-
1
-
-
0003779363
-
-
Beller, M, Bohm, C, Eds, Wiley-VCH: New York
-
(a) Beller, M.; Bohm, C. (Eds.) Transition Metals for Organic Synthesis; Wiley-VCH: New York, 1998; vol. 1.
-
(1998)
Transition Metals for Organic Synthesis
, vol.1
-
-
-
2
-
-
0003397781
-
-
Diedrich, F, Stang, P. J, Eds, Wiley-VCH: Weinheim
-
(b) Diedrich, F.; Stang, P. J., Eds. Metal-Catalyzed Cross-Coupling Reactions; Wiley-VCH: Weinheim, 1998.
-
(1998)
Metal-Catalyzed Cross-Coupling Reactions
-
-
-
3
-
-
0035358840
-
Efficient synthesis of fine chemicals and organic building blocks applying palladium catalyzed coupling reactions
-
(a) Beller, M.; Zapf, A.; Mägerlein, W. Efficient synthesis of fine chemicals and organic building blocks applying palladium catalyzed coupling reactions. Chem. Eng. Technol. 2001, 24, 575-582;
-
(2001)
Chem. Eng. Technol
, vol.24
, pp. 575-582
-
-
Beller, M.1
Zapf, A.2
Mägerlein, W.3
-
4
-
-
0004127585
-
-
Nicolaou, K. C, Hanko, R, Hartwig, W, Eds, Wiley-VCH: Weinheim
-
(b) Nicolaou, K. C.; Hanko, R.; Hartwig, W., Eds. Handbook of Combinatorial Chemistry: Drugs, Catalysts, Materials; Wiley-VCH: Weinheim, 2002.
-
(2002)
Handbook of Combinatorial Chemistry: Drugs, Catalysts, Materials
-
-
-
7
-
-
0003397781
-
-
Diedrich, F, Stang, P. J, Eds, Wiley-VCH: Weinheim
-
(c) Diedrich, F.; Stang, P. J. (Eds). Metal-Catalysed Cross-Coupling Reactions; Wiley-VCH: Weinheim, 1998;
-
(1998)
Metal-Catalysed Cross-Coupling Reactions
-
-
-
9
-
-
33847100088
-
Transition metal-catalyzed organometallic reactions that have revolutionized organic synthesis
-
(e) Negishi, E. Transition metal-catalyzed organometallic reactions that have revolutionized organic synthesis. Bull. Chem. Soc. Jpn. 2007, 80, 233-257;
-
(2007)
Bull. Chem. Soc. Jpn
, vol.80
, pp. 233-257
-
-
Negishi, E.1
-
10
-
-
33846893890
-
Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts
-
(f) Yin, L.; Liebscher, J. Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 2007, 107, 133-173.
-
(2007)
Chem. Rev
, vol.107
, pp. 133-173
-
-
Yin, L.1
Liebscher, J.2
-
11
-
-
0037165715
-
Nickel-catalyzed cross-coupling reaction of Grignard reagents with alkyl halides and tosylates: Remarkable effect of 1,3-butadienes
-
(a) Terao, J.; Watanabe, H.; Ikumi, A.; Kuniyasu, H.; Kambe, N. Nickel-catalyzed cross-coupling reaction of Grignard reagents with alkyl halides and tosylates: Remarkable effect of 1,3-butadienes. J. Am. Chem. Soc. 2002, 124, 4222-4223;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 4222-4223
-
-
Terao, J.1
Watanabe, H.2
Ikumi, A.3
Kuniyasu, H.4
Kambe, N.5
-
12
-
-
19544373479
-
Iron-catalyzed homo-coupling of simple and functionalized arylmagnesium reagents
-
(b) Cahiez, G.; Chaboche, C.; Mahuteau-Betzer, F.; Ahr, M. Iron-catalyzed homo-coupling of simple and functionalized arylmagnesium reagents. Org. Lett. 2005, 7, 1943-1946;
-
(2005)
Org. Lett
, vol.7
, pp. 1943-1946
-
-
Cahiez, G.1
Chaboche, C.2
Mahuteau-Betzer, F.3
Ahr, M.4
-
13
-
-
33747419242
-
Iron-catalyzed homocoupling of bromide compounds
-
(c) Xu, X.; Cheng, D.; Pei, W. Iron-catalyzed homocoupling of bromide compounds. J. Org. Chem. 2006, 71, 6637-6639.
-
(2006)
J. Org. Chem
, vol.71
, pp. 6637-6639
-
-
Xu, X.1
Cheng, D.2
Pei, W.3
-
14
-
-
0000689303
-
Vinylation of Grignard reagents: Catalysis by iron
-
(a) Tamura, M.; Kochi, J. K. Vinylation of Grignard reagents: Catalysis by iron. J. Am. Chem. Soc. 1971, 93, 1487-1489;
-
(1971)
J. Am. Chem. Soc
, vol.93
, pp. 1487-1489
-
-
Tamura, M.1
Kochi, J.K.2
-
15
-
-
84989564580
-
Coupling of Grignard reagents with organic halides
-
(b) Tamura, M.; Kochi, J. K. Coupling of Grignard reagents with organic halides. Synthesis 1971, 303-305;
-
(1971)
Synthesis
, pp. 303-305
-
-
Tamura, M.1
Kochi, J.K.2
-
16
-
-
0001573925
-
Copper-catalyzed coupling of Grignard reagents and alkyl halides in tetrahydrofuran solutions
-
(c) Tamura, M.; Kochi, J. K. Copper-catalyzed coupling of Grignard reagents and alkyl halides in tetrahydrofuran solutions. J. Organomet. Chem. 1972, 42, 205-228;
-
(1972)
J. Organomet. Chem
, vol.42
, pp. 205-228
-
-
Tamura, M.1
Kochi, J.K.2
-
17
-
-
0000247876
-
Electron-transfer mechanisms for organometallic intermediates in catalytic reactions
-
(d) Kochi, J. K. Electron-transfer mechanisms for organometallic intermediates in catalytic reactions. Acc. Chem. Res. 1974, 7, 351-360;
-
(1974)
Acc. Chem. Res
, vol.7
, pp. 351-360
-
-
Kochi, J.K.1
-
18
-
-
33847802043
-
Synthesis of olefins: Cross coupling of alkenyl halides and Grignard reagents catalyzed by iron complexes
-
(e) Neumann, S. M.; Kochi, J. K. Synthesis of olefins: Cross coupling of alkenyl halides and Grignard reagents catalyzed by iron complexes. J. Org. Chem. 1975, 40, 599-606;
-
(1975)
J. Org. Chem
, vol.40
, pp. 599-606
-
-
Neumann, S.M.1
Kochi, J.K.2
-
19
-
-
0001109080
-
Mechanistic studies of iron catalysis in the cross coupling of alkenyl halides and Grignard reagents
-
(f) Smith, R. S.; Kochi, J. K. Mechanistic studies of iron catalysis in the cross coupling of alkenyl halides and Grignard reagents. J. Org. Chem. 1976, 41, 502-509;
-
(1976)
J. Org. Chem
, vol.41
, pp. 502-509
-
-
Smith, R.S.1
Kochi, J.K.2
-
20
-
-
0036643488
-
Homocoupling, disproportionation and cross coupling of alkyl groups: Role of the transition metal catalyst
-
For a review, see
-
(g) For a review, see Kochi, J. K. Homocoupling, disproportionation and cross coupling of alkyl groups: Role of the transition metal catalyst. J. Organomet. Chem. 2002, 653, 11-19.
-
(2002)
J. Organomet. Chem
, vol.653
, pp. 11-19
-
-
Kochi, J.K.1
-
21
-
-
0030964143
-
-
Literature references in this field of applications are far too numerous to be covered herein. Therefore, only a very limited selection of leading contributions is given: (a) Burns, D. H.; Miller, J. D.; Chan, H.-K.; Delaney, M. O. Scope and utility of a new soluble copper catalyst [CuBr-LiSPh-LiBr-THF]: A comparison with other copper catalysts in their ability to couple one equivalent of a Grignard reagent with an alkyl sulfonate. J. Am. Chem. Soc. 1997, 119, 2125-2133, and references cited therein;
-
Literature references in this field of applications are far too numerous to be covered herein. Therefore, only a very limited selection of leading contributions is given: (a) Burns, D. H.; Miller, J. D.; Chan, H.-K.; Delaney, M. O. Scope and utility of a new soluble copper catalyst [CuBr-LiSPh-LiBr-THF]: A comparison with other copper catalysts in their ability to couple one equivalent of a Grignard reagent with an alkyl sulfonate. J. Am. Chem. Soc. 1997, 119, 2125-2133, and references cited therein;
-
-
-
-
22
-
-
0034725031
-
Cu-catalyzed alkylation of Grignard reagents: A new efficient procedure
-
(b) Cahiez, G.; Chaboche, C.; Jézéquel, M. Cu-catalyzed alkylation of Grignard reagents: A new efficient procedure. Tetrahedron 2000, 56, 2733-2737;
-
(2000)
Tetrahedron
, vol.56
, pp. 2733-2737
-
-
Cahiez, G.1
Chaboche, C.2
Jézéquel, M.3
-
23
-
-
0037146041
-
Iron-catalyzed cross-coupling reactions
-
(c) Fürstner, A.; Leitner, A.; Méndez, M.; Krause, H. Iron-catalyzed cross-coupling reactions. J. Am. Chem. Soc. 2002, 124, 13856-13863;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 13856-13863
-
-
Fürstner, A.1
Leitner, A.2
Méndez, M.3
Krause, H.4
-
24
-
-
2442655977
-
Iron-catalyzed Grignard cross-coupling with alkyl halides possessing β-hydrogens
-
(d) Nagano, T.; Hayashi, T. Iron-catalyzed Grignard cross-coupling with alkyl halides possessing β-hydrogens. Org. Lett. 2004, 6, 1297-1299;
-
(2004)
Org. Lett
, vol.6
, pp. 1297-1299
-
-
Nagano, T.1
Hayashi, T.2
-
25
-
-
1642361256
-
Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl Grignard reagents
-
(e) Nakamura, M.; Matsuo, K.; Ito, S.; Nakamura, E. Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl Grignard reagents. J. Am. Chem. Soc. 2004, 126, 3686-3687;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 3686-3687
-
-
Nakamura, M.1
Matsuo, K.2
Ito, S.3
Nakamura, E.4
-
26
-
-
33644770072
-
An iron-containing ionic liquid as recyclable catalyst for aryl Grignard cross-coupling of alkyl halides
-
(f) Bica, K.; Gaertner, P. An iron-containing ionic liquid as recyclable catalyst for aryl Grignard cross-coupling of alkyl halides. Org. Lett. 2006, 8, 733-735;
-
(2006)
Org. Lett
, vol.8
, pp. 733-735
-
-
Bica, K.1
Gaertner, P.2
-
27
-
-
33645025382
-
Iron nanoparticles in the coupling of alkyl halides with aryl Grignard reagents
-
(g) Bedford, R. B.; Betham, M.; Bruce, D. W.; Davis, S. A.; Frost, R. M.; Hird, M. Iron nanoparticles in the coupling of alkyl halides with aryl Grignard reagents. Chem. Commun. 2006, 1398-1400;
-
(2006)
Chem. Commun
, pp. 1398-1400
-
-
Bedford, R.B.1
Betham, M.2
Bruce, D.W.3
Davis, S.A.4
Frost, R.M.5
Hird, M.6
-
28
-
-
34250863375
-
Copper-catalyzed cross-coupling reactions of Grignard reagents with primary-alkyl halides: Remarkable effect of 1-phenylpropyne
-
(h) Terao, J.; Todo, H.; Begum, S. A.; Kuniyasu, H.; Kambe, N. Copper-catalyzed cross-coupling reactions of Grignard reagents with primary-alkyl halides: Remarkable effect of 1-phenylpropyne. Angew. Chem. Int. Ed. 2007, 46, 2086-2089.
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 2086-2089
-
-
Terao, J.1
Todo, H.2
Begum, S.A.3
Kuniyasu, H.4
Kambe, N.5
-
29
-
-
13844254448
-
Iron-catalyzed oxidative homo-coupling or aryl Grignard reagents
-
(a) Nagano, T.; Hayashi, T. Iron-catalyzed oxidative homo-coupling or aryl Grignard reagents. Org. Lett. 2005, 7, 491-493;
-
(2005)
Org. Lett
, vol.7
, pp. 491-493
-
-
Nagano, T.1
Hayashi, T.2
-
30
-
-
15744385464
-
Ni-catalyzed alkylative dimerization of vinyl Grignard reagents using alkyl fluorides
-
(b) Terao, J.; Watabe, H.; Kambe, N. Ni-catalyzed alkylative dimerization of vinyl Grignard reagents using alkyl fluorides. J. Am. Chem. Soc. 2005, 127, 3656-3657;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 3656-3657
-
-
Terao, J.1
Watabe, H.2
Kambe, N.3
-
31
-
-
33746710039
-
Transition-metal-free homocoupling of organomagnesium compounds
-
(c) Krasovskiy, A.; Tishkov, A.; Del Amo, V.; Mayr, H.; Knochel, P. Transition-metal-free homocoupling of organomagnesium compounds. Angew. Chem. Int. Ed. 2006, 45, 5010-5014;
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 5010-5014
-
-
Krasovskiy, A.1
Tishkov, A.2
Del Amo, V.3
Mayr, H.4
Knochel, P.5
-
32
-
-
33646037027
-
Functionalized magnesium organometallics as versatile intermediates for the synthesis of polyfunctional heterocycles
-
(d) Ila, H.; Baron, O.; Wagner, A. J.; Knochel, P. Functionalized magnesium organometallics as versatile intermediates for the synthesis of polyfunctional heterocycles. Chem. Commun. 2006, 583-593;
-
(2006)
Chem. Commun
, pp. 583-593
-
-
Ila, H.1
Baron, O.2
Wagner, A.J.3
Knochel, P.4
-
33
-
-
33645120854
-
Preparation and reactions of heteroaryl organomagnesium compounds
-
(e) Ila, H.; Baron, O.; Wagner, A. J.; Knochel, P. Preparation and reactions of heteroaryl organomagnesium compounds. Chem. Lett. 2006, 35, 2-7;
-
(2006)
Chem. Lett
, vol.35
, pp. 2-7
-
-
Ila, H.1
Baron, O.2
Wagner, A.J.3
Knochel, P.4
-
34
-
-
36148956710
-
Manganese- or iron-catalyzed homocoupling of Grignard reagents using atmospheric oxygen as an oxidant
-
(f) Cahiez, G.; Moyeux, A.; Buendia, J.; Duplais, C. Manganese- or iron-catalyzed homocoupling of Grignard reagents using atmospheric oxygen as an oxidant. J. Am. Chem. Soc. 2007, 129, 13788-13789;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 13788-13789
-
-
Cahiez, G.1
Moyeux, A.2
Buendia, J.3
Duplais, C.4
-
35
-
-
51349093080
-
Efficient homocoupling reactions of halide compounds catalyzed by manganese (II) chloride
-
(g) Yuan, Y.; Bian, Y. Efficient homocoupling reactions of halide compounds catalyzed by manganese (II) chloride. Appl. Organomet. Chem. 2007, 22, 15-18;
-
(2007)
Appl. Organomet. Chem
, vol.22
, pp. 15-18
-
-
Yuan, Y.1
Bian, Y.2
-
37
-
-
0038551881
-
Hydrocarbon products from the reactions of methyllithium and ethylmagnesium bromide with heavy metal salts
-
(a) Gilman, H.; Jones, R. G.; Woods, L. A. Hydrocarbon products from the reactions of methyllithium and ethylmagnesium bromide with heavy metal salts. J. Am. Chem. Soc. 1954, 76, 3615-3617;
-
(1954)
J. Am. Chem. Soc
, vol.76
, pp. 3615-3617
-
-
Gilman, H.1
Jones, R.G.2
Woods, L.A.3
-
38
-
-
15844396245
-
Synthese von diene aus vinylhalogeniden über organokupferverbindungen.
-
(b) Kaufmann, T.; Sahm, W. Synthese von diene aus vinylhalogeniden über organokupferverbindungen. Angew. Chem. 1967, 79, 101;
-
(1967)
Angew. Chem
, vol.79
, pp. 101
-
-
Kaufmann, T.1
Sahm, W.2
-
39
-
-
34248581662
-
(II) triflate-induced oxidative coupling of Grignard reagents
-
(c) Lee, J. I. Copper(II) triflate-induced oxidative coupling of Grignard reagents. J. Korean Chem. Soc. 2005, 49, 117-120.
-
(2005)
J. Korean Chem. Soc
, vol.49
, pp. 117-120
-
-
Lee, J.I.C.1
-
40
-
-
20144379689
-
Conjugated oligoenynes based on the diethynylethene unit
-
For a review, see
-
For a review, see Nielsen, M. B.; Diedrich, F. Conjugated oligoenynes based on the diethynylethene unit. Chem. Rev. 2005, 105, 1837-1867.
-
(2005)
Chem. Rev
, vol.105
, pp. 1837-1867
-
-
Nielsen, M.B.1
Diedrich, F.2
-
41
-
-
0037233585
-
-
2O-Li-DTBB (cat.). Synthesis 2003, 443-447;
-
2O-Li-DTBB (cat.). Synthesis 2003, 443-447;
-
-
-
-
42
-
-
3242715766
-
-
2O-Li-DTBB (cat.) combination. Appl. Catal. A: Gen. 2004, 271, 171-176;
-
2O-Li-DTBB (cat.) combination. Appl. Catal. A: Gen. 2004, 271, 171-176;
-
-
-
-
43
-
-
15044353949
-
-
2O-Li-DTBB (cat.) system. Tetrahedron 2005, 61, 3859-3864.
-
2O-Li-DTBB (cat.) system. Tetrahedron 2005, 61, 3859-3864.
-
-
-
-
44
-
-
32844474451
-
-
2O-Li-arene (cat.) system, see (a) Moglie, Y.; Alonso, F.; Vitale, C.; Yus, M.; Radivoy, G. New active iron-based reducing system for carbonyl compounds and imines: Stereoselective reduction of cyclic ketones. Tetrahedron 2006, 62, 2812-2819;
-
2O-Li-arene (cat.) system, see (a) Moglie, Y.; Alonso, F.; Vitale, C.; Yus, M.; Radivoy, G. New active iron-based reducing system for carbonyl compounds and imines: Stereoselective reduction of cyclic ketones. Tetrahedron 2006, 62, 2812-2819;
-
-
-
-
45
-
-
33748104235
-
Active-iron-promoted hydrodehalogenation of organic halides
-
(b) Moglie, Y.; Alonso, F.; Vitale, C.; Yus, M.; Radivoy, G. Active-iron-promoted hydrodehalogenation of organic halides. Appl. Catal. A: Gen. 2006, 313, 94-100.
-
(2006)
Appl. Catal. A: Gen
, vol.313
, pp. 94-100
-
-
Moglie, Y.1
Alonso, F.2
Vitale, C.3
Yus, M.4
Radivoy, G.5
-
46
-
-
39149145131
-
Synthesis of azo compounds by nanosized iron-promoted reductive coupling of aromatic nitro compounds
-
Moglie, Y.; Vitale, C.; Radivoy, G. Synthesis of azo compounds by nanosized iron-promoted reductive coupling of aromatic nitro compounds. Tetrahedron Lett. 2008, 49, 1828-1831.
-
(2008)
Tetrahedron Lett
, vol.49
, pp. 1828-1831
-
-
Moglie, Y.1
Vitale, C.2
Radivoy, G.3
-
48
-
-
54349120980
-
-
Nesmeyanov, A. N, Kocheshkov, K. A, Eds, North Holland: Amsterdam
-
Nesmeyanov, A. N.; Kocheshkov, K. A., (Eds.) Methods of Elemento-organic Chemistry; North Holland: Amsterdam, 1967; vol. 2.
-
(1967)
Methods of Elemento-organic Chemistry
, vol.2
-
-
-
49
-
-
0033522827
-
Pyridylmagnesium chlorides from bromo and dibromopyridynes by brominemagnesium exchange: A convenient access to functionalized pyridines
-
Trécourt, F.; Breton, G.; Bonnet, V.; Mongin, F.; Marsais, F.; Quéguiner, G. Pyridylmagnesium chlorides from bromo and dibromopyridynes by brominemagnesium exchange: A convenient access to functionalized pyridines. Tetrahedron Lett. 1999, 40, 4339-4342.
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 4339-4342
-
-
Trécourt, F.1
Breton, G.2
Bonnet, V.3
Mongin, F.4
Marsais, F.5
Quéguiner, G.6
-
50
-
-
0036416337
-
An efficient high yielding approach for the homocoupling of aryl boronic acids
-
Koza, D. J.; Carita, E. An efficient high yielding approach for the homocoupling of aryl boronic acids. Synthesis 2002, 15, 2183-2186.
-
(2002)
Synthesis
, vol.15
, pp. 2183-2186
-
-
Koza, D.J.1
Carita, E.2
-
51
-
-
0001306851
-
Nickel- and palladium-catalyzed homocoupling of aryl triflates: Scope, limitation, and mechanistic aspects
-
Jutand, A.; Mosleh, A. Nickel- and palladium-catalyzed homocoupling of aryl triflates: Scope, limitation, and mechanistic aspects. J. Org. Chem. 1997, 62, 261-274.
-
(1997)
J. Org. Chem
, vol.62
, pp. 261-274
-
-
Jutand, A.1
Mosleh, A.2
-
52
-
-
0842305971
-
Synthesis of 2,2′-bipyridine: Versatile building blocks to sexy architectures and functional nanomaterials
-
Newkome, G. R.; Patri, A. K.; Holder, E.; Schubert, U. S. Synthesis of 2,2′-bipyridine: Versatile building blocks to sexy architectures and functional nanomaterials. Eur. J. Org. Chem. 2004, 235-254.
-
(2004)
Eur. J. Org. Chem
, pp. 235-254
-
-
Newkome, G.R.1
Patri, A.K.2
Holder, E.3
Schubert, U.S.4
-
53
-
-
20444443968
-
Aryl-aryl coupling via directed lithiation and oxidation
-
Surry, D. S.; Fox, D. J.; Mac Donald, S. J. F.; Spring, D. R. Aryl-aryl coupling via directed lithiation and oxidation. Chem. Commun. 2005, 2589-2590.
-
(2005)
Chem. Commun
, pp. 2589-2590
-
-
Surry, D.S.1
Fox, D.J.2
Mac Donald, S.J.F.3
Spring, D.R.4
-
54
-
-
54349099154
-
-
Grovenstein, E., Jr.; Bhatti, A. M.; Quest, D. E.; Sengupta, D.; VanDerveer, D. Carbanions, 23: Cleavages of 1,2-diphenylethane and derivatives by Cs-K-Na alloy: Competitive rates of bond scissions. J. Am. Chem. Soc. 1985, 50, 4960-4963.
-
Grovenstein, E., Jr.; Bhatti, A. M.; Quest, D. E.; Sengupta, D.; VanDerveer, D. Carbanions, 23: Cleavages of 1,2-diphenylethane and derivatives by Cs-K-Na alloy: Competitive rates of bond scissions. J. Am. Chem. Soc. 1985, 50, 4960-4963.
-
-
-
|