-
1
-
-
57549097483
-
-
For reviews, see: (a) de Meijere, A, Diederich, F, Eds, 2nd ed, Wiley-VCH: Weinheim, Germany
-
For reviews, see: (a) de Meijere, A., Diederich, F., Eds. Metal-Catalyzed Cross-Coupling Reactions, 2nd ed.; Wiley-VCH: Weinheim, Germany, 2004.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
-
-
-
2
-
-
30944453545
-
-
Negishi, E, Ed, Wiley-Interscience: New York
-
(b) Handbook of Organopalladium Chemistry, Negishi, E., Ed.; Wiley-Interscience: New York, 2002.
-
(2002)
Handbook of Organopalladium Chemistry
-
-
-
3
-
-
37049127647
-
Activation of Grignard Reagents by Transition-Metal Complexes. A New and Simple Synthesis of Trans-Stilbenes and Polyphenyls
-
(a) Corriu, R. J. P.; Massé, J. P. Activation of Grignard Reagents by Transition-Metal Complexes. A New and Simple Synthesis of Trans-Stilbenes and Polyphenyls. J. Chem. Soc., Chem. Commun. 1972, 144a.
-
(1972)
J. Chem. Soc., Chem. Commun
-
-
Corriu, R.J.P.1
Massé, J.P.2
-
4
-
-
33947091124
-
-
Tamao, K.; Sumitani, K.; Kumada, M. Selective Carbon-Carbon Bond Formation by Cross-Coupling of Grignard Reagents with Organic Halides. Catalysis by Nickel-Phosphine Complexes. J. Am. Chem. Soc. 1972, 94, 4374-4376.
-
(b) Tamao, K.; Sumitani, K.; Kumada, M. Selective Carbon-Carbon Bond Formation by Cross-Coupling of Grignard Reagents with Organic Halides. Catalysis by Nickel-Phosphine Complexes. J. Am. Chem. Soc. 1972, 94, 4374-4376.
-
-
-
-
5
-
-
0000390817
-
Organosilicon Compounds in Cross-coupling Reactions
-
For reviews on silicon-based cross-coupling, see: a, Diederich, F, Stang, P. J, Eds, Wiley-VCH: Weinheim, Germany, Chapter 10
-
For reviews on silicon-based cross-coupling, see: (a) Hiyama, T. Organosilicon Compounds in Cross-coupling Reactions. In Metal-Catalyzed Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1998; Chapter 10.
-
(1998)
Metal-Catalyzed Cross-Coupling Reactions
-
-
Hiyama, T.1
-
6
-
-
12344286607
-
Organosilicon Compounds in Cross-Coupling Reactions
-
de Meijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim, Germany, Chapter 4
-
(b) Denmark, S. E.; Sweis, R. F. Organosilicon Compounds in Cross-Coupling Reactions. In Metal-Catalyzed Cross-Coupling Reactions; de Meijere, A., Diederich, F., Eds.; Wiley-VCH: Weinheim, Germany, 2004; Vol. 1, Chapter 4.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
, vol.1
-
-
Denmark, S.E.1
Sweis, R.F.2
-
7
-
-
10044220360
-
Recent Advances in Group 14 Cross-Coupling: Si and Ge-Based Alternatives to the Stille Reaction
-
(c) Spivey, A. C.; Gripton, C. J. G.; Hannah, J. P. Recent Advances in Group 14 Cross-Coupling: Si and Ge-Based Alternatives to the Stille Reaction. Curr. Org. Synth. 2004, 1, 211-226.
-
(2004)
Curr. Org. Synth
, vol.1
, pp. 211-226
-
-
Spivey, A.C.1
Gripton, C.J.G.2
Hannah, J.P.3
-
8
-
-
33845558052
-
Bond Dissociation Energy Values in Silicon-Containing Compounds and Some of Their Implications
-
Walsh, R. Bond Dissociation Energy Values in Silicon-Containing Compounds and Some of Their Implications. Acc. Chem. Res. 1981, 14, 246-252.
-
(1981)
Acc. Chem. Res
, vol.14
, pp. 246-252
-
-
Walsh, R.1
-
9
-
-
0001220792
-
Preparation and NMR Studies of Pentacoordinated Silicon Anions
-
Damrauer, R.; Danahey, S. E. Preparation and NMR Studies of Pentacoordinated Silicon Anions. Organometallics 1986, 5, 1490-1494.
-
(1986)
Organometallics
, vol.5
, pp. 1490-1494
-
-
Damrauer, R.1
Danahey, S.E.2
-
10
-
-
33845277870
-
Cross-Coupling of Organosilanes with Organic Halides Mediated by Palladium Catalyst and Tris(diethylamino)sulfonium Difluorotrimethylsilicate
-
Hatanaka, Y.; Hiyama, T. Cross-Coupling of Organosilanes with Organic Halides Mediated by Palladium Catalyst and Tris(diethylamino)sulfonium Difluorotrimethylsilicate. J. Org. Chem. 1988, 53, 918-920.
-
(1988)
J. Org. Chem
, vol.53
, pp. 918-920
-
-
Hatanaka, Y.1
Hiyama, T.2
-
11
-
-
0034068081
-
Substituent Effect of 3,3,3-Trifluoropropyl Group on Organic Silanols. Palladium-Mediated Mizoroki-Heck Type and Cross-Coupling Reactions
-
For other examples of silicon-based cross-coupling, see: a
-
For other examples of silicon-based cross-coupling, see: (a) Hirabayashi, K.; Kondo, T.; Toriyama, F.; Nishihara, Y.; Mori, A. Substituent Effect of 3,3,3-Trifluoropropyl Group on Organic Silanols. Palladium-Mediated Mizoroki-Heck Type and Cross-Coupling Reactions. Bull. Chem. Soc. Jpn. 2000, 73, 749-750.
-
(2000)
Bull. Chem. Soc. Jpn
, vol.73
, pp. 749-750
-
-
Hirabayashi, K.1
Kondo, T.2
Toriyama, F.3
Nishihara, Y.4
Mori, A.5
-
12
-
-
0042760394
-
Efficient Cross-Coupling Reactions of Aryl Chlorides and Bromides with Phenyl- or Vinyltrimethoxysilane Mediated by a Palladium/Imidazolium Chloride System
-
(b) Lee, H. M.; Nolan, S. P. Efficient Cross-Coupling Reactions of Aryl Chlorides and Bromides with Phenyl- or Vinyltrimethoxysilane Mediated by a Palladium/Imidazolium Chloride System. Org. Lett. 2000, 2, 2053-2055.
-
(2000)
Org. Lett
, vol.2
, pp. 2053-2055
-
-
Lee, H.M.1
Nolan, S.P.2
-
13
-
-
1542397449
-
Preparation of Functionalized Biaryl Compounds via Cross-coupling Reactions of Aryltrialkoxysilanes with Aryl Bromides
-
(c) Shibata, K.; Miyazawa, K.; Goto, Y. Preparation of Functionalized Biaryl Compounds via Cross-coupling Reactions of Aryltrialkoxysilanes with Aryl Bromides. Chem. Commun. 1997, 1309-1310.
-
(1997)
Chem. Commun
, pp. 1309-1310
-
-
Shibata, K.1
Miyazawa, K.2
Goto, Y.3
-
14
-
-
28444476172
-
Recent Advances in Siloxane-Based Aryl-Aryl Coupling Reactions: Focus on Heteroaromatic Systems
-
(d) Handy, C. J.; Manoso, A. S.; McElroy, W. T.; Seganish, W. M.; DeShong, P. Recent Advances in Siloxane-Based Aryl-Aryl Coupling Reactions: Focus on Heteroaromatic Systems. Tetrahedron 2005, 61, 12201-12225.
-
(2005)
Tetrahedron
, vol.61
, pp. 12201-12225
-
-
Handy, C.J.1
Manoso, A.S.2
McElroy, W.T.3
Seganish, W.M.4
DeShong, P.5
-
15
-
-
0034820257
-
Palladium-Catalyzed Cross-Coupling Reaction of Alkenyldimethyl(2-pyridyl)silanes with Organic Halides: Complete Switch from the Carbometalation Pathway to the Transmetalation Pathway
-
(a) Itami, K.; Nokami, T.; Yoshida, J. Palladium-Catalyzed Cross-Coupling Reaction of Alkenyldimethyl(2-pyridyl)silanes with Organic Halides: Complete Switch from the Carbometalation Pathway to the Transmetalation Pathway. J. Am. Chem. Soc. 2001, 123, 5600-5601.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 5600-5601
-
-
Itami, K.1
Nokami, T.2
Yoshida, J.3
-
16
-
-
0036003102
-
Alkenyldimethyl(2-thienyl)silanes, Excellent Coupling Partner for the Palladium-Catalyzed Cross-Coupling Reaction
-
(b) Hosoi, K.; Nozaki, K.; Hiyama, T. Alkenyldimethyl(2-thienyl)silanes, Excellent Coupling Partner for the Palladium-Catalyzed Cross-Coupling Reaction. Chem. Lett. 2002, 138-139.
-
(2002)
Chem. Lett
, pp. 138-139
-
-
Hosoi, K.1
Nozaki, K.2
Hiyama, T.3
-
17
-
-
0041851126
-
Ruthenium-Catalyzed Vinylsilane Synthesis and Cross-Coupling as a Selective Approach to Alkenes: Benzyldimethylsilyl as a Robust Vinylmetal Functionality
-
(c) Trost, B. M.; Machacek, M. R.; Ball, Z. T. Ruthenium-Catalyzed Vinylsilane Synthesis and Cross-Coupling as a Selective Approach to Alkenes: Benzyldimethylsilyl as a Robust Vinylmetal Functionality. Org. Lett. 2003, 5, 1895-1898.
-
(2003)
Org. Lett
, vol.5
, pp. 1895-1898
-
-
Trost, B.M.1
Machacek, M.R.2
Ball, Z.T.3
-
18
-
-
0344299286
-
Highly Stereospecific Cross-Coupling of Alkenylsilacyclobutanes
-
(a) Denmark, S. E.; Choi, J. Y. Highly Stereospecific Cross-Coupling of Alkenylsilacyclobutanes. J. Am. Chem. Soc. 1999, 121, 5821-5822.
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 5821-5822
-
-
Denmark, S.E.1
Choi, J.Y.2
-
19
-
-
0000198109
-
Convergence of Mechanistic Pathways in the Palladium(0)-Catalyzed Cross-Coupling of Alkenylsilacyclobutanes and Alkenylsilanols
-
(b) Denmark, S. E.; Wehrli, D.; Choi, J. Y. Convergence of Mechanistic Pathways in the Palladium(0)-Catalyzed Cross-Coupling of Alkenylsilacyclobutanes and Alkenylsilanols. Org. Lett. 2000, 2, 2491-2494.
-
(2000)
Org. Lett
, vol.2
, pp. 2491-2494
-
-
Denmark, S.E.1
Wehrli, D.2
Choi, J.Y.3
-
20
-
-
1842862944
-
Fluoride-Promoted Cross-Coupling Reactions of Alkenylsilanols. Elucidation of the Mechanism through Spectroscopic and Kinetic Analysis
-
Denmark, S. E.; Sweis, R. F.; Wehrli, D. Fluoride-Promoted Cross-Coupling Reactions of Alkenylsilanols. Elucidation of the Mechanism through Spectroscopic and Kinetic Analysis. J. Am. Chem. Soc. 2004, 126, 4865-4875.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4865-4875
-
-
Denmark, S.E.1
Sweis, R.F.2
Wehrli, D.3
-
21
-
-
1842843364
-
Cross-Coupling Reactions of Organosilicon Compounds: New Concepts and Recent Advances
-
(a) Denmark, S. E.; Sweis, R. F. Cross-Coupling Reactions of Organosilicon Compounds: New Concepts and Recent Advances. Chem. Pharm. Bull. 2002, 50, 1531-1541.
-
(2002)
Chem. Pharm. Bull
, vol.50
, pp. 1531-1541
-
-
Denmark, S.E.1
Sweis, R.F.2
-
22
-
-
0036798587
-
Design and Implementation of New, Silicon-Based, Cross Coupling Reactions: Importance of Silicon-Oxygen Bonds
-
(b) Denmark, S. E.; Sweis, R. F. Design and Implementation of New, Silicon-Based, Cross Coupling Reactions: Importance of Silicon-Oxygen Bonds. Acc. Chem. Res. 2002, 35, 835-846.
-
(2002)
Acc. Chem. Res
, vol.35
, pp. 835-846
-
-
Denmark, S.E.1
Sweis, R.F.2
-
23
-
-
1342311661
-
Organosilicon Reagents: Synthesis and Application to Palladium-Catalyzed Cross-Coupling Reactions
-
(c) Denmark, S. E.; Ober, M. H. Organosilicon Reagents: Synthesis and Application to Palladium-Catalyzed Cross-Coupling Reactions. Aldrichim. Acta 2003, 36, 75-85.
-
(2003)
Aldrichim. Acta
, vol.36
, pp. 75-85
-
-
Denmark, S.E.1
Ober, M.H.2
-
24
-
-
33745686514
-
Palladium-Catalyzed Cross-Coupling Reactions of Silanolates: A Paradigm Shift in Silicon-Based Cross-Coupling Reactions
-
(d) Denmark, S. E.; Baird, J. D. Palladium-Catalyzed Cross-Coupling Reactions of Silanolates: A Paradigm Shift in Silicon-Based Cross-Coupling Reactions. Chem. - Eur. J. 2006, 12, 4954-4963.
-
(2006)
Chem. - Eur. J
, vol.12
, pp. 4954-4963
-
-
Denmark, S.E.1
Baird, J.D.2
-
25
-
-
0034811829
-
Fluoride-Free Cross-Coupling of Organosilanols
-
Denmark, S. E.; Sweis, R. F. Fluoride-Free Cross-Coupling of Organosilanols. J. Am. Chem. Soc. 2001, 123, 6439-6440.
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 6439-6440
-
-
Denmark, S.E.1
Sweis, R.F.2
-
26
-
-
20544450502
-
Mechanistic Aspects of Metal-Catalyzed C, C-and C, X-Bond Forming Reactions
-
2nd Ed, de Meijere, A, Diederich, F, Eds, Wiley-VCH: Weinheim, Germany, Chapter 1
-
Echavarren, A. M.; Cardenas, D. J. Mechanistic Aspects of Metal-Catalyzed C, C-and C, X-Bond Forming Reactions. In Metal-Catalyzed Cross-Coupling Reactions, 2nd Ed.; de Meijere, A., Diederich, F., Eds.; Wiley-VCH: Weinheim, Germany, 2004; Vol. 1, Chapter 1.
-
(2004)
Metal-Catalyzed Cross-Coupling Reactions
, vol.1
-
-
Echavarren, A.M.1
Cardenas, D.J.2
-
27
-
-
4644245555
-
The Mechanism of the Stille Reaction
-
Espinet, P.; Echavarren, A. M. The Mechanism of the Stille Reaction. Angew. Chem., Int. Ed. 2004, 43, 4704-4734.
-
(2004)
Angew. Chem., Int. Ed
, vol.43
, pp. 4704-4734
-
-
Espinet, P.1
Echavarren, A.M.2
-
28
-
-
33750464872
-
-
Denmark, S. E.; Neuville, L.; Christy, M. E. L.; Tymonko, S. A. A Qualitative Examination of the Effects of Silicon Substituents on the Efficiency of Cross-Coupling Reactions. J. Org. Chem. 2006, 71, 8500-8509.
-
Denmark, S. E.; Neuville, L.; Christy, M. E. L.; Tymonko, S. A. A Qualitative Examination of the Effects of Silicon Substituents on the Efficiency of Cross-Coupling Reactions. J. Org. Chem. 2006, 71, 8500-8509.
-
-
-
-
29
-
-
1842862941
-
Cross-Coupling Reactions of Alkenylsilanolates. Investigation of the Mechanism and Identification of Key Intermediates through Kinetic Analysis
-
Denmark, S. E.; Sweis, R. F. Cross-Coupling Reactions of Alkenylsilanolates. Investigation of the Mechanism and Identification of Key Intermediates through Kinetic Analysis. J. Am. Chem. Soc. 2004, 126, 4876-4882.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4876-4882
-
-
Denmark, S.E.1
Sweis, R.F.2
-
30
-
-
57549109306
-
-
Although the kinetic experiments were performed for 2-iodothiophene to facilitate the kinetic analysis, we believe that this scheme is general for coupling of all aromatic halides. Moreover, this picture allows a clearer insight into how the turnover-limiting step can change with structure
-
Although the kinetic experiments were performed for 2-iodothiophene (to facilitate the kinetic analysis), we believe that this scheme is general for coupling of all aromatic halides. Moreover, this picture allows a clearer insight into how the turnover-limiting step can change with structure.
-
-
-
-
31
-
-
0037925363
-
Cross-Coupling Reactions of Arylsilanols with Substituted Aryl Halide
-
(a) Denmark, S. E.; Ober, M. H. Cross-Coupling Reactions of Arylsilanols with Substituted Aryl Halide. Org. Lett. 2003, 5, 1357-1360.
-
(2003)
Org. Lett
, vol.5
, pp. 1357-1360
-
-
Denmark, S.E.1
Ober, M.H.2
-
32
-
-
12344293447
-
Palladium-Catalyzed Cross-Coupling Reactions of Substituted Aryl(dimethyl)silanols
-
(b) Denmark, S. E.; Ober, M. H. Palladium-Catalyzed Cross-Coupling Reactions of Substituted Aryl(dimethyl)silanols. Adv. Synth. Catal. 2004, 346, 1703-1714.
-
(2004)
Adv. Synth. Catal
, vol.346
, pp. 1703-1714
-
-
Denmark, S.E.1
Ober, M.H.2
-
33
-
-
57549106873
-
-
Denmark, S. E.; Tymonko, S. A.; Smith, R. C.; Ober, M. H. Palladium-Catalyzed Cross-Coupling Reactions of Alkenyl- and Aryl(dimethyl)silanolates Proceed via Neutral (8-Si-4) Arylpalladium Silanolate Complexes. J. Am. Chem. Soc. Manuscript submitted for publication.
-
Denmark, S. E.; Tymonko, S. A.; Smith, R. C.; Ober, M. H. Palladium-Catalyzed Cross-Coupling Reactions of Alkenyl- and Aryl(dimethyl)silanolates Proceed via Neutral (8-Si-4) Arylpalladium Silanolate Complexes. J. Am. Chem. Soc. Manuscript submitted for publication.
-
-
-
-
34
-
-
33747058703
-
Palladium Catalyzed Cross-Coupling of (Z)-1-Heptenyldimethylsilanol with 4-iodoanisole: (Z)-1-Heptenyl- 4-methoxybenzene
-
Denmark, S. E.; Wang, Z. Palladium Catalyzed Cross-Coupling of (Z)-1-Heptenyldimethylsilanol with 4-iodoanisole: (Z)-1-Heptenyl- 4-methoxybenzene. Org. Synth. 2004, 81, 42-53.
-
(2004)
Org. Synth
, vol.81
, pp. 42-53
-
-
Denmark, S.E.1
Wang, Z.2
-
35
-
-
0003799267
-
-
Stang, P. J, Diederich, F. Eds, Wiley-VCH; Weinheim, Germany
-
Modern Acetylene Chemistry; Stang, P. J., Diederich, F. Eds.; Wiley-VCH; Weinheim, Germany, 1995.
-
(1995)
Modern Acetylene Chemistry
-
-
-
36
-
-
57549105905
-
-
Sonogashira, K. Cross-Coupling Reactions to sp Carbon Atoms. In Metal-Catalyzed, Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1995; Chapter 5.
-
Sonogashira, K. Cross-Coupling Reactions to sp Carbon Atoms. In Metal-Catalyzed, Cross-Coupling Reactions; Diederich, F., Stang, P. J., Eds.; Wiley-VCH: Weinheim, Germany, 1995; Chapter 5.
-
-
-
-
37
-
-
0037943974
-
Palladium-Catalyzed Alkynylation
-
For a recent review of organometallic reagents in the Sonogashira reaction, see
-
For a recent review of organometallic reagents in the Sonogashira reaction, see: Negishi, E.; Anastasia, L. Palladium-Catalyzed Alkynylation. Chem. Rev. 2003, 103, 1979-2018.
-
(2003)
Chem. Rev
, vol.103
, pp. 1979-2018
-
-
Negishi, E.1
Anastasia, L.2
-
38
-
-
0001587846
-
A One-Pot Synthesis of Conjugated Dienynes by Palladium-Mediated Three Component Cross-Coupling Reaction
-
(a) Hatanaka, Y.; Matsui, K.; Hiyama, T. A One-Pot Synthesis of Conjugated Dienynes by Palladium-Mediated Three Component Cross-Coupling Reaction. Tetrahedron Lett. 1989, 30, 2403-2406.
-
(1989)
Tetrahedron Lett
, vol.30
, pp. 2403-2406
-
-
Hatanaka, Y.1
Matsui, K.2
Hiyama, T.3
-
39
-
-
0034175577
-
Silver Salt-Promoted Direct Cross-Coupling Reactions of Alkynylsilanes with Aryl Iodides: Synthesis of Aryl-Substituted Alkynylamides
-
(b) Koseki, Y.; Omino, K.; Anzai, S.; Nagasaka, T. Silver Salt-Promoted Direct Cross-Coupling Reactions of Alkynylsilanes with Aryl Iodides: Synthesis of Aryl-Substituted Alkynylamides. Tetrahedron Lett. 2000, 41, 2377-2380.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 2377-2380
-
-
Koseki, Y.1
Omino, K.2
Anzai, S.3
Nagasaka, T.4
-
40
-
-
0035211229
-
-
Bertus, P.; Halbes, U.; Pale, P. Pd/Ag-Catalyzed Direct Coupling of 1-Trimethylsilyl Alkynes with Vinyl Triflates. Eur. J. Org. Chem. 2001, 4391-4393.
-
(c) Bertus, P.; Halbes, U.; Pale, P. Pd/Ag-Catalyzed Direct Coupling of 1-Trimethylsilyl Alkynes with Vinyl Triflates. Eur. J. Org. Chem. 2001, 4391-4393.
-
-
-
-
41
-
-
0242408512
-
Cross-Coupling of Alkynylsilanols with Aryl Halides Promoted by Potassium Trimethylsilanolate
-
Denmark, S. E.; Tymonko, S. A. Cross-Coupling of Alkynylsilanols with Aryl Halides Promoted by Potassium Trimethylsilanolate. J. Org. Chem. 2003, 68, 9151-9154.
-
(2003)
J. Org. Chem
, vol.68
, pp. 9151-9154
-
-
Denmark, S.E.1
Tymonko, S.A.2
-
42
-
-
22944454156
-
Synthesis and Functionalization of Indoles through Palladium-Catalyzed Reactions
-
(a) Cacchi, S.; Fabrizi, G. Synthesis and Functionalization of Indoles through Palladium-Catalyzed Reactions. Chem. Rev. 2005, 105, 2873-2920.
-
(2005)
Chem. Rev
, vol.105
, pp. 2873-2920
-
-
Cacchi, S.1
Fabrizi, G.2
-
43
-
-
33746864043
-
Practical Methodologies for the Synthesis of Indoles
-
(b) Humphrey, G. R.; Kuethe, J. T. Practical Methodologies for the Synthesis of Indoles. Chem. Rev. 2006, 106, 2875-2911.
-
(2006)
Chem. Rev
, vol.106
, pp. 2875-2911
-
-
Humphrey, G.R.1
Kuethe, J.T.2
-
44
-
-
39349116935
-
-
Denmark, S. E.; Baird, J. D.; Regens, C. S. Palladium-Catalyzed Cross-Coupling of Five-Membered Heterocyclic Silanolates. J. Org. Chem. 2008, 73, 1440-1455. For the preparation of 18 and 19, see references therein.
-
Denmark, S. E.; Baird, J. D.; Regens, C. S. Palladium-Catalyzed Cross-Coupling of Five-Membered Heterocyclic Silanolates. J. Org. Chem. 2008, 73, 1440-1455. For the preparation of 18 and 19, see references therein.
-
-
-
-
45
-
-
17044382980
-
Synthesis of 3,4,5-Trisubstituted Isoxazoles via Sequential [3 + 2] Cycloaddition/Silicon-Based Cross-Coupling Reactions
-
Denmark, S. E.; Kallemeyn, J. M. Synthesis of 3,4,5-Trisubstituted Isoxazoles via Sequential [3 + 2] Cycloaddition/Silicon-Based Cross-Coupling Reactions. J. Org. Chem. 2005, 70, 2839-2842.
-
(2005)
J. Org. Chem
, vol.70
, pp. 2839-2842
-
-
Denmark, S.E.1
Kallemeyn, J.M.2
-
46
-
-
33947243286
-
Total Synthesis of Papulacandin D
-
Denmark, S. E.; Regens, C. S.; Kobayashi, T. Total Synthesis of Papulacandin D. J. Am. Chem. Soc. 2007, 129, 2774-2776.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 2774-2776
-
-
Denmark, S.E.1
Regens, C.S.2
Kobayashi, T.3
-
47
-
-
20444407705
-
Sequential Cross-Coupling of 1,4-Bissilylbutadienes: Synthesis of Unsymmetrical 1,4-Disubstituted 1,3-Butadienes
-
Denmark, S. E.; Tymonko, S. A. Sequential Cross-Coupling of 1,4-Bissilylbutadienes: Synthesis of Unsymmetrical 1,4-Disubstituted 1,3-Butadienes. J. Am. Chem. Soc. 2005, 127, 8004-8005.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 8004-8005
-
-
Denmark, S.E.1
Tymonko, S.A.2
-
48
-
-
0037112673
-
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
-
Littke, A. F.; Fu, G. C. Palladium-Catalyzed Coupling Reactions of Aryl Chlorides. Angew. Chem., Int. Ed. 2002, 41, 4176-4211.
-
(2002)
Angew. Chem., Int. Ed
, vol.41
, pp. 4176-4211
-
-
Littke, A.F.1
Fu, G.C.2
-
49
-
-
0032560932
-
-
Old, D. W.; Wolfe, J. P.; Buchwald, S. L. A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides. J. Am. Chem. Soc. 1998, 120, 9722-9723.
-
(a) Old, D. W.; Wolfe, J. P.; Buchwald, S. L. A Highly Active Catalyst for Palladium-Catalyzed Cross-Coupling Reactions: Room-Temperature Suzuki Couplings and Amination of Unactivated Aryl Chlorides. J. Am. Chem. Soc. 1998, 120, 9722-9723.
-
-
-
-
50
-
-
0033549832
-
The First General Method for Stille Cross-Couplings of Aryl Chlorides
-
(b) Littke, A. F.; Fu, G. C. The First General Method for Stille Cross-Couplings of Aryl Chlorides. Angew. Chem., Int. Ed. 1999, 38, 2411-2413.
-
(1999)
Angew. Chem., Int. Ed
, vol.38
, pp. 2411-2413
-
-
Littke, A.F.1
Fu, G.C.2
-
51
-
-
0345802559
-
A General Method for the Suzuki-Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-orthosubstituted Biaryls in 2-Propanol at Room Temperature
-
(c) Navarro, O.; Kelly, R. A., III.; Nolan, S. P. A General Method for the Suzuki-Miyaura Cross-Coupling of Sterically Hindered Aryl Chlorides: Synthesis of Di- and Tri-orthosubstituted Biaryls in 2-Propanol at Room Temperature. J. Am. Chem. Soc. 2003, 125, 16194-16195.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 16194-16195
-
-
Navarro, O.1
Kelly III, R.A.2
Nolan, S.P.3
-
52
-
-
9744246801
-
The Development of Palladium Catalysts for C-C and C-Heteroatom bond Forming Reactions of Aryl Chloride Substrates
-
(d) Bedford, R. B.; Cazin, C. S. J.; Holder, D. The Development of Palladium Catalysts for C-C and C-Heteroatom bond Forming Reactions of Aryl Chloride Substrates. Coord. Chem. Rev. 2004, 248, 2283-2321.
-
(2004)
Coord. Chem. Rev
, vol.248
, pp. 2283-2321
-
-
Bedford, R.B.1
Cazin, C.S.J.2
Holder, D.3
-
53
-
-
16844367937
-
Catalysts for Suzuki-Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure
-
Barder, T. E.; Walker, S. D.; Martinelli, J. R.; Buchwald, S. L. Catalysts for Suzuki-Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure. J. Am. Chem. Soc. 2005, 127, 4685-4696.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 4685-4696
-
-
Barder, T.E.1
Walker, S.D.2
Martinelli, J.R.3
Buchwald, S.L.4
-
54
-
-
33845566083
-
-
Denmark, S. E.; Kallemeyn, J. M. Stereospecific Palladium-Catalyzed Cross-Coupling of (E)- and (Z)-Alkenylsilanolates with Aryl Chlorides. J. Am. Chem. Soc. 2006, 128, 15958-15959.
-
Denmark, S. E.; Kallemeyn, J. M. Stereospecific Palladium-Catalyzed Cross-Coupling of (E)- and (Z)-Alkenylsilanolates with Aryl Chlorides. J. Am. Chem. Soc. 2006, 128, 15958-15959.
-
-
-
-
56
-
-
34248634279
-
Phosphine Oxides as Stabilizing Ligands for the Palladium-Catalyzed Cross-Coupling of Potassium Aryldimethylsilanolates
-
The origin of the beneficial effect of phosphine oxides is still not certain. In our current hypothesis, phosphine oxides stabilize palladium(0) nanoparticles and prevent precipitation of palladium black
-
Denmark, S. E.; Smith, R. C.; Tymonko, S. A. Phosphine Oxides as Stabilizing Ligands for the Palladium-Catalyzed Cross-Coupling of Potassium Aryldimethylsilanolates. Tetrahedron 2007, 63, 5730-5738. The origin of the beneficial effect of phosphine oxides is still not certain. In our current hypothesis, phosphine oxides stabilize palladium(0) nanoparticles and prevent precipitation of palladium black.
-
(2007)
Tetrahedron
, vol.63
, pp. 5730-5738
-
-
Denmark, S.E.1
Smith, R.C.2
Tymonko, S.A.3
-
57
-
-
57549113541
-
Cross-Coupling of Substituted Arylsilanolates
-
Manuscript in preparation
-
Denmark, S. E.; Smith, R. C.; Muhuhi, J. M.; Chang, T. Cross-Coupling of Substituted Arylsilanolates. Manuscript in preparation.
-
-
-
Denmark, S.E.1
Smith, R.C.2
Muhuhi, J.M.3
Chang, T.4
-
58
-
-
41449094998
-
A Practical Method for the Vinylation of Aromatic Halides using Inexpensive Organosilicon Reagents
-
(a) Denmark, S. E.; Butler, C. R. A Practical Method for the Vinylation of Aromatic Halides using Inexpensive Organosilicon Reagents. J. Am. Chem. Soc. 2008, 130, 3690-3704.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 3690-3704
-
-
Denmark, S.E.1
Butler, C.R.2
-
59
-
-
57549098833
-
Palladium- (and Nickel-) Catalyzed Vinylation of Aryl Halides
-
in press
-
(b) Denmark, S. E.; Butler, C. R. Palladium- (and Nickel-) Catalyzed Vinylation of Aryl Halides. Chem. Commun. 2008, in press.
-
(2008)
Chem. Commun
-
-
Denmark, S.E.1
Butler, C.R.2
|