-
2
-
-
34347257749
-
-
Krische, M. J., Ed.; Springer: Berlin
-
Montgomery, J. and Sormunen, G. J. In Metal Catalyzed Reductive C-C Bond Formation: A Departure from Preformed Organometallic Reagents; Krische, M. J., Ed.; Springer: Berlin, 2007; Vol. 279, pp 1 - 23.
-
(2007)
Metal Catalyzed Reductive C-C Bond Formation: A Departure from Preformed Organometallic Reagents
, vol.279
, pp. 1-23
-
-
Montgomery, J.1
Sormunen, G.J.2
-
3
-
-
35948968063
-
-
Moslin, R. M., Miller-Moslin, K., and Jamison, T. F. Chem. Commun. 2007, 4441
-
(2007)
Chem. Commun.
, pp. 4441
-
-
Moslin, R.M.1
Miller-Moslin, K.2
Jamison, T.F.3
-
4
-
-
38049062493
-
-
Skucas, E., Ngai, M.-Y., Komanduri, V., and Krische, M. J. Acc. Chem. Res. 2007, 40, 1394
-
(2007)
Acc. Chem. Res.
, vol.40
, pp. 1394
-
-
Skucas, E.1
Ngai, M.-Y.2
Komanduri, V.3
Krische, M.J.4
-
5
-
-
58249100133
-
-
Bower, J. F., Kim, I. S., Patman, R. L., and Krische, M. J. Angew. Chem., Int. Ed. 2009, 48, 34
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 34
-
-
Bower, J.F.1
Kim, I.S.2
Patman, R.L.3
Krische, M.J.4
-
9
-
-
67650509632
-
-
Kerrigan, M. H., Jeon, S.-J., Chen, Y. K., Salvi, L., Carroll, P. J., and Walsh, P. J. J. Am. Chem. Soc. 2009, 131, 8434
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 8434
-
-
Kerrigan, M.H.1
Jeon, S.-J.2
Chen, Y.K.3
Salvi, L.4
Carroll, P.J.5
Walsh, P.J.6
-
10
-
-
74549172880
-
-
For an overview of regiocontrol strategies
-
For an overview of regiocontrol strategies: Reichard, H. A., McLaughlin, M., Chen, M. Z., and Micalizio, G. C. Eur. J. Org. Chem. 2010, 391
-
(2010)
Eur. J. Org. Chem.
, pp. 391
-
-
Reichard, H.A.1
McLaughlin, M.2
Chen, M.Z.3
Micalizio, G.C.4
-
11
-
-
77953076230
-
-
Many examples with aromatic, terminal, and silyl alkynes are described in ref 1. For ynamides
-
Many examples with aromatic, terminal, and silyl alkynes are described in ref 1. For ynamides
-
-
-
-
12
-
-
55949122495
-
-
Saito, N., Katayama, T., and Sato, Y. Org. Lett. 2008, 10, 3829
-
(2008)
Org. Lett.
, vol.10
, pp. 3829
-
-
Saito, N.1
Katayama, T.2
Sato, Y.3
-
13
-
-
0141534442
-
-
For diynes:
-
For diynes: Huddleston, R. R., Jang, H. Y., and Krische, M. J. J. Am. Chem. Soc. 2003, 125, 11488
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 11488
-
-
Huddleston, R.R.1
Jang, H.Y.2
Krische, M.J.3
-
14
-
-
1642354777
-
-
For enynes:
-
For enynes: Mahandru, G. M., Liu, G., and Montgomery, J. J. Am. Chem. Soc. 2004, 126, 3698
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3698
-
-
Mahandru, G.M.1
Liu, G.2
Montgomery, J.3
-
15
-
-
1842607439
-
-
Miller, K. M., Luanphaisarnnont, T., Molinaro, C., and Jamison, T. F. J. Am. Chem. Soc. 2004, 126, 4130
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4130
-
-
Miller, K.M.1
Luanphaisarnnont, T.2
Molinaro, C.3
Jamison, T.F.4
-
16
-
-
1842788947
-
-
Jang, H. Y., Huddleston, R. R., and Krische, M. J. J. Am. Chem. Soc. 2004, 126, 4664
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 4664
-
-
Jang, H.Y.1
Huddleston, R.R.2
Krische, M.J.3
-
17
-
-
9644260362
-
-
For ligand-switchable directing effects
-
For ligand-switchable directing effects: Miller, K. M. and Jamison, T. F. J. Am. Chem. Soc. 2004, 126, 15342
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15342
-
-
Miller, K.M.1
Jamison, T.F.2
-
18
-
-
15744384881
-
-
Bahadoor, A. B., Flyer, A., and Micalizio, G. C. J. Am. Chem. Soc. 2005, 127, 3694
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 3694
-
-
Bahadoor, A.B.1
Flyer, A.2
Micalizio, G.C.3
-
20
-
-
72849137918
-
-
Malik, H. A., Chaulagain, M. R., and Montgomery, J. Org. Lett. 2009, 11, 5734
-
(2009)
Org. Lett.
, vol.11
, pp. 5734
-
-
Malik, H.A.1
Chaulagain, M.R.2
Montgomery, J.3
-
21
-
-
25444480800
-
-
Knapp-Reed, B., Mahandru, G. M., and Montgomery, J. J. Am. Chem. Soc. 2005, 127, 13156
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 13156
-
-
Knapp-Reed, B.1
Mahandru, G.M.2
Montgomery, J.3
-
22
-
-
34547746450
-
-
Chaulagain, M. R., Sormunen, G. J., and Montgomery, J. J. Am. Chem. Soc. 2007, 129, 9568
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 9568
-
-
Chaulagain, M.R.1
Sormunen, G.J.2
Montgomery, J.3
-
24
-
-
77249109340
-
-
Liu, P., McCarren, P., Cheong, P. H. Y., Jamison, T. F., and Houk, K. N. J. Am. Chem. Soc. 2010, 132, 2050
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 2050
-
-
Liu, P.1
McCarren, P.2
Cheong, P.H.Y.3
Jamison, T.F.4
Houk, K.N.5
-
25
-
-
0000524458
-
-
Huang, W. S., Chan, J., and Jamison, T. F. Org. Lett. 2000, 2, 4221
-
(2000)
Org. Lett.
, vol.2
, pp. 4221
-
-
Huang, W.S.1
Chan, J.2
Jamison, T.F.3
-
26
-
-
34447529183
-
-
For regioselectivity in imine-alkyne couplings
-
For regioselectivity in imine-alkyne couplings: Barchuk, A., Ngai, M. Y., and Krische, M. J. J. Am. Chem. Soc. 2007, 129, 8432
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 8432
-
-
Barchuk, A.1
Ngai, M.Y.2
Krische, M.J.3
-
27
-
-
33646439534
-
-
Lavallo, V., Canac, Y., Donnadieu, B., Schoeller, W. W., and Bertrand, G. Science 2006, 312, 722
-
(2006)
Science
, vol.312
, pp. 722
-
-
Lavallo, V.1
Canac, Y.2
Donnadieu, B.3
Schoeller, W.W.4
Bertrand, G.5
-
28
-
-
39149086702
-
-
Kuchenbeiser, G., Donnadieu, B., and Bertrand, G. J. Organomet. Chem. 2008, 693, 899
-
(2008)
J. Organomet. Chem.
, vol.693
, pp. 899
-
-
Kuchenbeiser, G.1
Donnadieu, B.2
Bertrand, G.3
-
29
-
-
53849133109
-
-
Schoeller, W. W., Frey, G. D., and Bertrand, G. Chem. - Eur. J. 2008, 14, 4711
-
(2008)
Chem. - Eur. J.
, vol.14
, pp. 4711
-
-
Schoeller, W.W.1
Frey, G.D.2
Bertrand, G.3
-
30
-
-
77953074076
-
-
Ligand 5c is available as the racemate by the procedure employed
-
Ligand 5c is available as the racemate by the procedure employed.
-
-
-
-
31
-
-
33244482255
-
-
For development of the general structural motif
-
For development of the general structural motif: Funk, T. W., Berlin, J. M., and Grubbs, R. H. J. Am. Chem. Soc. 2006, 128, 1840
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 1840
-
-
Funk, T.W.1
Berlin, J.M.2
Grubbs, R.H.3
-
32
-
-
20444436397
-
-
For the synthesis of a precursor of 5c
-
For the synthesis of a precursor of 5c: Mercer, G. J., Sturdy, M., Jensen, D. R., and Sigman, M. S. Tetrahedron 2005, 61, 6418
-
(2005)
Tetrahedron
, vol.61
, pp. 6418
-
-
Mercer, G.J.1
Sturdy, M.2
Jensen, D.R.3
Sigman, M.S.4
-
33
-
-
33750183982
-
-
For the role of base structure in deprotonation of 6
-
For the role of base structure in deprotonation of 6: Lavallo, V., Ishida, Y., Donnadieu, B., and Bertrand, G. Angew. Chem., Int. Ed. 2006, 45, 6652
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6652
-
-
Lavallo, V.1
Ishida, Y.2
Donnadieu, B.3
Bertrand, G.4
-
34
-
-
33745350526
-
-
For alternate access to the 1,1-disubstituted isomer
-
For alternate access to the 1,1-disubstituted isomer: Takai, K., Sakamoto, S., Isshiki, T., and Kokumai, T. Tetrahedron 2006, 62, 7534
-
(2006)
Tetrahedron
, vol.62
, pp. 7534
-
-
Takai, K.1
Sakamoto, S.2
Isshiki, T.3
Kokumai, T.4
-
35
-
-
77953079031
-
-
For discussions of ligand size effects
-
For discussions of ligand size effects
-
-
-
-
36
-
-
3342989847
-
-
Tekavec, T. N., Arif, A. M., and Louie, J. Tetrahedron 2004, 60, 7431
-
(2004)
Tetrahedron
, vol.60
, pp. 7431
-
-
Tekavec, T.N.1
Arif, A.M.2
Louie, J.3
-
37
-
-
14744269446
-
-
Dorta, R., Stevens, E. D., Scott, N. M., Costabile, C., Cavallo, L., Hoff, C. D., and Nolan, S. P. J. Am. Chem. Soc. 2005, 127, 2485
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2485
-
-
Dorta, R.1
Stevens, E.D.2
Scott, N.M.3
Costabile, C.4
Cavallo, L.5
Hoff, C.D.6
Nolan, S.P.7
-
38
-
-
77950202768
-
-
Ragone, F., Poater, A., and Cavallo, L. J. Am. Chem. Soc. 2010, 132, 4249
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 4249
-
-
Ragone, F.1
Poater, A.2
Cavallo, L.3
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