes. Org. Lett. 2001, 3, 4111-4113.
-
(2001)
Org. Lett
, vol.3
, pp. 4111-4113
-
-
Sirol, S.1
Courmarcel, J.2
Mostefai, N.3
Riant, O.4
-
53
-
-
34247576904
-
Air-Accelerated Enantioselective Hidrosilylation of Ketones Catalyzed by Copper(I) Fluoride-Diphosphine Complexes: Investigations of the Effects of Temperature and Ligand Structure
-
See also
-
See also: Mostefaï, N.; Sirol, S.; Courmarcel, J.; Riant, O. Air-Accelerated Enantioselective Hidrosilylation of Ketones Catalyzed by Copper(I) Fluoride-Diphosphine Complexes: Investigations of the Effects of Temperature and Ligand Structure. Synthesis 2007, 1265-1271.
-
(2007)
Synthesis
, pp. 1265-1271
-
-
Mostefaï, N.1
Sirol, S.2
Courmarcel, J.3
Riant, O.4
-
54
-
-
14844346911
-
A Remarkably Effective Copper(II)-Dipyridylphosphine Catalyst System for the Asymmetric Hydrosilylation of Ketones in Air
-
Wu, J.; Ji, J.-X.; Chan, A. S. C. A Remarkably Effective Copper(II)-Dipyridylphosphine Catalyst System for the Asymmetric Hydrosilylation of Ketones in Air. Proc. Natl. Acad. Sci. U.S.A. 2005, 102, 3570-3575.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A
, vol.102
, pp. 3570-3575
-
-
Wu, J.1
Ji, J.-X.2
Chan, A.S.C.3
-
56
-
-
28844444555
-
A New and Effective Method for Providing Optically Active Monosubstituted Malononitriles: Selective Reduction of α,β-Unsaturated Dinitriles Catalyzed by Copper Hydride Complexes
-
Ren, Y.; Xu, X.; Sun, K.; Xu, J. A New and Effective Method for Providing Optically Active Monosubstituted Malononitriles: Selective Reduction of α,β-Unsaturated Dinitriles Catalyzed by Copper Hydride Complexes. Tetrahedron: Asymmetry 2005, 16, 4010-4014.
-
(2005)
Tetrahedron: Asymmetry
, vol.16
, pp. 4010-4014
-
-
Ren, Y.1
Xu, X.2
Sun, K.3
Xu, J.4
-
57
-
-
33749327878
-
Efficient Enantioselective Hydrosilylation of Aryl Ketones Catalyzed by a Chiral BINAP-Copper(I) Catalyst-Phenyl-(methyl)silane System
-
Issenhuth, J. T.; Dagorne, S.; Bellemin-Laponnaz, S. Efficient Enantioselective Hydrosilylation of Aryl Ketones Catalyzed by a Chiral BINAP-Copper(I) Catalyst-Phenyl-(methyl)silane System. Adv. Synth. Catal. 2006, 348, 1991-1994.
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 1991-1994
-
-
Issenhuth, J.T.1
Dagorne, S.2
Bellemin-Laponnaz, S.3
-
59
-
-
0141631426
-
Conjugated Reduction of α,β-Unsaturated Carbonyl Compounds Catalyzed by a Copper Carbene Complex
-
Jurkauskas, V.; Sadighi, J. P.; Buchwald, S. L. Conjugated Reduction of α,β-Unsaturated Carbonyl Compounds Catalyzed by a Copper Carbene Complex. Org. Lett. 2003, 5, 2417-2420.
-
(2003)
Org. Lett
, vol.5
, pp. 2417-2420
-
-
Jurkauskas, V.1
Sadighi, J.P.2
Buchwald, S.L.3
-
60
-
-
1542647135
-
I (NHC = N-Heterocyclic Carbene) Complexes as Efficient Catalysts for the Reduction of Carbonyl Compounds
-
I (NHC = N-Heterocyclic Carbene) Complexes as Efficient Catalysts for the Reduction of Carbonyl Compounds. Organometallics 2004, 23, 1157-1160.
-
(2004)
Organometallics
, vol.23
, pp. 1157-1160
-
-
Kaur, H.1
Zinn, F.K.2
Stevens, E.D.3
Nolan, S.P.4
-
61
-
-
27944464064
-
-
2-3,4,5,6-tetrahydropyrimidin-2-ylidenes (R = Mesityl, 2-Propyl): Synthesis, X-Ray Structures, Inmobilization and Catalytic Activity. Tetrahedron 2005, 61, 12145-12152.
-
2-3,4,5,6-tetrahydropyrimidin-2-ylidenes (R = Mesityl, 2-Propyl): Synthesis, X-Ray Structures, Inmobilization and Catalytic Activity. Tetrahedron 2005, 61, 12145-12152.
-
-
-
-
62
-
-
20344396372
-
A Simple and Efficient Copper-Catalyzed Procedure for the Hydrosilylation of Hindered and Functionalized Ketones
-
Díez-González, S.; Kaur, H.; Zinn, F. K.; Stevens, E. D.; Nolan, S. P. A Simple and Efficient Copper-Catalyzed Procedure for the Hydrosilylation of Hindered and Functionalized Ketones. J. Org. Chem. 2005, 70, 4784-4796.
-
(2005)
J. Org. Chem
, vol.70
, pp. 4784-4796
-
-
Díez-González, S.1
Kaur, H.2
Zinn, F.K.3
Stevens, E.D.4
Nolan, S.P.5
-
63
-
-
33846797894
-
Stereoelectronic Parameters Associated with N-Heterocyclic Carbenes (NHC) Ligands: A Quest for Understanding
-
For a comprehensive discussion on the stereoelectronic nature of NHC ligands, see
-
For a comprehensive discussion on the stereoelectronic nature of NHC ligands, see: Díez-González, S.; Nolan, S. P. Stereoelectronic Parameters Associated with N-Heterocyclic Carbenes (NHC) Ligands: A Quest for Understanding. Coord. Chem. Rev. 2007, 251, 874-883.
-
(2007)
Coord. Chem. Rev
, vol.251
, pp. 874-883
-
-
Díez-González, S.1
Nolan, S.P.2
-
64
-
-
27744571142
-
A New Alternative to Stryker's Reagent in Hydrosilylation: Synthesis, Structure, and Reactivity of a Well-Defined Carbene-Copper(II) Acetate Complex
-
Yun, J.; Kim, D.; Yun, H. A New Alternative to Stryker's Reagent in Hydrosilylation: Synthesis, Structure, and Reactivity of a Well-Defined Carbene-Copper(II) Acetate Complex. Chem. Commun. 2005, 5181-5183.
-
(2005)
Chem. Commun
, pp. 5181-5183
-
-
Yun, J.1
Kim, D.2
Yun, H.3
-
65
-
-
33646413657
-
Cationic Copper(I) Complexes as Efficient Precatalysts for the Hydrosilylation of Carbonyl Compounds
-
(a) Díez-González, S.; Scott, N. M.; Nolan, S. P. Cationic Copper(I) Complexes as Efficient Precatalysts for the Hydrosilylation of Carbonyl Compounds. Organometallics 2006, 25, 2355-2358.
-
(2006)
Organometallics
, vol.25
, pp. 2355-2358
-
-
Díez-González, S.1
Scott, N.M.2
Nolan, S.P.3
-
67
-
-
3142668405
-
Synthesis, Structure, and Alkyne Reactivity of a Dimeric (Carbene)copper(I) Hydride
-
Mankad, N. P.; Laitar, D. S.; Sadighi, J. P. Synthesis, Structure, and Alkyne Reactivity of a Dimeric (Carbene)copper(I) Hydride. Organometallics 2004, 23, 3369-3371.
-
(2004)
Organometallics
, vol.23
, pp. 3369-3371
-
-
Mankad, N.P.1
Laitar, D.S.2
Sadighi, J.P.3
-
68
-
-
0000816349
-
An Efficient Catalyst for the Conversion of Hydrosilanes to Alkoxysilanes
-
Lorenz, C.; Schubert, U. An Efficient Catalyst for the Conversion of Hydrosilanes to Alkoxysilanes. Chem. Ber. 1995, 128, 1267-1269.
-
(1995)
Chem. Ber
, vol.128
, pp. 1267-1269
-
-
Lorenz, C.1
Schubert, U.2
-
69
-
-
0000320402
-
-
Ito, H. Ishizuka, T. Okumura, T. Yamanaka, H. Tateiwa, J.-i. Sonoda, M. Hosomi, A. Highly Stereoselective Metathesis Reaction Between Optically Active Hydrosilane and Copper(I) Salt in 1,3-Dimethyl-2-imidazolidione. J. Organomet. Chem. 1999, 574, 102-106. See also refs 19 and 20.
-
Ito, H. Ishizuka, T. Okumura, T. Yamanaka, H. Tateiwa, J.-i. Sonoda, M. Hosomi, A. Highly Stereoselective Metathesis Reaction Between Optically Active Hydrosilane and Copper(I) Salt in 1,3-Dimethyl-2-imidazolidione. J. Organomet. Chem. 1999, 574, 102-106. See also refs 19 and 20.
-
-
-
-
70
-
-
34250870731
-
N-Heterocyclic Carbenes as Organocatalysts
-
For a review, see
-
For a review, see: Marion, M.; Díez-González, S.; Nolan, S. P. N-Heterocyclic Carbenes as Organocatalysts. Angew. Chem., Int. Ed. 2007, 46, 2988-3000.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 2988-3000
-
-
Marion, M.1
Díez-González, S.2
Nolan, S.P.3
-
71
-
-
36549000812
-
Encapsulated N-Heterocyclic Carbenes in Silicones without Reactivity Modification
-
See also reference 11b and
-
See also reference 11b and: Bonnette, F.; Kato, T.; Destarac, M.; Mignani, G.; Cossío, F. P. M.; Baceiredo, A. Encapsulated N-Heterocyclic Carbenes in Silicones without Reactivity Modification. Angew. Chem., Int. Ed. 2007, 46, 8632-8635.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 8632-8635
-
-
Bonnette, F.1
Kato, T.2
Destarac, M.3
Mignani, G.4
Cossío, F.P.M.5
Baceiredo, A.6
-
72
-
-
0343480998
-
-
Saegusa, T.; Ito, Y.; Kobayashi, S.; Hirota, K. Synthetic Reactions by a Complex Catalyst. VI. A Novel Hydrosilylation of Isocyanide by Copper Catalyst. J. Am. Chem. Soc. 1967, 89, 2240-2241.
-
Saegusa, T.; Ito, Y.; Kobayashi, S.; Hirota, K. Synthetic Reactions by a Complex Catalyst. VI. A Novel Hydrosilylation of Isocyanide by Copper Catalyst. J. Am. Chem. Soc. 1967, 89, 2240-2241.
-
-
-
-
73
-
-
3142710052
-
Copper(I)-Catalyzed Asymmetric Hydrosilylations of Imines at Ambient Temperatures
-
Lipshutz, B. H.; Shimizu, H. Copper(I)-Catalyzed Asymmetric Hydrosilylations of Imines at Ambient Temperatures. Angew. Chem., Int. Ed. 2004, 43, 2228-2230.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 2228-2230
-
-
Lipshutz, B.H.1
Shimizu, H.2
-
74
-
-
33746198775
-
Copper-in-Charcoal (Cu/C): Heterogeneous, Copper-Catalyzed Asymmetric Hydrosilylation
-
Lipshutz, B. H.; Frieman, B. A.; Tomaso, A. E. Copper-in-Charcoal (Cu/C): Heterogeneous, Copper-Catalyzed Asymmetric Hydrosilylation. Angew. Chem., Int. Ed. 2006, 45, 1259-1264.
-
(2006)
Angew. Chem., Int. Ed
, vol.45
, pp. 1259-1264
-
-
Lipshutz, B.H.1
Frieman, B.A.2
Tomaso, A.E.3
-
76
-
-
0000789894
-
Copper(II)-Mediated Stereoselective Reduction of Acetylenic Sulfones by Hydrosilanes
-
Ryu, I.; Kusumoto, N.; Ogawa, A.; Kambe, N.; Sonoda, N. Copper(II)-Mediated Stereoselective Reduction of Acetylenic Sulfones by Hydrosilanes. Organometallics 1989, 8, 2279-2281.
-
(1989)
Organometallics
, vol.8
, pp. 2279-2281
-
-
Ryu, I.1
Kusumoto, N.2
Ogawa, A.3
Kambe, N.4
Sonoda, N.5
-
77
-
-
34248146411
-
Small but Effective: Copper Hydride Catalyzed Synthesis of α-Hydroxyallenes
-
Deutsch, C.; Lipshutz, B. H.; Krause, N. Small but Effective: Copper Hydride Catalyzed Synthesis of α-Hydroxyallenes. Angew. Chem., Int. Ed. 2007, 46, 1650-1653.
-
(2007)
Angew. Chem., Int. Ed
, vol.46
, pp. 1650-1653
-
-
Deutsch, C.1
Lipshutz, B.H.2
Krause, N.3
-
79
-
-
33749519443
-
Silver-Catalyzed Hydrosilylation of Aldehydes
-
Wile, B. M.; Stradiotto, M. Silver-Catalyzed Hydrosilylation of Aldehydes. Chem. Commun. 2006, 4104-4106.
-
(2006)
Chem. Commun
, pp. 4104-4106
-
-
Wile, B.M.1
Stradiotto, M.2
-
80
-
-
0034616830
-
First Gold Complex-Catalyzed Selective Hydrosilylation of Organic Compounds
-
(a) Ito, H.; Yajima, T.; Tateiwa, J.-i.; Hosomi, A. First Gold Complex-Catalyzed Selective Hydrosilylation of Organic Compounds. Chem. Commun. 2000, 981-982.
-
(2000)
Chem. Commun
, pp. 981-982
-
-
Ito, H.1
Yajima, T.2
Tateiwa, J.-I.3
Hosomi, A.4
-
81
-
-
13444273196
-
Hydrosilylation of 1-Hexyne Promoted by Acetone Solvated Gold Atoms Derived Catalysts
-
(b) Caporusso, A. M.; Aronica, L. A.; Schiavi, E.; Martra, G.; Vitulli, G.; Salvadori, P. Hydrosilylation of 1-Hexyne Promoted by Acetone Solvated Gold Atoms Derived Catalysts. J. Organomet. Chem. 2005, 690, 1063-1066.
-
(2005)
J. Organomet. Chem
, vol.690
, pp. 1063-1066
-
-
Caporusso, A.M.1
Aronica, L.A.2
Schiavi, E.3
Martra, G.4
Vitulli, G.5
Salvadori, P.6
-
82
-
-
0000286698
-
Hydrosilylation Reactions Catalyzed by Supported Bimetallic Colloids
-
(c) Schmid, G.; West, H.; Mehles, H.; Lehnert, A. Hydrosilylation Reactions Catalyzed by Supported Bimetallic Colloids. Inorg. Chem. 1997, 36, 891-895.
-
(1997)
Inorg. Chem
, vol.36
, pp. 891-895
-
-
Schmid, G.1
West, H.2
Mehles, H.3
Lehnert, A.4
-
83
-
-
33749020799
-
Fluourous Phosphine-Assisted Recycling of Gold Catalysts for Hydrosilylation of Aldehydes
-
Lantos, D.; Contel, M.; Larrea, A.; Szabó, D.; Horváth, I. T. Fluourous Phosphine-Assisted Recycling of Gold Catalysts for Hydrosilylation of Aldehydes. QSAR Comb. Sci. 2006, 25, 719-722.
-
(2006)
QSAR Comb. Sci
, vol.25
, pp. 719-722
-
-
Lantos, D.1
Contel, M.2
Larrea, A.3
Szabó, D.4
Horváth, I.T.5
-
84
-
-
33847268226
-
Au(I) Complexes Supported by Donor-Functionalized lndene Ligands: Synthesis, Characterization, and Catalytic Behavior in Aldehyde Hydrosilylation
-
Wile, B. M.; McDonald, R.; Ferguson, M. J.; Stradiotto, M. Au(I) Complexes Supported by Donor-Functionalized lndene Ligands: Synthesis, Characterization, and Catalytic Behavior in Aldehyde Hydrosilylation. Organometallics 2007, 26, 1069-1076.
-
(2007)
Organometallics
, vol.26
, pp. 1069-1076
-
-
Wile, B.M.1
McDonald, R.2
Ferguson, M.J.3
Stradiotto, M.4
-
85
-
-
0000888678
-
Homo- and Heteronuclear Cluster Compounds of Gold
-
(a) Hall, K. P.; Mingos, M. P. Homo- and Heteronuclear Cluster Compounds of Gold. Prog. Inorg. Chem. 1984, 32, 237-325.
-
(1984)
Prog. Inorg. Chem
, vol.32
, pp. 237-325
-
-
Hall, K.P.1
Mingos, M.P.2
-
86
-
-
84982504641
-
-
6-ein Goldcluster Ungewöhnlicher Grösse. Chem. Ber. 1981, 114, 3634-3642.
-
6-ein Goldcluster Ungewöhnlicher Grösse. Chem. Ber. 1981, 114, 3634-3642.
-
-
-
-
87
-
-
33947221435
-
Homogeneous Gold-Catalyzed Hydrosilylation of Aldehydes
-
Lantos, D.; Contel, M.; Sanz, S.; Bodor, A.; Horváth, I. T. Homogeneous Gold-Catalyzed Hydrosilylation of Aldehydes. J. Organomet. Chem. 2007, 692, 1799-1805.
-
(2007)
J. Organomet. Chem
, vol.692
, pp. 1799-1805
-
-
Lantos, D.1
Contel, M.2
Sanz, S.3
Bodor, A.4
Horváth, I.T.5
-
88
-
-
0033617302
-
Methylene-Bridged P-Chiral Diphosphines in Highly Enantioselective Reactions
-
Yamanoi, Y.; Imamoto, T. Methylene-Bridged P-Chiral Diphosphines in Highly Enantioselective Reactions. J. Org. Chem. 1999, 64, 2988-2989.
-
(1999)
J. Org. Chem
, vol.64
, pp. 2988-2989
-
-
Yamanoi, Y.1
Imamoto, T.2
-
89
-
-
0037131584
-
Application of a New Family of P,N Ligands to the High Enantioselective Hydrosilylation of Aryl Alkyl and Dialkyl Ketones
-
Tao, B.; Fu, G. C. Application of a New Family of P,N Ligands to the High Enantioselective Hydrosilylation of Aryl Alkyl and Dialkyl Ketones. Angew. Chem., Int. Ed. 2002, 41, 3892-3894.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 3892-3894
-
-
Tao, B.1
Fu, G.C.2
|