-
1
-
-
0034249671
-
The Heck reaction as a sharpening stone of palladium catalysis
-
Beletskaya I.P., Cheprakov A.V. The Heck reaction as a sharpening stone of palladium catalysis. Chem. Rev. 2000, 100:3009-3066.
-
(2000)
Chem. Rev.
, vol.100
, pp. 3009-3066
-
-
Beletskaya, I.P.1
Cheprakov, A.V.2
-
2
-
-
0001551026
-
Arylation of olefin with aryl iodide catalyzed by palladium
-
Mazoroki T., Mori K., Ozaki A. Arylation of olefin with aryl iodide catalyzed by palladium. Bull. Chem. Soc. Jpn. 1971, 44:581.
-
(1971)
Bull. Chem. Soc. Jpn.
, vol.44
, pp. 581
-
-
Mazoroki, T.1
Mori, K.2
Ozaki, A.3
-
3
-
-
33645896595
-
Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides
-
Heck R.F., Nolley J.J.P. Palladium-catalyzed vinylic hydrogen substitution reactions with aryl, benzyl, and styryl halides. J. Org. Chem. 1972, 37:2320-2322.
-
(1972)
J. Org. Chem.
, vol.37
, pp. 2320-2322
-
-
Heck, R.F.1
Nolley, J.J.P.2
-
4
-
-
0034838172
-
A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions
-
Littke A.F., Fu G.C. A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions. J. Am. Chem. Soc. 2001, 123:6989-7000.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 6989-7000
-
-
Littke, A.F.1
Fu, G.C.2
-
5
-
-
33745521123
-
N,N-dimethyl-beta-alanine as an inexpensive and efficient ligand for palladium-catalyzed Heck reaction
-
Cui X., Li Z., Tao C.Z., Xu Y., Li J., Liu L., Guo Q.X. N,N-dimethyl-beta-alanine as an inexpensive and efficient ligand for palladium-catalyzed Heck reaction. Org. Lett. 2006, 8:2467-2470.
-
(2006)
Org. Lett.
, vol.8
, pp. 2467-2470
-
-
Cui, X.1
Li, Z.2
Tao, C.Z.3
Xu, Y.4
Li, J.5
Liu, L.6
Guo, Q.X.7
-
6
-
-
81855172001
-
Nickel-catalyzed Heck-type reactions of benzyl chlorides and simple olefins
-
Matsubara R., Gutierrez A.C., Jamison T.F. Nickel-catalyzed Heck-type reactions of benzyl chlorides and simple olefins. J. Am. Chem. Soc. 2011, 133:19020-19023.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 19020-19023
-
-
Matsubara, R.1
Gutierrez, A.C.2
Jamison, T.F.3
-
7
-
-
0037012743
-
Concise total synthesis of (-)-frondosin B using a novel palladium-catalyzed cyclization
-
Hughes C.C., Trauner D. Concise total synthesis of (-)-frondosin B using a novel palladium-catalyzed cyclization. Angew. Chem. Int. Ed. 2002, 41:1569-1572.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 1569-1572
-
-
Hughes, C.C.1
Trauner, D.2
-
8
-
-
0038584673
-
Recent developments and new perspectives in the Heck reaction
-
Cabri W., Candiani I. Recent developments and new perspectives in the Heck reaction. Acc. Chem. Res. 1995, 28:2-7.
-
(1995)
Acc. Chem. Res.
, vol.28
, pp. 2-7
-
-
Cabri, W.1
Candiani, I.2
-
9
-
-
84861536355
-
Mechanistic studies on the Pd-catalyzed direct C&H arylation of 2-substituted thiophene derivatives with arylpalladium bipyridyl complexes
-
Steinmetz M., Ueda K., Grimme S., Yamaguchi J., Kirchberg S., Itami K., Studer A. Mechanistic studies on the Pd-catalyzed direct C&H arylation of 2-substituted thiophene derivatives with arylpalladium bipyridyl complexes. Chem. Asian J. 2012, 7:1256-1260.
-
(2012)
Chem. Asian J.
, vol.7
, pp. 1256-1260
-
-
Steinmetz, M.1
Ueda, K.2
Grimme, S.3
Yamaguchi, J.4
Kirchberg, S.5
Itami, K.6
Studer, A.7
-
10
-
-
82455205837
-
Mechanistic origin of ligand-controlled regioselectivity in Pd-Catalyzed C-H activation/arylation of thiophenes
-
Tang S.Y., Guo Q.X., Fu Y. Mechanistic origin of ligand-controlled regioselectivity in Pd-Catalyzed C-H activation/arylation of thiophenes. Chem. Eur. J. 2011, 17:13866-13876.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 13866-13876
-
-
Tang, S.Y.1
Guo, Q.X.2
Fu, Y.3
-
11
-
-
79952050537
-
Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: otherwise difficult C4-selective C-H arylation enabled by boronic acids
-
Kirchberg S., Tani S., Ueda K., Yamaguchi J., Studer A., Itami K. Oxidative biaryl coupling of thiophenes and thiazoles with arylboronic acids through palladium catalysis: otherwise difficult C4-selective C-H arylation enabled by boronic acids. Angew. Chem. Int. Ed. 2011, 50:2387-2391.
-
(2011)
Angew. Chem. Int. Ed.
, vol.50
, pp. 2387-2391
-
-
Kirchberg, S.1
Tani, S.2
Ueda, K.3
Yamaguchi, J.4
Studer, A.5
Itami, K.6
-
12
-
-
78449231481
-
A general catalyst for the beta-selective C-H bond arylation of thiophenes with iodoarenes
-
Ueda K., Yanagisawa S., Yamaguchi J., Itami K. A general catalyst for the beta-selective C-H bond arylation of thiophenes with iodoarenes. Angew. Chem. Int. Ed. 2010, 49:8946-8949.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, pp. 8946-8949
-
-
Ueda, K.1
Yanagisawa, S.2
Yamaguchi, J.3
Itami, K.4
-
13
-
-
70350054836
-
Programmed synthesis of tetraarylthiophenes through sequential C-H arylation
-
Yanagisawa S., Ueda K., Sekizawa H., Itami K. Programmed synthesis of tetraarylthiophenes through sequential C-H arylation. J. Am. Chem. Soc. 2009, 131:14622-14623.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 14622-14623
-
-
Yanagisawa, S.1
Ueda, K.2
Sekizawa, H.3
Itami, K.4
-
14
-
-
0037562071
-
Regioselective palladium-catalyzed arylation of 3-carboalkoxy furan and thiophene
-
Glover B., Harvey K.A., Liu B., Sharp M.J., Tymoschenko M.F. Regioselective palladium-catalyzed arylation of 3-carboalkoxy furan and thiophene. Org. Lett. 2003, 5:301-304.
-
(2003)
Org. Lett.
, vol.5
, pp. 301-304
-
-
Glover, B.1
Harvey, K.A.2
Liu, B.3
Sharp, M.J.4
Tymoschenko, M.F.5
-
15
-
-
0037771626
-
Simple construction of bicyclo[4.3.0]nonane, bicyclo[3.3-0]octane, and related benzo derivatives by palladium-catalyzed cycloalkenylation
-
Toyota M., Ilangovan A., Okamoto R., Masaki T., Arakawa M., Ihara M. Simple construction of bicyclo[4.3.0]nonane, bicyclo[3.3-0]octane, and related benzo derivatives by palladium-catalyzed cycloalkenylation. Org. Lett. 2002, 4:4293-4296.
-
(2002)
Org. Lett.
, vol.4
, pp. 4293-4296
-
-
Toyota, M.1
Ilangovan, A.2
Okamoto, R.3
Masaki, T.4
Arakawa, M.5
Ihara, M.6
-
16
-
-
1342327964
-
Heck-type arylation of 2-cycloalken-1-ones with arylpalladium intermediates formed by decarboxylative palladation and by aryl iodide insertion
-
Tanaka D., Myers A.G. Heck-type arylation of 2-cycloalken-1-ones with arylpalladium intermediates formed by decarboxylative palladation and by aryl iodide insertion. Org. Lett. 2004, 6:433-436.
-
(2004)
Org. Lett.
, vol.6
, pp. 433-436
-
-
Tanaka, D.1
Myers, A.G.2
-
17
-
-
72449170089
-
Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage
-
Ackermann L., Vicente R., Kapdi A.R. Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage. Angew. Chem. Int. Ed. 2009, 48:9792-9826.
-
(2009)
Angew. Chem. Int. Ed.
, vol.48
, pp. 9792-9826
-
-
Ackermann, L.1
Vicente, R.2
Kapdi, A.R.3
-
18
-
-
33846918696
-
Aryl-aryl bond formation by transition-metal-catalyzed direct arylation
-
Alberico D., Scott M.E., Lautens M. Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. Chem. Rev. 2007, 107:174-238.
-
(2007)
Chem. Rev.
, vol.107
, pp. 174-238
-
-
Alberico, D.1
Scott, M.E.2
Lautens, M.3
-
19
-
-
0142042916
-
Synthesis of novel tetracycles via an intramolecular Heck reaction with anti-hydride elimination
-
Lautens M., Fang Y.Q. Synthesis of novel tetracycles via an intramolecular Heck reaction with anti-hydride elimination. Org. Lett. 2003, 5:3679-3682.
-
(2003)
Org. Lett.
, vol.5
, pp. 3679-3682
-
-
Lautens, M.1
Fang, Y.Q.2
-
21
-
-
34250655628
-
Direct transition metal-catalyzed functionalization of heteroaromatic compounds
-
Seregin I.V., Gevorgyan V. Direct transition metal-catalyzed functionalization of heteroaromatic compounds. Chem. Soc. Rev. 2007, 36:1173-1193.
-
(2007)
Chem. Soc. Rev.
, vol.36
, pp. 1173-1193
-
-
Seregin, I.V.1
Gevorgyan, V.2
-
22
-
-
0042728760
-
Mechanisms of intramolecular activation of C-H bonds in transition-metal complexes
-
Ryabov A.D. Mechanisms of intramolecular activation of C-H bonds in transition-metal complexes. Chem. Rev. 1990, 90:403-424.
-
(1990)
Chem. Rev.
, vol.90
, pp. 403-424
-
-
Ryabov, A.D.1
-
23
-
-
33750731982
-
Carbene vs olefin products of C-H activation on ruthenium via competing alpha- and beta-H elimination
-
Kuznetsov V.F., Abdur-Rashid K., Lough A.J., Gusev D.G. Carbene vs olefin products of C-H activation on ruthenium via competing alpha- and beta-H elimination. J. Am. Chem. Soc. 2006, 128:14388-14396.
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14388-14396
-
-
Kuznetsov, V.F.1
Abdur-Rashid, K.2
Lough, A.J.3
Gusev, D.G.4
-
24
-
-
0141923586
-
Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C-H functionalization
-
Hennessy E.J., Buchwald S.L. Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C-H functionalization. J. Am. Chem. Soc. 2003, 125:12084-12085.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 12084-12085
-
-
Hennessy, E.J.1
Buchwald, S.L.2
-
25
-
-
0030599267
-
On the mechanism of cine substitution in the Stille reaction: new evidence for the intermediacy of Pd(0) carbenes
-
Farina V., Hossain M.A. On the mechanism of cine substitution in the Stille reaction: new evidence for the intermediacy of Pd(0) carbenes. Tetrahedron Lett. 1996, 37:6997-7000.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 6997-7000
-
-
Farina, V.1
Hossain, M.A.2
-
26
-
-
33751157148
-
The anomalous Stille reactions of methyl alpha-(tributylstannyl)acrylate - evidence for a palladium carbene intermediate
-
Busacca C.A., Swestock J., Johnson R.E., Bailey T.R., Musza L., Rodger C.A. The anomalous Stille reactions of methyl alpha-(tributylstannyl)acrylate - evidence for a palladium carbene intermediate. J. Org. Chem. 1994, 59:7553-7556.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 7553-7556
-
-
Busacca, C.A.1
Swestock, J.2
Johnson, R.E.3
Bailey, T.R.4
Musza, L.5
Rodger, C.A.6
-
27
-
-
0001549837
-
Novel palladium-catalyzed reactions of propargyl carbonates with carbonucleophiles under neutral conditions
-
Tsuji J., Watanabe H., Minami I., Shimizu I. Novel palladium-catalyzed reactions of propargyl carbonates with carbonucleophiles under neutral conditions. J. Am. Chem. Soc. 1985, 107:2196-2198.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 2196-2198
-
-
Tsuji, J.1
Watanabe, H.2
Minami, I.3
Shimizu, I.4
-
28
-
-
14844318023
-
Discovery of and mechanistic insight into a ligand-modulated palladium-catalyzed Wacker oxidation of styrenes using TBHP
-
Cornell C.N., Sigman M.S. Discovery of and mechanistic insight into a ligand-modulated palladium-catalyzed Wacker oxidation of styrenes using TBHP. J. Am. Chem. Soc. 2005, 127:2796-2797.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2796-2797
-
-
Cornell, C.N.1
Sigman, M.S.2
-
29
-
-
0035979069
-
Regioselective palladium-catalyzed arylation of 2-furaldehyde
-
McClure M.S., Glover B., McSorley E., Millar A., Osterhout M.H., Roschangar F. Regioselective palladium-catalyzed arylation of 2-furaldehyde. Org. Lett. 2001, 3:1677-1680.
-
(2001)
Org. Lett.
, vol.3
, pp. 1677-1680
-
-
McClure, M.S.1
Glover, B.2
McSorley, E.3
Millar, A.4
Osterhout, M.H.5
Roschangar, F.6
-
30
-
-
0142132016
-
Competing regiochemical pathways in the Heck arylation of 1,2-dihydronaphthalene
-
Maeda K., Farrington E.J., Galardon E., John B.D., Brown J.M. Competing regiochemical pathways in the Heck arylation of 1,2-dihydronaphthalene. Adv. Synth. Catal. 2002, 344:104-109.
-
(2002)
Adv. Synth. Catal.
, vol.344
, pp. 104-109
-
-
Maeda, K.1
Farrington, E.J.2
Galardon, E.3
John, B.D.4
Brown, J.M.5
-
31
-
-
0000793787
-
On the nature of the catalytic palladium-mediated elimination of allylic carbonates and acetates to form 1,3-dienes
-
Takacs J.M., Lawson E.C., Clement F. On the nature of the catalytic palladium-mediated elimination of allylic carbonates and acetates to form 1,3-dienes. J. Am. Chem. Soc. 1997, 119:5956-5957.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 5956-5957
-
-
Takacs, J.M.1
Lawson, E.C.2
Clement, F.3
-
32
-
-
0001791627
-
Mechanism of the palladium-catalyzed elimination of acetic-acid from allylic acetates
-
Andersson P.G., Schab S. Mechanism of the palladium-catalyzed elimination of acetic-acid from allylic acetates. Organometallics 1995, 14:1-2.
-
(1995)
Organometallics
, vol.14
, pp. 1-2
-
-
Andersson, P.G.1
Schab, S.2
-
33
-
-
0032516334
-
The Heck olefination reaction; a DFT study of the elimination pathway
-
Deeth R.J., Smith A., Hii K.K., Brown J.M. The Heck olefination reaction; a DFT study of the elimination pathway. Tetrahedron Lett. 1998, 39:3229-3232.
-
(1998)
Tetrahedron Lett.
, vol.39
, pp. 3229-3232
-
-
Deeth, R.J.1
Smith, A.2
Hii, K.K.3
Brown, J.M.4
-
34
-
-
77952905785
-
Heck-type reactions of imine derivatives: a DFT study
-
Li Z., Fu Y., Zhang S.L., Guo Q.X., Liu L. Heck-type reactions of imine derivatives: a DFT study. Chem. Asian J. 2010, 5:1475-1486.
-
(2010)
Chem. Asian J.
, vol.5
, pp. 1475-1486
-
-
Li, Z.1
Fu, Y.2
Zhang, S.L.3
Guo, Q.X.4
Liu, L.5
-
35
-
-
83755169020
-
Theoretical analysis of the mechanism of palladium(II) acetate-catalyzed oxidative heck coupling of electron-deficient arenes with alkenes: effects of the pyridine-type ancillary ligand and origins of the meta-regioselectivity
-
Zhang S.L., Shi L., Ding Y.Q. Theoretical analysis of the mechanism of palladium(II) acetate-catalyzed oxidative heck coupling of electron-deficient arenes with alkenes: effects of the pyridine-type ancillary ligand and origins of the meta-regioselectivity. J. Am. Chem. Soc. 2011, 133:20218-20229.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 20218-20229
-
-
Zhang, S.L.1
Shi, L.2
Ding, Y.Q.3
-
36
-
-
2442609566
-
Comparing nickel- and palladium-catalyzed Heck reactions
-
Lin B.L., Liu L., Fu Y., Luo S.W., Chen Q., Guo Q.X. Comparing nickel- and palladium-catalyzed Heck reactions. Organometallics 2004, 23:2114-2123.
-
(2004)
Organometallics
, vol.23
, pp. 2114-2123
-
-
Lin, B.L.1
Liu, L.2
Fu, Y.3
Luo, S.W.4
Chen, Q.5
Guo, Q.X.6
-
41
-
-
0345491105
-
Development of the Colle-Salvetti correlation-energy formula into a functional of the electron-density
-
Lee C.T., Yang W.T., Parr R.G. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron-density. Phys. Rev. B 1988, 37:785-789.
-
(1988)
Phys. Rev. B
, vol.37
, pp. 785-789
-
-
Lee, C.T.1
Yang, W.T.2
Parr, R.G.3
-
42
-
-
27344448074
-
Abinitio effective core potentials for molecular calculations - potentials for K-Au including the outermost core orbitals
-
lanl2dz: D95V (Dunning/Huzinaga valence double-zeta) on the first row, los Alamos ECP plus DZ on Na-La, Hf-Bi. See
-
Hay P.J., Wadt W.R. Abinitio effective core potentials for molecular calculations - potentials for K-Au including the outermost core orbitals. J. Chem. Phys. 1985, 82:299-310. lanl2dz: D95V (Dunning/Huzinaga valence double-zeta) on the first row, los Alamos ECP plus DZ on Na-La, Hf-Bi. See.
-
(1985)
J. Chem. Phys.
, vol.82
, pp. 299-310
-
-
Hay, P.J.1
Wadt, W.R.2
-
43
-
-
0009803110
-
Ab initio energy-adjusted pseudopotentials for the noble gases Ne through Xe: calculation of atomic dipole and quadruple polarizabilities
-
(SDD: D95 (Dunning/Huzinaga full double zeta) up to Ar and Stuttgart/Dresden ECPs on the remainder of the periodic table. See:)
-
Nicklass A., Dolg M., Stoll H., Preuss H. Ab initio energy-adjusted pseudopotentials for the noble gases Ne through Xe: calculation of atomic dipole and quadruple polarizabilities. J. Chem. Phys. 1995, 102:8942-8952. (SDD: D95 (Dunning/Huzinaga full double zeta) up to Ar and Stuttgart/Dresden ECPs on the remainder of the periodic table. See:).
-
(1995)
J. Chem. Phys.
, vol.102
, pp. 8942-8952
-
-
Nicklass, A.1
Dolg, M.2
Stoll, H.3
Preuss, H.4
-
44
-
-
79953033547
-
Pd-catalyzed carbonylation of diazo compounds at atmospheric pressure: a catalytic approach to ketenes
-
Zhang Z., Liu Y., Ling L., Li Y., Dong Y., Gong M., Zhao X., Zhang Y., Wang J. Pd-catalyzed carbonylation of diazo compounds at atmospheric pressure: a catalytic approach to ketenes. J. Am. Chem. Soc. 2011, 133:4330-4341.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 4330-4341
-
-
Zhang, Z.1
Liu, Y.2
Ling, L.3
Li, Y.4
Dong, Y.5
Gong, M.6
Zhao, X.7
Zhang, Y.8
Wang, J.9
-
45
-
-
84863012615
-
Key mechanistic features of enantioselective C-H bond activation reactions catalyzed by [(chiral mono-N-protected amino acid) - Pd(II)] complexes
-
Musaev D.G., Kaledin A., Shi B.-F., Yu J.-Q. Key mechanistic features of enantioselective C-H bond activation reactions catalyzed by [(chiral mono-N-protected amino acid) - Pd(II)] complexes. J. Am. Chem. Soc. 2011, 134:1690-1698.
-
(2011)
J. Am. Chem. Soc.
, vol.134
, pp. 1690-1698
-
-
Musaev, D.G.1
Kaledin, A.2
Shi, B.-F.3
Yu, J.-Q.4
-
46
-
-
79953066394
-
Controlling site selectivity in pd-catalyzed oxidative cross-coupling reactions
-
Lyons T.W., Hull K.L., Sanford M.S. Controlling site selectivity in pd-catalyzed oxidative cross-coupling reactions. J. Am. Chem. Soc. 2011, 133:4455-4464.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 4455-4464
-
-
Lyons, T.W.1
Hull, K.L.2
Sanford, M.S.3
-
47
-
-
80052565196
-
Chemo- and regioselectivity-tunable Pd-catalyzed allylic alkylation of imines
-
Chen J.-P., Peng Q., Lei B.-L., Hou X.-L., Wu Y.-D. Chemo- and regioselectivity-tunable Pd-catalyzed allylic alkylation of imines. J. Am. Chem. Soc. 2011, 133:14180-14183.
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 14180-14183
-
-
Chen, J.-P.1
Peng, Q.2
Lei, B.-L.3
Hou, X.-L.4
Wu, Y.-D.5
-
48
-
-
77958057083
-
Palladium-catalyzed decarboxylative couplings of 2-(2-azaaryl)acetates with aryl halides and triflates
-
Shang R., Yang Z.-W., Wang Y., Zhang S.-L., Liu L. Palladium-catalyzed decarboxylative couplings of 2-(2-azaaryl)acetates with aryl halides and triflates. J. Am. Chem. Soc. 2010, 132:14391-14393.
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 14391-14393
-
-
Shang, R.1
Yang, Z.-W.2
Wang, Y.3
Zhang, S.-L.4
Liu, L.5
-
49
-
-
69949117215
-
Synthesis of aromatic esters via Pd-catalyzed decarboxylative coupling of potassium oxalate monoesters with aryl bromides and chlorides
-
Shang R., Fu Y., Li J.-B., Zhang S.-L., Guo Q.-X., Liu L. Synthesis of aromatic esters via Pd-catalyzed decarboxylative coupling of potassium oxalate monoesters with aryl bromides and chlorides. J. Am. Chem. Soc. 2009, 131:5738-5739.
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5738-5739
-
-
Shang, R.1
Fu, Y.2
Li, J.-B.3
Zhang, S.-L.4
Guo, Q.-X.5
Liu, L.6
-
50
-
-
51049108168
-
Theoretical study on monoligated Pd-catalyzed cross-coupling reactions of aryl chlorides and bromides
-
Li Z., Fu Y., Guo Q.-X., Liu L. Theoretical study on monoligated Pd-catalyzed cross-coupling reactions of aryl chlorides and bromides. Organometallics 2008, 27:4043-4049.
-
(2008)
Organometallics
, vol.27
, pp. 4043-4049
-
-
Li, Z.1
Fu, Y.2
Guo, Q.-X.3
Liu, L.4
-
51
-
-
50549090818
-
Mechanism for carbon-oxygen bond-forming reductive elimination from palladium(IV) complexes
-
Fu Y., Li Z., Liang S., Guo Q.-X., Liu L. Mechanism for carbon-oxygen bond-forming reductive elimination from palladium(IV) complexes. Organometallics 2008, 27:3736-3742.
-
(2008)
Organometallics
, vol.27
, pp. 3736-3742
-
-
Fu, Y.1
Li, Z.2
Liang, S.3
Guo, Q.-X.4
Liu, L.5
-
52
-
-
84869080914
-
Mechanism of palladium-catalyzed decarboxylation cross-coupling between cyanoacetate salts and aryl halides
-
Jiang Y.-Y., Fu Y., Liu L. Mechanism of palladium-catalyzed decarboxylation cross-coupling between cyanoacetate salts and aryl halides. Sci. China Chem. 2012, 55:2057-2062.
-
(2012)
Sci. China Chem.
, vol.55
, pp. 2057-2062
-
-
Jiang, Y.-Y.1
Fu, Y.2
Liu, L.3
-
53
-
-
33751044609
-
The path of chemical-reactions - the Irc approach
-
Fukui K. The path of chemical-reactions - the Irc approach. Acc. Chem. Res. 1981, 14:363-368.
-
(1981)
Acc. Chem. Res.
, vol.14
, pp. 363-368
-
-
Fukui, K.1
-
54
-
-
36549095692
-
An improved algorithm for reaction-path following
-
Gonzalez C., Schlegel H.B. An improved algorithm for reaction-path following. J. Chem. Phys. 1989, 90:2154-2161.
-
(1989)
J. Chem. Phys.
, vol.90
, pp. 2154-2161
-
-
Gonzalez, C.1
Schlegel, H.B.2
-
55
-
-
40549127108
-
Density functionals with broad applicability in chemistry
-
Zhao Y., Truhlar D.G. Density functionals with broad applicability in chemistry. Acc. Chem. Res. 2008, 41:157-167.
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 157-167
-
-
Zhao, Y.1
Truhlar, D.G.2
-
56
-
-
66349120487
-
Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions
-
Cramer C.J., Marenich A.V., Truhlar D.G. Universal solvation model based on solute electron density and on a continuum model of the solvent defined by the bulk dielectric constant and atomic surface tensions. J. Phys. Chem. B 2009, 113:6378-6396.
-
(2009)
J. Phys. Chem. B
, vol.113
, pp. 6378-6396
-
-
Cramer, C.J.1
Marenich, A.V.2
Truhlar, D.G.3
-
57
-
-
84872185058
-
-
Gaussian, Inc., Wallingford CT, Gaussian 09, Revision B.1
-
Gaussian 09, Revision B.1, M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G.A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H.P. Hratchian, A.F. Izmaylov, J. Bloino, G. Zheng, J.L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J.A. Montgomery Jr., J.E. Peralta, F. Ogliaro, M. Bearpark, J.J. Heyd, E. Brothers, K.N. Kudin, V.N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J.M. Millam, M. Klene, J.E. Knox, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, R.L. Martin, K. Morokuma, V.G. Zakrzewski, G.A. Voth, P. Salvador, J.J. Dannenberg, S. Dapprich, A.D. Daniels, Ö. Farkas, J.B. Foresman, J.V. Ortiz, J. Cioslowski, D.J. Fox, Gaussian, Inc., Wallingford CT, 2009.
-
(2009)
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Scalmani, G.7
Barone, V.8
Mennucci, B.9
Petersson, G.A.10
Nakatsuji, H.11
Caricato, M.12
Li, X.13
Hratchian, H.P.14
Izmaylov, A.F.15
Bloino, J.16
Zheng, G.17
Sonnenberg, J.L.18
Hada, M.19
Ehara, M.20
Toyota, K.21
Fukuda, R.22
Hasegawa, J.23
Ishida, M.24
Nakajima, T.25
Honda, Y.26
Kitao, O.27
Nakai, H.28
Vreven, T.29
Montgomery Jr., J.A.30
Peralta, J.E.31
Ogliaro, F.32
Bearpark, M.33
Heyd, J.J.34
Brothers, E.35
Kudin, K.N.36
Staroverov, V.N.37
Kobayashi, R.38
Normand, J.39
Raghavachari, K.40
Rendell, A.41
Burant, J.C.42
Iyengar, S.S.43
Tomasi, J.44
Cossi, M.45
Rega, N.46
Millam, J.M.47
Klene, M.48
Knox, J.E.49
Cross, J.B.50
Bakken, V.51
Adamo, C.52
Jaramillo, J.53
Gomperts, R.54
Stratmann, R.E.55
Yazyev, O.56
Austin, A.J.57
Cammi, R.58
Pomelli, C.59
Ochterski, J.W.60
Martin, R.L.61
Morokuma, K.62
Zakrzewski, V.G.63
Voth, G.A.64
Salvador, P.65
Dannenberg, J.J.66
Dapprich, S.67
Daniels, A.D.68
Farkas, O.69
Foresman, J.B.70
Ortiz, J.V.71
Cioslowski, J.72
Fox, D.J.73
more..
|