-
1
-
-
0037000811
-
-
For reviews on enantioselective carbonyl allylation, see: a
-
For reviews on enantioselective carbonyl allylation, see: a) P. V. Ramachandran, Aldrichimica Acta 2002, 35, 23-35;
-
(2002)
Aldrichimica Acta
, vol.35
, pp. 23-35
-
-
Ramachandran, P.V.1
-
3
-
-
0142245730
-
-
Angew. Chem. Int. Ed. 2003, 42, 4732-4739;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4732-4739
-
-
-
5
-
-
33646567165
-
-
d) C.-M. Yu, J. Youn, H.-K. Jung, Bull. Korean Chem. Soc. 2006, 27, 463-472;
-
(2006)
Bull. Korean Chem. Soc
, vol.27
, pp. 463-472
-
-
Yu, C.-M.1
Youn, J.2
Jung, H.-K.3
-
7
-
-
34447549207
-
-
f) D. G. Hall, Synlett 2007, 1644-1655.
-
(2007)
Synlett
, pp. 1644-1655
-
-
Hall, D.G.1
-
11
-
-
58249112714
-
-
Chirally modified allyl metal reagents: a T. Herold, R. W. Hoffmann, Angew. Chem. 1978, 90, 822-823;
-
Chirally modified allyl metal reagents: a) T. Herold, R. W. Hoffmann, Angew. Chem. 1978, 90, 822-823;
-
-
-
-
14
-
-
0001506789
-
-
c) T. Hayashi, M. Konishi, M. Kumada, J. Am. Chem. Soc. 1982, 104, 4963-4965;
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 4963-4965
-
-
Hayashi, T.1
Konishi, M.2
Kumada, M.3
-
16
-
-
0000995725
-
-
e) W. R. Roush, A. E. Walts, L. K. Hoong, J. Am. Chem. Soc. 1985, 107, 8186-8190;
-
(1985)
J. Am. Chem. Soc
, vol.107
, pp. 8186-8190
-
-
Roush, W.R.1
Walts, A.E.2
Hoong, L.K.3
-
19
-
-
33845183116
-
-
h) E. J. Corey, C.-M. Yu, S. S. Kim, J. Am. Chem. Soc. 1989, 111, 5495-5496;
-
(1989)
J. Am. Chem. Soc
, vol.111
, pp. 5495-5496
-
-
Corey, E.J.1
Yu, C.-M.2
Kim, S.S.3
-
20
-
-
84987490954
-
-
i) D. Seebach, A. K. Beck, R. Imwinkelried, S. Roggo, A. Wonnacott, Helv. Chim. Acta 1987, 70, 954-974;
-
(1987)
Helv. Chim. Acta
, vol.70
, pp. 954-974
-
-
Seebach, D.1
Beck, A.K.2
Imwinkelried, R.3
Roggo, S.4
Wonnacott, A.5
-
24
-
-
0037055104
-
-
l) J. W. A. Kinnaird, P. Y. Ng, K. Kubota, X. Wang, J. L. Leighton, J. Am. Chem. Soc. 2002, 124, 7920-7921;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 7920-7921
-
-
Kinnaird, J.W.A.1
Ng, P.Y.2
Kubota, K.3
Wang, X.4
Leighton, J.L.5
-
25
-
-
9444254046
-
-
m) B. M. Hackman, P. J. Lombardi, J. L. Leighton, Org. Lett. 2004, 6, 4375-4377;
-
(2004)
Org. Lett
, vol.6
, pp. 4375-4377
-
-
Hackman, B.M.1
Lombardi, P.J.2
Leighton, J.L.3
-
26
-
-
20444399909
-
-
n) C. H. Burgos, E. Canales, K. Matos, J. A. Soderquist, J. Am. Chem. Soc. 2005, 127, 8044-8049.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 8044-8049
-
-
Burgos, C.H.1
Canales, E.2
Matos, K.3
Soderquist, J.A.4
-
27
-
-
85022536996
-
-
Catalytic asymmetric carbonyl allylation employing allyl metal reagents: a K. Furuta, M. Mouri, H. Yamamoto, Synlett 1991, 561-562;
-
Catalytic asymmetric carbonyl allylation employing allyl metal reagents: a) K. Furuta, M. Mouri, H. Yamamoto, Synlett 1991, 561-562;
-
-
-
-
28
-
-
12044252883
-
-
b) A. L. Costa, M. G. Piazza, E. Tagliavini, C. Trombini, A. Umani-Ronchi, J. Am. Chem. Soc. 1993, 115, 7001-7002;
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 7001-7002
-
-
Costa, A.L.1
Piazza, M.G.2
Tagliavini, E.3
Trombini, C.4
Umani-Ronchi, A.5
-
29
-
-
0001488391
-
-
c) G. E. Keck, K. H. Tarbet, L. S. Geraci, J. Am. Chem. Soc. 1993, 115, 8467-8468;
-
(1993)
J. Am. Chem. Soc
, vol.115
, pp. 8467-8468
-
-
Keck, G.E.1
Tarbet, K.H.2
Geraci, L.S.3
-
30
-
-
33751157465
-
-
d) S. E. Denmark, D. M. Coe, N. E. Pratt, B. D. Griedel, J. Org. Chem. 1994, 59, 6161-6163;
-
(1994)
J. Org. Chem
, vol.59
, pp. 6161-6163
-
-
Denmark, S.E.1
Coe, D.M.2
Pratt, N.E.3
Griedel, B.D.4
-
32
-
-
4544245462
-
-
For selected reviews covering carbonyl allylation through umpolung of π-allyls, see: a, Eds, E.-i. Negishi, A. de Meijere, Wiley, New York
-
For selected reviews covering carbonyl allylation through umpolung of π-allyls, see: a) Y. Tamaru in Handbook of Organopalladium Chemistry for Organic Synthesis, Vol. 2 (Eds.: E.-i. Negishi, A. de Meijere), Wiley, New York, 2002, pp. 1917-1943;
-
(2002)
Handbook of Organopalladium Chemistry for Organic Synthesis
, vol.2
, pp. 1917-1943
-
-
Tamaru, Y.1
-
35
-
-
0000012889
-
-
For selected examples of reactions involving nucleophilic π-allyls, see: Palladium: a T. Tabuchi, J. Inanaga, M. Yamaguchi, Tetrahedron Lett. 1986, 27, 1195-1196;
-
For selected examples of reactions involving nucleophilic π-allyls, see: Palladium: a) T. Tabuchi, J. Inanaga, M. Yamaguchi, Tetrahedron Lett. 1986, 27, 1195-1196;
-
-
-
-
36
-
-
0000888349
-
-
b) J. P. Takahara, Y. Masuyama, Y. Kurusu, J. Am. Chem. Soc. 1992, 114, 2577-2586;
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 2577-2586
-
-
Takahara, J.P.1
Masuyama, Y.2
Kurusu, Y.3
-
37
-
-
0032541719
-
-
c) M. Kimura, Y. Ogawa, M. Shimizu, M. Sueishi, S. Tanaka, Y. Tamaru, Tetrahedron Lett. 1998, 39, 6903-6906;
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 6903-6906
-
-
Kimura, M.1
Ogawa, Y.2
Shimizu, M.3
Sueishi, M.4
Tanaka, S.5
Tamaru, Y.6
-
38
-
-
4544294704
-
-
d) M. Kimura, M. Shimizu, K. Shibata, M. Tazoe, Y. Tamaru, Angew. Chem. 2003, 115, 3514-3517;
-
(2003)
Angew. Chem
, vol.115
, pp. 3514-3517
-
-
Kimura, M.1
Shimizu, M.2
Shibata, K.3
Tazoe, M.4
Tamaru, Y.5
-
39
-
-
0043031403
-
-
Angew. Chem. Int. Ed. 2003, 42, 3392-3395;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 3392-3395
-
-
-
40
-
-
33744793559
-
-
e) G. Zanoni, S. Gladiali, A. Marchetti, P. Piccinini, I. Tredici, G. Vidari, Angew. Chem. 2004, 116, 864-867;
-
(2004)
Angew. Chem
, vol.116
, pp. 864-867
-
-
Zanoni, G.1
Gladiali, S.2
Marchetti, A.3
Piccinini, P.4
Tredici, I.5
Vidari, G.6
-
41
-
-
2942632388
-
-
Angew. Chem. Int. Ed. 2004, 43, 846-849;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 846-849
-
-
-
42
-
-
8644248155
-
-
Rhodium: f Y. Masuyama, Y. Kaneko, Y. Kurusu, Tetrahedron Lett. 2004, 45, 8969-8971;
-
Rhodium: f) Y. Masuyama, Y. Kaneko, Y. Kurusu, Tetrahedron Lett. 2004, 45, 8969-8971;
-
-
-
-
43
-
-
0002541696
-
-
Ruthenium: g Y. Tsuji, T. Mukai, T. Kondo, Y. Watanabe, J. Organomet. Chem. 1989, 369, C51-C53;
-
Ruthenium: g) Y. Tsuji, T. Mukai, T. Kondo, Y. Watanabe, J. Organomet. Chem. 1989, 369, C51-C53;
-
-
-
-
44
-
-
0000323430
-
-
h) T. Kondo, H. Ono, N. Satake, T.-a. Mitsudo, Y. Watanabe, Organometallics 1995, 14, 1945-1953.
-
(1995)
Organometallics
, vol.14
, pp. 1945-1953
-
-
Kondo, T.1
Ono, H.2
Satake, N.3
Mitsudo, T.-A.4
Watanabe, Y.5
-
45
-
-
0029990032
-
-
For selected examples of carbonyl allylation through catalytic Nozaki-Hiyama-Kishi coupling, see: a
-
For selected examples of carbonyl allylation through catalytic Nozaki-Hiyama-Kishi coupling, see: a) A. Fürstner, N. Shi, J. Am. Chem. Soc. 1996, 118, 2533-2534;
-
(1996)
J. Am. Chem. Soc
, vol.118
, pp. 2533-2534
-
-
Fürstner, A.1
Shi, N.2
-
46
-
-
0034653141
-
-
b) M. Bandini, P. G. Cozzi, A. Umani-Ronchi, Polyhedron 2000, 19, 537-539;
-
(2000)
Polyhedron
, vol.19
, pp. 537-539
-
-
Bandini, M.1
Cozzi, P.G.2
Umani-Ronchi, A.3
-
47
-
-
33645923054
-
-
c) H. A. McManus, P. G. Cozzi, P. J. Guiry, Adv. Synth. Catal. 2006, 348, 551-558;
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 551-558
-
-
McManus, H.A.1
Cozzi, P.G.2
Guiry, P.J.3
-
49
-
-
38549136502
-
-
e) G. C. Hargaden, T. P. O'sullivan, P. J. Guiry, Org. Biomol. Chem. 2008, 6, 562-566.
-
(2008)
Org. Biomol. Chem
, vol.6
, pp. 562-566
-
-
Hargaden, G.C.1
O'sullivan, T.P.2
Guiry, P.J.3
-
50
-
-
36749056768
-
-
For a recent review of catalytic Nozaki-Hiyama-Kishi coupling, see
-
For a recent review of catalytic Nozaki-Hiyama-Kishi coupling, see: G. C. Hargaden, P. J. Guiry, Adv. Synth. Catal. 2007, 349, 2407-2424.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 2407-2424
-
-
Hargaden, G.C.1
Guiry, P.J.2
-
51
-
-
6744264109
-
-
For reviews on carbonyl-ene reactions, see: a
-
For reviews on carbonyl-ene reactions, see: a) K. Mikami, M. Shimizu, Chem. Rev. 1992, 92, 1021-1050;
-
(1992)
Chem. Rev
, vol.92
, pp. 1021-1050
-
-
Mikami, K.1
Shimizu, M.2
-
55
-
-
33646460152
-
-
For nickel catalyzed carbonyl-ene reactions, see: a
-
For nickel catalyzed carbonyl-ene reactions, see: a) C.-Y. Ho, S.-S. Ng, T. F. Jamison, J. Am. Chem. Soc. 2006, 128, 5362-5363;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 5362-5363
-
-
Ho, C.-Y.1
Ng, S.-S.2
Jamison, T.F.3
-
56
-
-
33748340011
-
-
b) S.-S. Ng, C.-Y. Ho, T. F. Jamison, J. Am. Chem. Soc. 2006, 128, 11513-11528.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 11513-11528
-
-
Ng, S.-S.1
Ho, C.-Y.2
Jamison, T.F.3
-
57
-
-
4644336644
-
-
Reviews on hydrogen-mediated C-C coupling: a H.-Y. Jang, M. J. Krische, Acc. Chem. Res. 2004, 37, 653-661;
-
Reviews on hydrogen-mediated C-C coupling: a) H.-Y. Jang, M. J. Krische, Acc. Chem. Res. 2004, 37, 653-661;
-
-
-
-
58
-
-
33846995439
-
-
b) M.-Y. Ngai, J.-R. Kong, M. J. Krische, J. Org. Chem. 2007, 72, 1063-1072;
-
(2007)
J. Org. Chem
, vol.72
, pp. 1063-1072
-
-
Ngai, M.-Y.1
Kong, J.-R.2
Krische, M.J.3
-
60
-
-
38049062493
-
-
d) E. Skucas, M.-Y. Ngai, V. Komanduri, M. J. Krische, Acc. Chem. Res. 2007, 40, 1394-1401;
-
(2007)
Acc. Chem. Res
, vol.40
, pp. 1394-1401
-
-
Skucas, E.1
Ngai, M.-Y.2
Komanduri, V.3
Krische, M.J.4
-
62
-
-
34250817603
-
-
For recent examples, see: C=X Vinylation: a E. Skucas, J. R. Kong, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 7242-7243;
-
For recent examples, see: C=X Vinylation: a) E. Skucas, J. R. Kong, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 7242-7243;
-
-
-
-
63
-
-
34447529183
-
-
b) A. Barchuk, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 8432-8433;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 8432-8433
-
-
Barchuk, A.1
Ngai, M.-Y.2
Krische, M.J.3
-
64
-
-
35548979533
-
-
c) M.-Y. Ngai, A. Barchuk, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 12644-12645.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12644-12645
-
-
Ngai, M.-Y.1
Barchuk, A.2
Krische, M.J.3
-
65
-
-
32644453569
-
-
Aldol and Mannich addition: d C.-K. Jung, S. A. Garner, M. J. Krische, Org. Lett. 2006, 8, 519-522;
-
Aldol and Mannich addition: d) C.-K. Jung, S. A. Garner, M. J. Krische, Org. Lett. 2006, 8, 519-522;
-
-
-
-
68
-
-
40949114623
-
-
g) C. Bee, H. Iida, S. B. Han, A. Hassan, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 2746-2747.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 2746-2747
-
-
Bee, C.1
Iida, H.2
Han, S.B.3
Hassan, A.4
Krische, M.J.5
-
69
-
-
58249103836
-
-
Acyl substitution: h Y.-T. Hong, A. Barchuk, M. J. Krische, Angew. Chem. 2006, 118, 7039-7042;
-
Acyl substitution: h) Y.-T. Hong, A. Barchuk, M. J. Krische, Angew. Chem. 2006, 118, 7039-7042;
-
-
-
-
70
-
-
33750488411
-
-
Angew. Chem. Int. Ed. 2006, 45, 6885-6888.
-
(2006)
Angew. Chem. Int. Ed
, vol.45
, pp. 6885-6888
-
-
-
71
-
-
36049003722
-
-
For reviews of related hydrogen autotransfer processes, which result in formal substitution of the hydroxy moiety rather than carbonyl addition, see: a
-
For reviews of related hydrogen autotransfer processes, which result in formal substitution of the hydroxy moiety rather than carbonyl addition, see: a) G. Guillena, D. J. Ramón, M. Yus, Angew. Chem. 2007, 119, 2410-2416;
-
(2007)
Angew. Chem
, vol.119
, pp. 2410-2416
-
-
Guillena, G.1
Ramón, D.J.2
Yus, M.3
-
72
-
-
34250893845
-
-
Angew. Chem. Int. Ed. 2007, 46, 2358-2364;
-
(2007)
Angew. Chem. Int. Ed
, vol.46
, pp. 2358-2364
-
-
-
73
-
-
34547158082
-
-
b) M. H. S. A. Hamid, P. A. Slatford, J. M. J. Williams, Adv. Synth. Catal. 2007, 349, 1555-1575.
-
(2007)
Adv. Synth. Catal
, vol.349
, pp. 1555-1575
-
-
Hamid, M.H.S.A.1
Slatford, P.A.2
Williams, J.M.J.3
-
74
-
-
23744445162
-
-
Processes that enable the direct catalytic functionalization of carbinol C-H bonds are highly uncommon. For an isolated report, see: L. Shi, Y.-Q. Tu, M. Wang, F.-M. Zhang, C.-A. Fan, Y.-M. Zhao, W. J. Xia, J. Am. Chem. Soc. 2005, 127, 10836-10837
-
Processes that enable the direct catalytic functionalization of carbinol C-H bonds are highly uncommon. For an isolated report, see: L. Shi, Y.-Q. Tu, M. Wang, F.-M. Zhang, C.-A. Fan, Y.-M. Zhao, W. J. Xia, J. Am. Chem. Soc. 2005, 127, 10836-10837.
-
-
-
-
75
-
-
35548993714
-
-
E. Skucas, J. F. Bower, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 12678-12679.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 12678-12679
-
-
Skucas, E.1
Bower, J.F.2
Krische, M.J.3
-
76
-
-
37049007450
-
-
J. F. Bower, E. Skucas, R. L. Patman, M. J. Krische, J. Am. Chem. Soc. 2007, 129, 15134-15135.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 15134-15135
-
-
Bower, J.F.1
Skucas, E.2
Patman, R.L.3
Krische, M.J.4
-
78
-
-
4243378570
-
-
For selected reviews of ruthenium catalyzed transfer hydrogenation, see: a
-
For selected reviews of ruthenium catalyzed transfer hydrogenation, see: a) G. Zassinovich, G. Mestroni, S. Gladiali, Chem. Rev. 1992, 92, 1051-1069;
-
(1992)
Chem. Rev
, vol.92
, pp. 1051-1069
-
-
Zassinovich, G.1
Mestroni, G.2
Gladiali, S.3
-
80
-
-
0035977261
-
-
c) R. Noyori, M. Yamakawa, S. Hashiguchi, J. Org. Chem. 2001, 66, 7931-7944;
-
(2001)
J. Org. Chem
, vol.66
, pp. 7931-7944
-
-
Noyori, R.1
Yamakawa, M.2
Hashiguchi, S.3
-
83
-
-
0001552544
-
-
e) R. Noyori, Angew. Chem. 2002, 114, 2108-2123;
-
(2002)
Angew. Chem
, vol.114
, pp. 2108-2123
-
-
Noyori, R.1
-
84
-
-
0037124885
-
-
Angew. Chem. Int. Ed. 2002, 41, 2008-2022;
-
(2002)
Angew. Chem. Int. Ed
, vol.41
, pp. 2008-2022
-
-
-
86
-
-
33646442062
-
-
g) K. Muñiz, Angew. Chem. 2005, 117, 6780-6785;
-
(2005)
Angew. Chem
, vol.117
, pp. 6780-6785
-
-
Muñiz, K.1
-
87
-
-
27444437031
-
-
Angew. Chem. Int. Ed. 2005, 44, 6622-6627;
-
(2005)
Angew. Chem. Int. Ed
, vol.44
, pp. 6622-6627
-
-
-
91
-
-
0000000669
-
-
For a review of ruthenium catalyzed alkene hydroformylation, see
-
For a review of ruthenium catalyzed alkene hydroformylation, see: P. Kalck, Y. Peres, J. Jenck, Adv. Organomet. Chem. 1991, 32, 121-146.
-
(1991)
Adv. Organomet. Chem
, vol.32
, pp. 121-146
-
-
Kalck, P.1
Peres, Y.2
Jenck, J.3
-
92
-
-
4143079031
-
-
Also see references [6g,h, For ruthenium catalyzed reductive C-C bond formations beyond alkene hydroformylation, see
-
For ruthenium catalyzed reductive C-C bond formations beyond alkene hydroformylation, see: C.-M. Yu, S. Lee, Y.-T. Hong, S.-K. Yoon, Tetrahedron Lett. 2004, 45, 6557-6561. Also see references [6g,h].
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 6557-6561
-
-
Yu, C.-M.1
Lee, S.2
Hong, Y.-T.3
Yoon, S.-K.4
-
93
-
-
0035385137
-
-
For selected reviews of ruthenium catalyzed C-C coupling, see: a
-
For selected reviews of ruthenium catalyzed C-C coupling, see: a) B. M. Trost, F. D. Toste, A. B. Pinkerton, Chem. Rev. 2001, 101, 2067-2096;
-
(2001)
Chem. Rev
, vol.101
, pp. 2067-2096
-
-
Trost, B.M.1
Toste, F.D.2
Pinkerton, A.B.3
-
95
-
-
27144514071
-
-
c) S. Derien, F. Monnier, P. H. Dixneuf, Top. Organomet. Chem. 2004, 11, 1-44.
-
(2004)
Top. Organomet. Chem
, vol.11
, pp. 1-44
-
-
Derien, S.1
Monnier, F.2
Dixneuf, P.H.3
-
96
-
-
51649085840
-
-
M.-Y. Ngai, E. Skucas, M. J. Krische, Org. Lett. 2008, 10, 2705-2708.
-
(2008)
Org. Lett
, vol.10
, pp. 2705-2708
-
-
Ngai, M.-Y.1
Skucas, E.2
Krische, M.J.3
-
97
-
-
43549090940
-
-
J. F. Bower, R. L. Patman, M. J. Krische, Org. Lett. 2008, 10, 1033-1035.
-
(2008)
Org. Lett
, vol.10
, pp. 1033-1035
-
-
Bower, J.F.1
Patman, R.L.2
Krische, M.J.3
-
98
-
-
58249117595
-
-
For a related rhodium-catalyzed cyclohexadiene-aldehyde reductive coupling employing elemental hydrogen as the terminal reductant, see: H.-Y. Jang, R. R. Huddleston, M. J. Krische, Angew. Chem. 2003, 115, 4208-4211;
-
For a related rhodium-catalyzed cyclohexadiene-aldehyde reductive coupling employing elemental hydrogen as the terminal reductant, see: H.-Y. Jang, R. R. Huddleston, M. J. Krische, Angew. Chem. 2003, 115, 4208-4211;
-
-
-
-
99
-
-
0141649629
-
-
Angew. Chem. Int. Ed. 2003, 42, 4074-4077.
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 4074-4077
-
-
-
100
-
-
43949117421
-
-
a) F. Shibahara, J. F. Bower, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 6338-6339;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 6338-6339
-
-
Shibahara, F.1
Bower, J.F.2
Krische, M.J.3
-
101
-
-
54849406161
-
-
b) F. Shibahara, J. F. Bower, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 14120-14122.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 14120-14122
-
-
Shibahara, F.1
Bower, J.F.2
Krische, M.J.3
-
102
-
-
0000972326
-
-
For a related ruthenium catalyzed hydroacylation of 1,3-dienes employing aldehydes as acyl donors, see
-
For a related ruthenium catalyzed hydroacylation of 1,3-dienes employing aldehydes as acyl donors, see: T. Kondo, N. Hiraishi, Y. Morisaki, K. Wada, Y. Watanabe, T-a. Mitsudo, Organometallics 1998, 17, 2131-2134.
-
(1998)
Organometallics
, vol.17
, pp. 2131-2134
-
-
Kondo, T.1
Hiraishi, N.2
Morisaki, Y.3
Wada, K.4
Watanabe, Y.5
Mitsudo, T.-A.6
-
103
-
-
0032577043
-
-
For intermolecular nickel-catalyzed diene-aldehyde reductive coupling, see: a
-
For intermolecular nickel-catalyzed diene-aldehyde reductive coupling, see: a) M. Kimura, A. Ezoe, K. Shibata, Y. Tamaru, J. Am. Chem. Soc. 1998, 120, 4033-4034;
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 4033-4034
-
-
Kimura, M.1
Ezoe, A.2
Shibata, K.3
Tamaru, Y.4
-
104
-
-
0032543491
-
-
b) M. Takimoto, Y. Hiraga, Y. Sato, M. Mori, Tetrahedron Lett. 1998, 39, 4543-4546;
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 4543-4546
-
-
Takimoto, M.1
Hiraga, Y.2
Sato, Y.3
Mori, M.4
-
105
-
-
0001399137
-
-
c) M. Kimura, H. Fujimatsu, A. Ezoe, K. Shibata, M. Shimizu, S. Matsumoto, Y. Tamaru, Angew. Chem. 1999, 111, 410-413;
-
(1999)
Angew. Chem
, vol.111
, pp. 410-413
-
-
Kimura, M.1
Fujimatsu, H.2
Ezoe, A.3
Shibata, K.4
Shimizu, M.5
Matsumoto, S.6
Tamaru, Y.7
-
106
-
-
0033082780
-
-
Angew. Chem. Int. Ed. 1999, 38, 397-400;
-
(1999)
Angew. Chem. Int. Ed
, vol.38
, pp. 397-400
-
-
-
107
-
-
0034718352
-
-
d) M. Kimura, K. Shibata, Y. Koudahashi, Y. Tamaru, Tetrahedron Lett. 2000, 41, 6789-6793;
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 6789-6793
-
-
Kimura, M.1
Shibata, K.2
Koudahashi, Y.3
Tamaru, Y.4
-
108
-
-
0013112163
-
-
e) M. Kimura, A. Ezoe, S. Tanaka, Y. Tamaru, Angew. Chem. 2001, 113, 3712-3714;
-
(2001)
Angew. Chem
, vol.113
, pp. 3712-3714
-
-
Kimura, M.1
Ezoe, A.2
Tanaka, S.3
Tamaru, Y.4
-
109
-
-
0035476966
-
-
Angew. Chem. Int. Ed. 2001, 40, 3600-3602;
-
(2001)
Angew. Chem. Int. Ed
, vol.40
, pp. 3600-3602
-
-
-
110
-
-
0043192557
-
-
f) T.-P. Loh, H.-Y. Song, Y. Zhou, Org. Lett. 2002, 4, 2715-2717;
-
(2002)
Org. Lett
, vol.4
, pp. 2715-2717
-
-
Loh, T.-P.1
Song, H.-Y.2
Zhou, Y.3
-
111
-
-
0037039891
-
-
g) Y. Sato, R. Sawaki, N. Saito, M. Mori, J. Org. Chem. 2002, 67, 656-662;
-
(2002)
J. Org. Chem
, vol.67
, pp. 656-662
-
-
Sato, Y.1
Sawaki, R.2
Saito, N.3
Mori, M.4
-
113
-
-
33745728204
-
-
i) M. Kimura, A. Ezoe, M. Mori, K. Iwata, Y. Tamaru, J. Am. Chem. Soc. 2006, 128, 8559-8568;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 8559-8568
-
-
Kimura, M.1
Ezoe, A.2
Mori, M.3
Iwata, K.4
Tamaru, Y.5
-
114
-
-
33847652798
-
-
j) Y. Yang, S.-F. Zhu, H.-F. Duan, C.-Y. Zhou, L.-X. Wang, Q.-L. Zhou, J. Am. Chem. Soc. 2007, 129, 2248-2249;
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 2248-2249
-
-
Yang, Y.1
Zhu, S.-F.2
Duan, H.-F.3
Zhou, C.-Y.4
Wang, L.-X.5
Zhou, Q.-L.6
-
115
-
-
38349171275
-
-
k) Y. Sato, Y. Hinata, R. Seki, Y. Oonishi, N. Saito, Org. Lett. 2007, 9, 5597-5599.
-
(2007)
Org. Lett
, vol.9
, pp. 5597-5599
-
-
Sato, Y.1
Hinata, Y.2
Seki, R.3
Oonishi, Y.4
Saito, N.5
-
116
-
-
0001374863
-
-
For reviews encompassing nickel-catalyzed diene-aldehyde reductive coupling, see: a
-
For reviews encompassing nickel-catalyzed diene-aldehyde reductive coupling, see: a) Y. Tamaru, J. Organomet. Chem. 1999, 576, 215-231;
-
(1999)
J. Organomet. Chem
, vol.576
, pp. 215-231
-
-
Tamaru, Y.1
-
117
-
-
4544271454
-
-
b) S.-i. Ikeda, Angew. Chem. 2003, 115, 5276-5278;
-
(2003)
Angew. Chem
, vol.115
, pp. 5276-5278
-
-
Ikeda, S.-I.1
-
118
-
-
0242467768
-
-
Angew. Chem. Int. Ed. 2003, 42, 5120-5122;
-
(2003)
Angew. Chem. Int. Ed
, vol.42
, pp. 5120-5122
-
-
-
120
-
-
4544323639
-
-
Angew. Chem. Int. Ed. 2004, 43, 3890-3908;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 3890-3908
-
-
-
121
-
-
84891322500
-
-
Ed, Y. Tamaru, Wiley-VCH, Weinheim
-
d) Modern Organo Nickel Chemistry (Ed.: Y. Tamaru), Wiley-VCH, Weinheim, 2005;
-
(2005)
Modern Organo Nickel Chemistry
-
-
-
124
-
-
0000833640
-
-
T. Kondo, T. Mukai, Y. Watanabe, J. Org. Chem. 1991, 56, 487-489.
-
(1991)
J. Org. Chem
, vol.56
, pp. 487-489
-
-
Kondo, T.1
Mukai, T.2
Watanabe, Y.3
-
125
-
-
0242500920
-
-
a) F. Lopez, T. Ohmura, J. F. Hartwig, J. Am. Chem. Soc. 2003, 125, 3426-3427;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 3426-3427
-
-
Lopez, F.1
Ohmura, T.2
Hartwig, J.F.3
-
126
-
-
2442584444
-
-
b) H. Nakagawa, T. Hirabayashi, S. Sakaguchi, Y. Ishii, J. Org. Chem. 2004, 69, 3474-3477;
-
(2004)
J. Org. Chem
, vol.69
, pp. 3474-3477
-
-
Nakagawa, H.1
Hirabayashi, T.2
Sakaguchi, S.3
Ishii, Y.4
-
128
-
-
4644229326
-
-
Angew. Chem. Int. Ed. 2004, 43, 4794-4797;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 4794-4797
-
-
-
131
-
-
41949120990
-
-
Angew. Chem. Int. Ed. 2008, 47, 1928-1931.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 1928-1931
-
-
-
132
-
-
43949139260
-
-
a) I. S. Kim, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 6340-6341;
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 6340-6341
-
-
Kim, I.S.1
Ngai, M.-Y.2
Krische, M.J.3
-
133
-
-
55549119981
-
-
b) I. S. Kim, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2008, 130, 14891-14899.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 14891-14899
-
-
Kim, I.S.1
Ngai, M.-Y.2
Krische, M.J.3
-
134
-
-
0003627206
-
-
For reviews encompassing carbonyl propargylation employing allenyl metal reagents, see: a, Ed, S. Patai, Wiley, New York
-
For reviews encompassing carbonyl propargylation employing allenyl metal reagents, see: a) J.-L. Moreau in The Chemistry of Ketenes, Allenes and Related Compounds (Ed.: S. Patai), Wiley, New York, 1980, pp. 363-413;
-
(1980)
The Chemistry of Ketenes, Allenes and Related Compounds
, pp. 363-413
-
-
Moreau, J.-L.1
-
136
-
-
27644550194
-
-
c) B. W. Gung, Org. React. 2004, 64, 1-113;
-
(2004)
Org. React
, vol.64
, pp. 1-113
-
-
Gung, B.W.1
-
137
-
-
33744983663
-
-
Eds, N. Krause, A. S. K. Hashmi, Wiley-VCH, Weinheim
-
d) J. A. Marshall, B. W. Gung, M. L. Grachan in Modern Allene Chemistry (Eds.: N. Krause, A. S. K. Hashmi), Wiley-VCH, Weinheim, 2004, pp. 493-592;
-
(2004)
Modern Allene Chemistry
, pp. 493-592
-
-
Marshall, J.A.1
Gung, B.W.2
Grachan, M.L.3
-
139
-
-
0000705244
-
-
For selected milestones in carbonyl propargylation, see: a
-
For selected milestones in carbonyl propargylation, see: a) C. Prévost, M. Gaudemar, J. Honigberg, C. R. Hebd. Seances Acad. Sci. 1950, 230, 1186-1188;
-
(1950)
C. R. Hebd. Seances Acad. Sci
, vol.230
, pp. 1186-1188
-
-
Prévost, C.1
Gaudemar, M.2
Honigberg, J.3
-
141
-
-
0344973614
-
-
c) M. Karila, M. L. Capmau, W. Chodkiewicz, C. R. Hebd. Seances Acad. Sci. 1969, 269, 342-345;
-
(1969)
C. R. Hebd. Seances Acad. Sci
, vol.269
, pp. 342-345
-
-
Karila, M.1
Capmau, M.L.2
Chodkiewicz, W.3
-
146
-
-
0000564079
-
-
h) R. Haruta, M. Ishiguro, N. Ikeda, H. Yamamoto, J. Am. Chem. Soc. 1982, 104, 7667-7669;
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 7667-7669
-
-
Haruta, R.1
Ishiguro, M.2
Ikeda, N.3
Yamamoto, H.4
-
147
-
-
0025374143
-
-
i) E. J. Corey, C.-M. Yu, D.-H. Lee, J. Am. Chem. Soc. 1990, 112, 878-879;
-
(1990)
J. Am. Chem. Soc
, vol.112
, pp. 878-879
-
-
Corey, E.J.1
Yu, C.-M.2
Lee, D.-H.3
-
151
-
-
37049072134
-
-
m) Y. Matsumoto, M. Naito, Y. Uozumi, T. Hayashi, J. Chem. Soc. Chem. Commun. 1993, 1468-1469;
-
(1993)
J. Chem. Soc. Chem. Commun
, pp. 1468-1469
-
-
Matsumoto, Y.1
Naito, M.2
Uozumi, Y.3
Hayashi, T.4
-
152
-
-
0028053497
-
-
n) G. E. Keck, D. Krishnamurthy, X. Chen, . Tetrahedron Lett. 1994, 35, 8323-8324;
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 8323-8324
-
-
Keck, G.E.1
Krishnamurthy, D.2
Chen, X.3
-
154
-
-
1842788947
-
-
For rhodium catalyzed reductive coupling of 1,3-enynes to carbonyl compounds and imines, see: a
-
For rhodium catalyzed reductive coupling of 1,3-enynes to carbonyl compounds and imines, see: a) H.-Y. Jang, R. R. Huddleston, M. J. Krische, J. Am. Chem. Soc. 2004, 126, 4664-4668;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4664-4668
-
-
Jang, H.-Y.1
Huddleston, R.R.2
Krische, M.J.3
-
155
-
-
23844494674
-
-
b) J.-R. Kong, C.-W. Cho, M. J. Krische, J. Am. Chem. Soc. 2005, 127, 11269-11276;
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 11269-11276
-
-
Kong, J.-R.1
Cho, C.-W.2
Krische, M.J.3
-
156
-
-
31444453628
-
-
c) J.-R. Kong, M.-Y. Ngai, M. J. Krische, J. Am. Chem. Soc. 2006, 128, 718-719;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 718-719
-
-
Kong, J.-R.1
Ngai, M.-Y.2
Krische, M.J.3
-
158
-
-
34848878354
-
-
e) Y.-T. Hong, C.-W. Cho, E. Skucas, M. J. Krische, Org. Lett. 2007, 9, 3745-3748.
-
(2007)
Org. Lett
, vol.9
, pp. 3745-3748
-
-
Hong, Y.-T.1
Cho, C.-W.2
Skucas, E.3
Krische, M.J.4
-
159
-
-
1842607439
-
-
For nickel catalyzed reductive coupling of 1,3-enynes to carbonyl compounds, see: a
-
For nickel catalyzed reductive coupling of 1,3-enynes to carbonyl compounds, see: a) K. M. Miller, T. Luanphaisarnnont, C. Molinaro, T. F. Jamison, J. Am. Chem. Soc. 2004, 126, 4130-4131;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 4130-4131
-
-
Miller, K.M.1
Luanphaisarnnont, T.2
Molinaro, C.3
Jamison, T.F.4
-
161
-
-
27544515916
-
-
c) K. M. Miller, E. A. Colby, K. S. Woodin, T. F. Jamison, Adv. Synth. Catal. 2005, 347, 1533-1536.
-
(2005)
Adv. Synth. Catal
, vol.347
, pp. 1533-1536
-
-
Miller, K.M.1
Colby, E.A.2
Woodin, K.S.3
Jamison, T.F.4
-
162
-
-
58249100972
-
-
For seminal contributions to nickel catalyzed alkyne-carbonyl reductive coupling, see reference [45a
-
For seminal contributions to nickel catalyzed alkyne-carbonyl reductive coupling, see reference [45a].
-
-
-
-
163
-
-
11244320756
-
-
For reviews encompassing nickel catalyzed alkyne-carbonyl reductive coupling, see: a
-
For reviews encompassing nickel catalyzed alkyne-carbonyl reductive coupling, see: a) J. Montgomery, Angew. Chem. 2004, 116, 3980-3998;
-
(2004)
Angew. Chem
, vol.116
, pp. 3980-3998
-
-
Montgomery, J.1
-
164
-
-
4544323639
-
-
Angew. Chem. Int. Ed. 2004, 43, 3890-3908;
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 3890-3908
-
-
-
167
-
-
58249094810
-
-
R. L. Patman, V. M. Williams, J. F. Bower, M. J. Krische, Angew. Chem. 2008, 120, 5298-5301;
-
(2008)
Angew. Chem
, vol.120
, pp. 5298-5301
-
-
Patman, R.L.1
Williams, V.M.2
Bower, J.F.3
Krische, M.J.4
-
168
-
-
48149091798
-
-
Angew. Chem. Int. Ed. 2008, 47, 5220-5223.
-
(2008)
Angew. Chem. Int. Ed
, vol.47
, pp. 5220-5223
-
-
-
170
-
-
33845373528
-
-
b) M. Kitamura, S. Suga, K. Kawai, R. Noyori, J. Am. Chem. Soc. 1986, 108, 6071-6072.
-
(1986)
J. Am. Chem. Soc
, vol.108
, pp. 6071-6072
-
-
Kitamura, M.1
Suga, S.2
Kawai, K.3
Noyori, R.4
-
171
-
-
84987584214
-
-
For enantioselective catalytic addition of vinylzinc reagents to aldehydes, see: a
-
For enantioselective catalytic addition of vinylzinc reagents to aldehydes, see: a) W. Oppolzer, R. N. Radinov, Helv. Chim. Acta 1992, 75, 170-173;
-
(1992)
Helv. Chim. Acta
, vol.75
, pp. 170-173
-
-
Oppolzer, W.1
Radinov, R.N.2
-
175
-
-
0028924320
-
-
e) W. Oppolzer, R. N. Radinov, J. De Brabander, Tetrahedron Lett. 1995, 36, 2607-2610;
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 2607-2610
-
-
Oppolzer, W.1
Radinov, R.N.2
De Brabander, J.3
-
177
-
-
0035854288
-
-
g) W. Oppolzer, R. N. Radinov, E. El-Sayed, J. Org. Chem. 2001, 66, 4766-4770;
-
(2001)
J. Org. Chem
, vol.66
, pp. 4766-4770
-
-
Oppolzer, W.1
Radinov, R.N.2
El-Sayed, E.3
-
179
-
-
0037120811
-
-
i) Y. K. Chen, A. E. Lurain, P. J. Walsh, J. Am. Chem. Soc. 2002, 124, 12225-12231;
-
(2002)
J. Am. Chem. Soc
, vol.124
, pp. 12225-12231
-
-
Chen, Y.K.1
Lurain, A.E.2
Walsh, P.J.3
-
180
-
-
0037458974
-
-
j) J.-X. Ji, L.-Q. Qiu, C. W. Yip, A. S. C. Chan, J. Org. Chem. 2003, 68, 1589-1590;
-
(2003)
J. Org. Chem
, vol.68
, pp. 1589-1590
-
-
Ji, J.-X.1
Qiu, L.-Q.2
Yip, C.W.3
Chan, A.S.C.4
-
182
-
-
1642503212
-
-
l) D.-H. Ko, S.-W. Kang, K. H. Kim, Y. Chung, D.-C. Ha, Bull. Korean Chem. Soc. 2004, 25, 35-36;
-
(2004)
Bull. Korean Chem. Soc
, vol.25
, pp. 35-36
-
-
Ko, D.-H.1
Kang, S.-W.2
Kim, K.H.3
Chung, Y.4
Ha, D.-C.5
-
183
-
-
4644274423
-
-
m) C. M. Sprout, M. L. Richmond, C. T. Seto, J. Org. Chem. 2004, 69, 6666-6673;
-
(2004)
J. Org. Chem
, vol.69
, pp. 6666-6673
-
-
Sprout, C.M.1
Richmond, M.L.2
Seto, C.T.3
-
184
-
-
18844416365
-
-
n) S.-J. Jeon, Y. K. Chen, P. J. Walsh, Org. Lett. 2005, 7, 1729-1732;
-
(2005)
Org. Lett
, vol.7
, pp. 1729-1732
-
-
Jeon, S.-J.1
Chen, Y.K.2
Walsh, P.J.3
-
185
-
-
33750499995
-
-
o) F. Lauterwasser, J. Gall, S. Höfener, S. Bräse, Adv. Synth. Catal. 2006, 348, 2068-2074;
-
(2006)
Adv. Synth. Catal
, vol.348
, pp. 2068-2074
-
-
Lauterwasser, F.1
Gall, J.2
Höfener, S.3
Bräse, S.4
-
186
-
-
33746618811
-
-
p) S.-J. Jeon, E. L. Fisher, P. J. Carroll, P. J. Walsh, J. Am. Chem. Soc. 2006, 128, 9618-9619;
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 9618-9619
-
-
Jeon, S.-J.1
Fisher, E.L.2
Carroll, P.J.3
Walsh, P.J.4
-
187
-
-
37549059608
-
-
q) L. Salvi, S.-J. Jeon, E. L. Fisher, P. J. Carroll, P. J. Walsh, J. Am. Chem. Soc. 2007, 129, 16119-16125.
-
(2007)
J. Am. Chem. Soc
, vol.129
, pp. 16119-16125
-
-
Salvi, L.1
Jeon, S.-J.2
Fisher, E.L.3
Carroll, P.J.4
Walsh, P.J.5
-
188
-
-
0037090420
-
-
For reviews encompassing catalytic enantioselective aldehyde vinylation using organozinc reagents, see: a
-
For reviews encompassing catalytic enantioselective aldehyde vinylation using organozinc reagents, see: a) P. Wipf, C. Kendall, Chem. Eur. J. 2002, 8, 1778-1784;
-
(2002)
Chem. Eur. J
, vol.8
, pp. 1778-1784
-
-
Wipf, P.1
Kendall, C.2
-
190
-
-
2542622015
-
-
For catalytic enantioselective ketone vinylation using organozinc reagents, see: a
-
For catalytic enantioselective ketone vinylation using organozinc reagents, see: a) H. Li, P. J. Walsh, J. Am. Chem. Soc. 2004, 126, 6538-6539;
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 6538-6539
-
-
Li, H.1
Walsh, P.J.2
-
192
-
-
12344275269
-
-
c) S.-J. Jeon, H. Li, C. García, L. K. LaRochelle, P. J. Walsh, J. Org. Chem. 2005, 70, 448-455.
-
(2005)
J. Org. Chem
, vol.70
, pp. 448-455
-
-
Jeon, S.-J.1
Li, H.2
García, C.3
LaRochelle, L.K.4
Walsh, P.J.5
-
193
-
-
0010156139
-
-
I. Ojima, M. Tzamarioudaki, C.-Y. Tsai, J. Am. Chem. Soc. 1994, 116, 3643-3644.
-
(1994)
J. Am. Chem. Soc
, vol.116
, pp. 3643-3644
-
-
Ojima, I.1
Tzamarioudaki, M.2
Tsai, C.-Y.3
-
195
-
-
0000944975
-
-
For an aligned study, see
-
b) For an aligned study, see: N. M. Kablaoui, S. L. Buchwald, J. Am. Chem. Soc. 1995, 117, 6785-6786.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 6785-6786
-
-
Kablaoui, N.M.1
Buchwald, S.L.2
-
196
-
-
0030861563
-
-
For intramolecular nickel catalyzed alkyne-carbonyl reductive coupling, see: a
-
For intramolecular nickel catalyzed alkyne-carbonyl reductive coupling, see: a) E. Oblinger, J. Montgomery, J. Am. Chem. Soc. 1997, 119, 9065-9066;
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 9065-9066
-
-
Oblinger, E.1
Montgomery, J.2
-
199
-
-
25444480800
-
-
d) B. Knapp-Reed, G. M. Mahandru, J. Montgomery, J. Am. Chem. Soc. 2005, 127, 13156-13157.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 13156-13157
-
-
Knapp-Reed, B.1
Mahandru, G.M.2
Montgomery, J.3
-
200
-
-
0000524458
-
-
For intermolecular nickel catalyzed alkyne-carbonyl reductive coupling, see: a
-
For intermolecular nickel catalyzed alkyne-carbonyl reductive coupling, see: a) W.-S. Huang, J. Chan, T. F. Jamison, Org. Lett. 2000, 2, 4221-4223;
-
(2000)
Org. Lett
, vol.2
, pp. 4221-4223
-
-
Huang, W.-S.1
Chan, J.2
Jamison, T.F.3
-
201
-
-
0037467387
-
-
b) K. M. Miller, W.-S. Huang, T. F. Jamison, J. Am. Chem. Soc. 2003, 125, 3442-3443;
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 3442-3443
-
-
Miller, K.M.1
Huang, W.-S.2
Jamison, T.F.3
-
202
-
-
0037538818
-
-
c) K. Takai, S. Sakamoto, T. Isshiki, Org. Lett. 2003, 5, 653-655;
-
(2003)
Org. Lett
, vol.5
, pp. 653-655
-
-
Takai, K.1
Sakamoto, S.2
Isshiki, T.3
-
203
-
-
1642354777
-
-
d) G. M. Mahandru, G. Liu, J. Montgomery, J. Am. Chem. Soc. 2004, 126, 3698-3699.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 3698-3699
-
-
Mahandru, G.M.1
Liu, G.2
Montgomery, J.3
|