-
1
-
-
0003441482
-
-
Wiley, Chichester
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(2004)
Palladium Reagents and Catalysts
-
-
Tsuji, J.1
-
2
-
-
0003397781
-
-
Wiley-VCH, Weinheim
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(2004)
Metal-catalyzed Cross-coupling Reactions
-
-
Diederich, F.1
De Meijere, A.2
-
3
-
-
0003779363
-
-
(Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(2004)
Transition Metals for Organic Synthesis, Vol. 1, 2nd Ed.
, vol.1
, pp. 208
-
-
Stara, G.1
Riermeier, T.H.2
Beller, M.3
-
4
-
-
0000258045
-
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(1999)
Top. Organomet. Chem.
, vol.3
, pp. 193
-
-
Grushin, V.V.1
Alper, H.2
-
5
-
-
0003995267
-
-
Wiley-Interscience, New York
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
-
-
Negishi, E.1
-
6
-
-
4344692348
-
Cross-coupling reactions: A practical guide
-
For some recent reviews see: a) J. Tsuji Palladium Reagents and Catalysts, Wiley, Chichester, 2004; b) Metal-Catalyzed Cross-Coupling Reactions (Eds.: F. Diederich, A. de Meijere), Wiley-VCH, Weinheim, 2004; c) G. Stara, T. H. Riermeier, M. Beller in Transition Metals for Organic Synthesis, Vol. 1, 2nd ed. (Eds.: M. Beller, C. Bolm), Wiley-VCH, Weinheim, 2004, pp.208; d) V. V. Grushin, H. Alper, Top. Organomet. Chem. 1999, 3, 193. e) Handbook of Organopalladium Chemistry for Organic Synthesis (Ed.: E. Negishi), Wiley-Interscience, New York, 2002; f) "Cross-Coupling Reactions: A Practical Guide" in Topics in Current Chemistry, Vol. 219 (Ed.: N. Miyaura), 2002.
-
(2002)
Topics in Current Chemistry
, vol.219
-
-
Miyaura, N.1
-
7
-
-
0037184777
-
-
For some recent examples of multifunctional Pd catalysts that promote sequential one-pot processes see: a) G. Poli, G. Giambastiani, J. Org. Chem. 2002, 67, 9456-9459; b) A. N. Thadani, V. H. Rawal, Org. Lett. 2002, 4, 4321-4323; c) F. Faccini, E. Motti, M. Catellani, J. Am. Chem. Soc. 2004, 126, 78-79, and references therein.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 9456-9459
-
-
Poli, G.1
Giambastiani, G.2
-
8
-
-
0037191628
-
-
For some recent examples of multifunctional Pd catalysts that promote sequential one-pot processes see: a) G. Poli, G. Giambastiani, J. Org. Chem. 2002, 67, 9456-9459; b) A. N. Thadani, V. H. Rawal, Org. Lett. 2002, 4, 4321-4323; c) F. Faccini, E. Motti, M. Catellani, J. Am. Chem. Soc. 2004, 126, 78-79, and references therein.
-
(2002)
Org. Lett.
, vol.4
, pp. 4321-4323
-
-
Thadani, A.N.1
Rawal, V.H.2
-
9
-
-
0347720656
-
-
and references therein
-
For some recent examples of multifunctional Pd catalysts that promote sequential one-pot processes see: a) G. Poli, G. Giambastiani, J. Org. Chem. 2002, 67, 9456-9459; b) A. N. Thadani, V. H. Rawal, Org. Lett. 2002, 4, 4321-4323; c) F. Faccini, E. Motti, M. Catellani, J. Am. Chem. Soc. 2004, 126, 78-79, and references therein.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 78-79
-
-
Faccini, F.1
Motti, E.2
Catellani, M.3
-
10
-
-
0036408239
-
-
a) J. Barluenga, F. Aznar, M. A. Fernández, C. Valdés, Chem. Commun. 2002, 2362-2363;
-
(2002)
Chem. Commun.
, pp. 2362-2363
-
-
Barluenga, J.1
Aznar, F.2
Fernández, M.A.3
Valdés, C.4
-
11
-
-
0842305925
-
-
b) J. Barluenga, M. A. Fernández, F. Aznar, C. Valdés. Chem. Eur. J. 2004, 10. 494-507;
-
(2004)
Chem. Eur. J.
, vol.10
, pp. 494-507
-
-
Barluenga, J.1
Fernández, M.A.2
Aznar, F.3
Valdés, C.4
-
12
-
-
0002261207
-
-
c) A. Y. Lebcdev, V. V. Izmer, D. N. Kazyul'kin, I. Beletskaya. A. Z, Voskoboynikov, Org. Lett. 2002, 4, 623-626.
-
(2002)
Org. Lett.
, vol.4
, pp. 623-626
-
-
Lebcdev, A.Y.1
Izmer, V.V.2
Kazyul'kin, D.N.3
Beletskaya, I.4
Voskoboynikov, A.Z.5
-
13
-
-
3142754154
-
-
J. Barluenga, F. Aznar, M. A. Fernández, C. Valdés, Chem. Commun. 2004, 1400-1401.
-
(2004)
Chem. Commun.
, pp. 1400-1401
-
-
Barluenga, J.1
Aznar, F.2
Fernández, M.A.3
Valdés, C.4
-
14
-
-
0037049225
-
-
a) For the palladium-catalyzed animation of vinyl Inflates see: M. C. Willis, G. N. Brace, Tetrahedron Lett. 2002, 43, 9085-9088;
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 9085-9088
-
-
Willis, M.C.1
Brace, G.N.2
-
15
-
-
0142106421
-
-
for cooper-catalyzed amidations of vinyl bromides and iodides see: b) L. Jiang, G. E. Job, A. Klapars, S. L. Buchwald, Org. Lett. 2003, 5, 3667-3669;
-
(2003)
Org. Lett.
, vol.5
, pp. 3667-3669
-
-
Jiang, L.1
Job, G.E.2
Klapars, A.3
Buchwald, S.L.4
-
16
-
-
0742321841
-
-
c) C. Han, R. Shen, S. Su, J. A. Porco, Jr., Org. Lett. 2004, 6, 27-30;
-
(2004)
Org. Lett.
, vol.6
, pp. 27-30
-
-
Han, C.1
Shen, R.2
Su, S.3
Porco Jr., J.A.4
-
18
-
-
0001038733
-
-
For leading reviews in the palladium-catalyzed aryl animation, see: a) J. P. Wolfe, S. Wagaw, J. F. Marcoux, S. L. Buchwald, Acc. Chem. Res. 1998, 31, 805-818; b) J. F. Hartwig, Acc. Chem. Res. 1998, 31, 852-860; c) J. F. Hartwig in Modem Amination Methods (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2000; d) A. R. Muci, S. L. Buchwald, Top. Curr. Chem. 2002, 219, 133-209.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 805-818
-
-
Wolfe, J.P.1
Wagaw, S.2
Marcoux, J.F.3
Buchwald, S.L.4
-
19
-
-
0000037108
-
-
For leading reviews in the palladium-catalyzed aryl animation, see: a) J. P. Wolfe, S. Wagaw, J. F. Marcoux, S. L. Buchwald, Acc. Chem. Res. 1998, 31, 805-818; b) J. F. Hartwig, Acc. Chem. Res. 1998, 31, 852-860; c) J. F. Hartwig in Modem Amination Methods (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2000; d) A. R. Muci, S. L. Buchwald, Top. Curr. Chem. 2002, 219, 133-209.
-
(1998)
Acc. Chem. Res.
, vol.31
, pp. 852-860
-
-
Hartwig, J.F.1
-
20
-
-
17444374547
-
-
(Ed.: A. Ricci), Wiley-VCH, Weinheim
-
For leading reviews in the palladium-catalyzed aryl animation, see: a) J. P. Wolfe, S. Wagaw, J. F. Marcoux, S. L. Buchwald, Acc. Chem. Res. 1998, 31, 805-818; b) J. F. Hartwig, Acc. Chem. Res. 1998, 31, 852-860; c) J. F. Hartwig in Modem Amination Methods (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2000; d) A. R. Muci, S. L. Buchwald, Top. Curr. Chem. 2002, 219, 133-209.
-
(2000)
Modem Amination Methods
-
-
Hartwig, J.F.1
-
21
-
-
0000157513
-
-
For leading reviews in the palladium-catalyzed aryl animation, see: a) J. P. Wolfe, S. Wagaw, J. F. Marcoux, S. L. Buchwald, Acc. Chem. Res. 1998, 31, 805-818; b) J. F. Hartwig, Acc. Chem. Res. 1998, 31, 852-860; c) J. F. Hartwig in Modem Amination Methods (Ed.: A. Ricci), Wiley-VCH, Weinheim, 2000; d) A. R. Muci, S. L. Buchwald, Top. Curr. Chem. 2002, 219, 133-209.
-
(2002)
Top. Curr. Chem.
, vol.219
, pp. 133-209
-
-
Muci, A.R.1
Buchwald, S.L.2
-
24
-
-
10744221273
-
-
and references therein
-
A. Jutand, S. Negri, Organometallics 2003, 22, 4229-4237, and references therein.
-
(2003)
Organometallics
, vol.22
, pp. 4229-4237
-
-
Jutand, A.1
Negri, S.2
-
25
-
-
0034812321
-
-
For leading references on cross-coupling reactions with vinyl chlorides, see: a) C. Dai, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 2719-2724; b) G. Y. Li, J. Org. Chem. 2002, 67, 3643-3650.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 2719-2724
-
-
Dai, C.1
Fu, G.C.2
-
26
-
-
0037204954
-
-
For leading references on cross-coupling reactions with vinyl chlorides, see: a) C. Dai, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 2719-2724; b) G. Y. Li, J. Org. Chem. 2002, 67, 3643-3650.
-
(2002)
J. Org. Chem.
, vol.67
, pp. 3643-3650
-
-
Li, G.Y.1
-
27
-
-
0032560932
-
-
D. W. Old, J. P. Wolfe, S. L. Buchwald, J. Am. Chem. Soc. 1998, 120, 9722-9723.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 9722-9723
-
-
Old, D.W.1
Wolfe, J.P.2
Buchwald, S.L.3
-
28
-
-
0037112673
-
-
For a recent review in the cross-coupling reactions of aryl chlorides: A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4176-4211; Angew. Chem. Int. Ed. 2000, 41, 4176-4211;.
-
(2002)
Angew. Chem.
, vol.114
, pp. 4176-4211
-
-
Littke, A.F.1
Fu, G.C.2
-
29
-
-
0037112673
-
-
For a recent review in the cross-coupling reactions of aryl chlorides: A. F. Littke, G. C. Fu, Angew. Chem. 2002, 114, 4176-4211; Angew. Chem. Int. Ed. 2082, 41, 4176-4211;.
-
(2000)
Angew. Chem. Int. Ed.
, vol.41
, pp. 4176-4211
-
-
-
31
-
-
0034600318
-
-
3 system represents an exception to the rule as it reacts more readily with aryl chlorides than with vinyl chorides, although with low selectivity: A. F. Littke, C. Dai, G. C. Fu, J. Am. Chem. Soc. 2000, 122, 4020-4028.
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 4020-4028
-
-
Littke, A.F.1
Dai, C.2
Fu, G.C.3
-
33
-
-
0000866633
-
-
For intramolecular Heck reactions of enamines leading to indoles see: a) A. Kasahara, T. Izumi, S. Murakami, H. Yanai, M. Takatori, Bull. Chem. Soc. Jpn. 1986, 59, 927-928. A. Kasahara, T. Izumi, T. Kikuchi, X. Lin, J. Heterocycl. Chem. 1987, 24, 1555-1556; b) C. Chen, D. Lieberman, R. D. Larsen, T. R. Verhoeven, P. J. Reider, J. Org. Chem. 1997, 62, 2676-2677.
-
(1986)
Bull. Chem. Soc. Jpn.
, vol.59
, pp. 927-928
-
-
Kasahara, A.1
Izumi, T.2
Murakami, S.3
Yanai, H.4
Takatori, M.5
-
34
-
-
0343956631
-
-
For intramolecular Heck reactions of enamines leading to indoles see: a) A. Kasahara, T. Izumi, S. Murakami, H. Yanai, M. Takatori, Bull. Chem. Soc. Jpn. 1986, 59, 927-928. A. Kasahara, T. Izumi, T. Kikuchi, X. Lin, J. Heterocycl. Chem. 1987, 24, 1555-1556; b) C. Chen, D. Lieberman, R. D. Larsen, T. R. Verhoeven, P. J. Reider, J. Org. Chem. 1997, 62, 2676-2677.
-
(1987)
J. Heterocycl. Chem.
, vol.24
, pp. 1555-1556
-
-
Kasahara, A.1
Izumi, T.2
Kikuchi, T.3
Lin, X.4
-
35
-
-
0030908560
-
-
For intramolecular Heck reactions of enamines leading to indoles see: a) A. Kasahara, T. Izumi, S. Murakami, H. Yanai, M. Takatori, Bull. Chem. Soc. Jpn. 1986, 59, 927-928. A. Kasahara, T. Izumi, T. Kikuchi, X. Lin, J. Heterocycl. Chem. 1987, 24, 1555-1556; b) C. Chen, D. Lieberman, R. D. Larsen, T. R. Verhoeven, P. J. Reider, J. Org. Chem. 1997, 62, 2676-2677.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 2676-2677
-
-
Chen, C.1
Lieberman, D.2
Larsen, R.D.3
Verhoeven, T.R.4
Reider, P.J.5
-
36
-
-
17144401598
-
-
While preparing this manuscript a paper describing the intramolecular Heck reaction of enamines, generated in situ from ketones and o-chloroanilines, oriented toward the synthesis of indoles was published: M. Nazaré, C. Schneider, A. Lindenschmidt, D. W. Will, Angew. Chcm. 2004, 116, 4626-4629; Angew. Chem. Int. Ed. 2004. 43, 4526-4528.
-
(2004)
Angew. Chcm.
, vol.116
, pp. 4626-4629
-
-
Nazaré, M.1
Schneider, C.2
Lindenschmidt, A.3
Will, D.W.4
-
37
-
-
4544224760
-
-
While preparing this manuscript a paper describing the intramolecular Heck reaction of enamines, generated in situ from ketones and o-chloroanilines, oriented toward the synthesis of indoles was published: M. Nazaré, C. Schneider, A. Lindenschmidt, D. W. Will, Angew. Chcm. 2004, 116, 4626-4629; Angew. Chem. Int. Ed. 2004. 43, 4526-4528.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 4526-4528
-
-
-
38
-
-
0030017045
-
-
A. Kojima, T. Takemoto, M. Sodeoka, M. Shibasaki, J. Org. Chem. 1996, 61, 4876-4877.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 4876-4877
-
-
Kojima, A.1
Takemoto, T.2
Sodeoka, M.3
Shibasaki, M.4
-
39
-
-
0035903689
-
-
a) P. von Zezschwitz, F. Petry, A. de Meijere, Chem. Eur. J. 2001, 7. 4035-4046; b) H. W. Sünnemann, A. de Meijere, Angew. Chem. 2004, 116, 913-915; Angew. Chem. Int. Ed. 2004, 43, 895-897;.
-
(2001)
Chem. Eur. J.
, vol.7
, pp. 4035-4046
-
-
Von Zezschwitz, P.1
Petry, F.2
De Meijere, A.3
-
40
-
-
4644367503
-
-
a) P. von Zezschwitz, F. Petry, A. de Meijere, Chem. Eur. J. 2001, 7. 4035-4046; b) H. W. Sünnemann, A. de Meijere, Angew. Chem. 2004, 116, 913-915; Angew. Chem. Int. Ed. 2004, 43, 895-897;.
-
(2004)
Angew. Chem.
, vol.116
, pp. 913-915
-
-
Sünnemann, H.W.1
De Meijere, A.2
-
41
-
-
4544333057
-
-
a) P. von Zezschwitz, F. Petry, A. de Meijere, Chem. Eur. J. 2001, 7. 4035-4046; b) H. W. Sünnemann, A. de Meijere, Angew. Chem. 2004, 116, 913-915; Angew. Chem. Int. Ed. 2004, 43, 895-897;.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 895-897
-
-
-
42
-
-
0036406094
-
-
For one-pot sequential processes involving Pd-catalyzed aryl aminations see: a) R. B. Bedford, C. S. J. Cazin, Chem. Commun. 2002, 2310-2311; b) G. Cuny, M. Boys-Chousy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925; Angew. Chem. Int. Ed. 2003, 42, 4774-4777; c) R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762; d) R. Lira, J. P. Wolfe, J. Am. Chem. Soc. 2004, 126, 13906-13907.
-
(2002)
Chem. Commun.
, pp. 2310-2311
-
-
Bedford, R.B.1
Cazin, C.S.J.2
-
43
-
-
17444381095
-
-
For one-pot sequential processes involving Pd-catalyzed aryl aminations see: a) R. B. Bedford, C. S. J. Cazin, Chem. Commun. 2002, 2310-2311; b) G. Cuny, M. Boys-Chousy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925; Angew. Chem. Int. Ed. 2003, 42, 4774-4777; c) R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762; d) R. Lira, J. P. Wolfe, J. Am. Chem. Soc. 2004, 126, 13906-13907.
-
(2003)
Angew. Chem.
, vol.115
, pp. 4922-4925
-
-
Cuny, G.1
Boys-Chousy, M.2
Zhu, J.3
-
44
-
-
0142183595
-
-
For one-pot sequential processes involving Pd-catalyzed aryl aminations see: a) R. B. Bedford, C. S. J. Cazin, Chem. Commun. 2002, 2310-2311; b) G. Cuny, M. Boys-Chousy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925; Angew. Chem. Int. Ed. 2003, 42, 4774-4777; c) R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762; d) R. Lira, J. P. Wolfe, J. Am. Chem. Soc. 2004, 126, 13906-13907.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 4774-4777
-
-
-
45
-
-
11844306017
-
-
For one-pot sequential processes involving Pd-catalyzed aryl aminations see: a) R. B. Bedford, C. S. J. Cazin, Chem. Commun. 2002, 2310-2311; b) G. Cuny, M. Boys-Chousy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925; Angew. Chem. Int. Ed. 2003, 42, 4774-4777; c) R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762; d) R. Lira, J. P. Wolfe, J. Am. Chem. Soc. 2004, 126, 13906-13907.
-
(2004)
Org. Lett.
, vol.6
, pp. 4759-4762
-
-
Ferraccioli, R.1
Carenzi, D.2
Rombola, O.3
Catellani, M.4
-
46
-
-
7444269099
-
-
For one-pot sequential processes involving Pd-catalyzed aryl aminations see: a) R. B. Bedford, C. S. J. Cazin, Chem. Commun. 2002, 2310-2311; b) G. Cuny, M. Boys-Chousy, J. Zhu, Angew. Chem. 2003, 115, 4922-4925; Angew. Chem. Int. Ed. 2003, 42, 4774-4777; c) R. Ferraccioli, D. Carenzi, O. Rombola, M. Catellani, Org. Lett. 2004, 6, 4759-4762; d) R. Lira, J. P. Wolfe, J. Am. Chem. Soc. 2004, 126, 13906-13907.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 13906-13907
-
-
Lira, R.1
Wolfe, J.P.2
-
47
-
-
0003660996
-
-
Pergamon Press, Oxford
-
For reviews on Pd-catalyzed methods for the synthesis of indoles see: a) J. J. Li, G. W. Gribble, Palladium in Heterocyclic Chemistry, Pergamon Press, Oxford, 2001; b) T. L. Gilchrist, J. Chem. Soc. Perkin Trans, 1 2001, 2491-2515.
-
(2001)
Palladium in Heterocyclic Chemistry
-
-
Li, J.J.1
Gribble, G.W.2
-
48
-
-
0034740911
-
-
For reviews on Pd-catalyzed methods for the synthesis of indoles see: a) J. J. Li, G. W. Gribble, Palladium in Heterocyclic Chemistry, Pergamon Press, Oxford, 2001; b) T. L. Gilchrist, J. Chem. Soc. Perkin Trans, 1 2001, 2491-2515.
-
(2001)
J. Chem. Soc. Perkin Trans, 1
, pp. 2491-2515
-
-
Gilchrist, T.L.1
-
49
-
-
0000428035
-
-
A well-established method for the synthesis of indoles from o-iodo-anilines and alkynes by a Pd-catalyzed domino process is the Larock indole synthesis: a) R. C. Larock, E. K. Yum, J. Am. Chem. Soc. 1991, 113, 6689-6690; b) R. C. Larock, E. K. Yum, J. Org. Chem. 1998, 63, 7652-7662.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6689-6690
-
-
Larock, R.C.1
Yum, E.K.2
-
50
-
-
33744870975
-
-
A well-established method for the synthesis of indoles from o-iodo-anilines and alkynes by a Pd-catalyzed domino process is the Larock indole synthesis: a) R. C. Larock, E. K. Yum, J. Am. Chem. Soc. 1991, 113, 6689-6690; b) R. C. Larock, E. K. Yum, J. Org. Chem. 1998, 63, 7652-7662.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 7652-7662
-
-
Larock, R.C.1
Yum, E.K.2
-
51
-
-
1542352875
-
-
For some other relevant recent approaches to the indole ring see: a) H. Siebeneicher, I. Bytschkov, S. Doye, Angew. Chem. 2003, 115, 3151-3153; Angew. Chem. Int. Ed. 2003, 42, 3042-3044; b) J. Barluenga, M. Trincado, E. Rubio, J. González, Angew. Chem. 2003, 115, 2508-2511; Angew. Chem. Int. Ed. 2003, 42, 2406-2409;, and references therein.
-
(2003)
Angew. Chem.
, vol.115
, pp. 3151-3153
-
-
Siebeneicher, H.1
Bytschkov, I.2
Doye, S.3
-
52
-
-
0042808535
-
-
For some other relevant recent approaches to the indole ring see: a) H. Siebeneicher, I. Bytschkov, S. Doye, Angew. Chem. 2003, 115, 3151-3153; Angew. Chem. Int. Ed. 2003, 42, 3042-3044; b) J. Barluenga, M. Trincado, E. Rubio, J. González, Angew. Chem. 2003, 115, 2508-2511; Angew. Chem. Int. Ed. 2003, 42, 2406-2409;, and references therein.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 3042-3044
-
-
-
53
-
-
0141675249
-
-
For some other relevant recent approaches to the indole ring see: a) H. Siebeneicher, I. Bytschkov, S. Doye, Angew. Chem. 2003, 115, 3151-3153; Angew. Chem. Int. Ed. 2003, 42, 3042-3044; b) J. Barluenga, M. Trincado, E. Rubio, J. González, Angew. Chem. 2003, 115, 2508-2511; Angew. Chem. Int. Ed. 2003, 42, 2406-2409;, and references therein.
-
(2003)
Angew. Chem.
, vol.115
, pp. 2508-2511
-
-
Barluenga, J.1
Trincado, M.2
Rubio, E.3
González, J.4
-
54
-
-
0038343546
-
-
and references therein
-
For some other relevant recent approaches to the indole ring see: a) H. Siebeneicher, I. Bytschkov, S. Doye, Angew. Chem. 2003, 115, 3151-3153; Angew. Chem. Int. Ed. 2003, 42, 3042-3044; b) J. Barluenga, M. Trincado, E. Rubio, J. González, Angew. Chem. 2003, 115, 2508-2511; Angew. Chem. Int. Ed. 2003, 42, 2406-2409;, and references therein.
-
(2003)
Angew. Chem. Int. Ed.
, vol.42
, pp. 2406-2409
-
-
-
55
-
-
17444367948
-
-
note
-
Two equivalents of base are required to carry out the cascade process, as one equivalent is consumed in each step.
-
-
-
-
56
-
-
17444406935
-
-
note
-
DavePhos and JohnPhos are currently the commercial names for 2-dicyclohexylphosphino-2'-N,N-dimethylaminobiphenyl and 2-di-tert- butylphosphinobiphenyl, respectively.
-
-
-
-
57
-
-
0038579438
-
-
X. Huang, K. W. Anderson, D. Zim, L. Jiang, A. Klapars, S. L. Buchwald, J. Am. Chem. Soc. 2003, 125, 6653-6655.
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 6653-6655
-
-
Huang, X.1
Anderson, K.W.2
Zim, D.3
Jiang, L.4
Klapars, A.5
Buchwald, S.L.6
-
58
-
-
0000588892
-
-
S. Hara, H. Dojo, S. Takinami, A. Suzuki, Tetrahedron Lett. 1983, 24, 731-734.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 731-734
-
-
Hara, S.1
Dojo, H.2
Takinami, S.3
Suzuki, A.4
-
60
-
-
0000154154
-
-
J. Schwartz, J. A. Labinger, Angew. Chem. 1976, 88, 402-409; Angew. Chem. Int. Ed. Engl 1976, 15, 333-336.
-
(1976)
Angew. Chem.
, vol.88
, pp. 402-409
-
-
Schwartz, J.1
Labinger, J.A.2
-
61
-
-
84982433710
-
-
J. Schwartz, J. A. Labinger, Angew. Chem. 1976, 88, 402-409; Angew. Chem. Int. Ed. Engl 1976, 15, 333-336.
-
(1976)
Angew. Chem. Int. Ed. Engl
, vol.15
, pp. 333-336
-
-
-
62
-
-
0141789718
-
-
Z-X. Jiang, Y-Y. Qin, F-L. Ping, J. Org. Chem. 2003, 68, 7544-7547.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 7544-7547
-
-
Jiang, Z.-X.1
Qin, Y.-Y.2
Ping, F.-L.3
-
64
-
-
0019815529
-
-
W. J. Houlihan, I. Uike, V. A. Parrino, J. Org. Chem. 1981, 46, 4511-4515.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 4511-4515
-
-
Houlihan, W.J.1
Uike, I.2
Parrino, V.A.3
-
65
-
-
0342285860
-
-
G. Bartola, G. Palmieri, M. Petrini, M. Bosco, R. Dalpozzo, Tetrahedron 1990, 46, 1379-1384
-
(1990)
Tetrahedron
, vol.46
, pp. 1379-1384
-
-
Bartola, G.1
Palmieri, G.2
Petrini, M.3
Bosco, M.4
Dalpozzo, R.5
-
66
-
-
0001150685
-
-
A. B. Smith III, M. Visnick, J. N. Haseltine, P. A. Sprengeler, Tetrahedron 1986, 42, 2957-2969.
-
(1986)
Tetrahedron
, vol.42
, pp. 2957-2969
-
-
Smith III, A.B.1
Visnick, M.2
Haseltine, J.N.3
Sprengeler, P.A.4
-
68
-
-
0033763474
-
-
J. G. Rodríguez, A. Lafuente, P. Garera-Almaraz, J. Heterocycl. Chem. 2000, 37, 1281-1288.
-
(2000)
J. Heterocycl. Chem.
, vol.37
, pp. 1281-1288
-
-
Rodríguez, J.G.1
Lafuente, A.2
Garera-Almaraz, P.3
|