-
2
-
-
0242595741
-
-
Balme, G., Bossharth, E., and Monteiro, N. Eur. J. Org. Chem. 2003, 4101
-
(2003)
Eur. J. Org. Chem.
, pp. 4101
-
-
Balme, G.1
Bossharth, E.2
Monteiro, N.3
-
3
-
-
22944485617
-
-
Ma, S. Chem. Rev. 2005, 105, 2829
-
(2005)
Chem. Rev.
, vol.105
, pp. 2829
-
-
Ma, S.1
-
5
-
-
23644461773
-
-
Hopkins, C. D., Guan, L., and Malinakova, H. C. J. Org. Chem. 2005, 70, 6848
-
(2005)
J. Org. Chem.
, vol.70
, pp. 6848
-
-
Hopkins, C.D.1
Guan, L.2
Malinakova, H.C.3
-
7
-
-
34249107333
-
-
Bai, T., Ma, S., and Jia, G. Tetrahedron 2007, 63, 6210
-
(2007)
Tetrahedron
, vol.63
, pp. 6210
-
-
Bai, T.1
Ma, S.2
Jia, G.3
-
9
-
-
77954290321
-
-
Catalytic three-component couplings involving allenes, aryl halides, and carbonyls in the presence of In metal
-
Catalytic three-component couplings involving allenes, aryl halides, and carbonyls in the presence of In metal
-
-
-
-
10
-
-
0034696895
-
-
Anwar, U., Grigg, R., Rasparini, M., Savic, V., and Sridharan, V. Chem. Commun. 2000, 645
-
(2000)
Chem. Commun.
, pp. 645
-
-
Anwar, U.1
Grigg, R.2
Rasparini, M.3
Savic, V.4
Sridharan, V.5
-
11
-
-
0037077013
-
-
Kang, S.-K., Lee, S.-W., Jung, J., and Lim, Y. J. Org. Chem. 2002, 67, 4376
-
(2002)
J. Org. Chem.
, vol.67
, pp. 4376
-
-
Kang, S.-K.1
Lee, S.-W.2
Jung, J.3
Lim, Y.4
-
12
-
-
0036080602
-
-
Cooper, I. R., Grigg, R., MacLachlan, W. S., and Sridharan, V. Chem. Commun. 2002, 1372
-
(2002)
Chem. Commun.
, pp. 1372
-
-
Cooper, I.R.1
Grigg, R.2
MacLachlan, W.S.3
Sridharan, V.4
-
13
-
-
77954247683
-
-
Catalytic two-component allene-carbonyl reductive coupling via hydrogenation for diversity-oriented efficient synthesis of homoallyl alchohols:
-
Catalytic two-component allene-carbonyl reductive coupling via hydrogenation for diversity-oriented efficient synthesis of homoallyl alchohols:
-
-
-
-
14
-
-
35548993714
-
-
Skucas, E., Bower, J. F., and Krische, M. J. J. Am. Chem. Soc. 2007, 129, 12678
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 12678
-
-
Skucas, E.1
Bower, J.F.2
Krische, M.J.3
-
15
-
-
37049007450
-
-
Bower, J. F., Skucas, E., Patman, R. L., and Krische, M. J. J. Am. Chem. Soc. 2007, 129, 15134
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 15134
-
-
Bower, J.F.1
Skucas, E.2
Patman, R.L.3
Krische, M.J.4
-
16
-
-
67849092737
-
-
Skucas, E., Zbieg, J. R., and Krische, M. J. J. Am. Chem. Soc. 2009, 131, 5054
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5054
-
-
Skucas, E.1
Zbieg, J.R.2
Krische, M.J.3
-
17
-
-
70149095459
-
-
Han, S. B., Kim, I. S., Han, H., and Krische, M. J. J. Am. Chem. Soc. 2009, 131, 6916
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 6916
-
-
Han, S.B.1
Kim, I.S.2
Han, H.3
Krische, M.J.4
-
18
-
-
77954255868
-
-
Recent examples of transition-metal-catalyzed carbozincation of alkynes: Ni
-
Recent examples of transition-metal-catalyzed carbozincation of alkynes: Ni
-
-
-
-
19
-
-
0032510182
-
-
Stüdemann, T., Ibrahim-Ouali, M., and Knochel, P. Tetrahedron 1998, 54, 1299
-
(1998)
Tetrahedron
, vol.54
, pp. 1299
-
-
Stüdemann, T.1
Ibrahim-Ouali, M.2
Knochel, P.3
-
21
-
-
33750305101
-
-
Shintani, R., Yamagami, T., and Hayashi, T. Org. Lett. 2006, 8, 4799
-
(2006)
Org. Lett.
, vol.8
, pp. 4799
-
-
Shintani, R.1
Yamagami, T.2
Hayashi, T.3
-
22
-
-
70349881440
-
-
Gourdet, B., Rudkin, M. E., Watts, C. A., and Lam, H. W. J. Org. Chem. 2009, 74, 7849
-
(2009)
J. Org. Chem.
, vol.74
, pp. 7849
-
-
Gourdet, B.1
Rudkin, M.E.2
Watts, C.A.3
Lam, H.W.4
-
23
-
-
0141517629
-
-
Maezaki, N., Sawamoto, H., Yoshigami, R., Suzuki, T., and Tanaka, T. Org. Lett. 2003, 5, 1345
-
(2003)
Org. Lett.
, vol.5
, pp. 1345
-
-
Maezaki, N.1
Sawamoto, H.2
Yoshigami, R.3
Suzuki, T.4
Tanaka, T.5
-
24
-
-
34147189535
-
-
Sklute, G., Bolm, C., and Marek, I. Org. Lett. 2007, 9, 1259
-
(2007)
Org. Lett.
, vol.9
, pp. 1259
-
-
Sklute, G.1
Bolm, C.2
Marek, I.3
-
25
-
-
67849133453
-
-
Tarwade, V., Liu, X., Yan, N., and Fox, J. M. J. Am. Chem. Soc. 2009, 131, 5382
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 5382
-
-
Tarwade, V.1
Liu, X.2
Yan, N.3
Fox, J.M.4
-
27
-
-
0034624407
-
-
Fe Nakamura, M., Hirai, A., and Nakamura, E. J. Am. Chem. Soc. 2000, 122, 978
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 978
-
-
Fe Nakamura, M.1
Hirai, A.2
Nakamura, E.3
-
28
-
-
33750622957
-
-
Co Yasui, H., Nishikawa, T., Yorimitsu, H., and Oshima, K. Bull. Chem. Soc. Jpn. 2006, 79, 1271
-
(2006)
Bull. Chem. Soc. Jpn.
, vol.79
, pp. 1271
-
-
Co Yasui, H.1
Nishikawa, T.2
Yorimitsu, H.3
Oshima, K.4
-
29
-
-
66149160252
-
-
Murakami, K., Yorimitsu, H., and Oshima, K. Org. Lett. 2009, 11, 2373
-
(2009)
Org. Lett.
, vol.11
, pp. 2373
-
-
Murakami, K.1
Yorimitsu, H.2
Oshima, K.3
-
31
-
-
33644650016
-
-
Rhodium-catalyzed hydroarylation of allenes with arylboronic acids proceeds via direct protonation of the resulting allylrhodium without transmetalation between the allylrhodium and arylboronic acid
-
Rhodium-catalyzed hydroarylation of allenes with arylboronic acids proceeds via direct protonation of the resulting allylrhodium without transmetalation between the allylrhodium and arylboronic acid: Nishimura, T., Hirabayashi, S., Yasuhara, Y., and Hayashi, T. J. Am. Chem. Soc. 2006, 128, 2556
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 2556
-
-
Nishimura, T.1
Hirabayashi, S.2
Yasuhara, Y.3
Hayashi, T.4
-
32
-
-
34250882833
-
-
Copper-catalyzed conjugate addition of organozinc reagents to reactive allenic esters providing zinc dienolates
-
Copper-catalyzed conjugate addition of organozinc reagents to reactive allenic esters providing zinc dienolates: Oisaki, K., Zhao, D., Kanai, M., and Shibasaki, M. J. Am. Chem. Soc. 2007, 129, 7439
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 7439
-
-
Oisaki, K.1
Zhao, D.2
Kanai, M.3
Shibasaki, M.4
-
33
-
-
0345887400
-
-
Addition to allenes bearing a directing hydroxy group providing allylzincs
-
Addition to allenes bearing a directing hydroxy group providing allylzincs: Richey, H. G., Jr. and Szucs, S. S. Tetrahedron Lett. 1971, 41, 3785
-
(1971)
Tetrahedron Lett.
, vol.41
, pp. 3785
-
-
Richey Jr., H.G.1
Szucs, S.S.2
-
34
-
-
33845799176
-
-
Efficient three-component coupling of allenes, Grignard reagents, and chlorosilanes or alkyl halides was reported. However, precise mechanistic investigations of the reactions showed that generation of allylmagnesium intermediates might not be a major pathway
-
Efficient three-component coupling of allenes, Grignard reagents, and chlorosilanes or alkyl halides was reported. However, precise mechanistic investigations of the reactions showed that generation of allylmagnesium intermediates might not be a major pathway: Fujii, Y., Terao, J., Kuniyasu, H., and Kambe, N. J. Organomet. Chem. 2007, 692, 375
-
(2007)
J. Organomet. Chem.
, vol.692
, pp. 375
-
-
Fujii, Y.1
Terao, J.2
Kuniyasu, H.3
Kambe, N.4
-
35
-
-
33748805474
-
-
Krasovskiy, A., Malakhov, V., Gavryushin, A., and Knochel, P. Angew. Chem., Int. Ed. 2006, 45, 6040
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6040
-
-
Krasovskiy, A.1
Malakhov, V.2
Gavryushin, A.3
Knochel, P.4
-
36
-
-
46149094730
-
-
Metzger, A., Schade, M. A., and Knochel, P. Org. Lett. 2008, 10, 1107
-
(2008)
Org. Lett.
, vol.10
, pp. 1107
-
-
Metzger, A.1
Schade, M.A.2
Knochel, P.3
-
37
-
-
0036847530
-
-
The regioselectivity of the allylic substitution reaction with allylic copper reagents is known to heavily depend on substrates and reagents used. See
-
The regioselectivity of the allylic substitution reaction with allylic copper reagents is known to heavily depend on substrates and reagents used. See: Liepins, V. and Bäckvall, J.-E. Eur. J. Org. Chem. 2002, 3527
-
(2002)
Eur. J. Org. Chem.
, pp. 3527
-
-
Liepins, V.1
Bäckvall, J.-E.2
-
38
-
-
0028233573
-
-
Yanagisawa, A., Nomura, N., and Yamamoto, H. Tetrahedron 1994, 50, 6017
-
(1994)
Tetrahedron
, vol.50
, pp. 6017
-
-
Yanagisawa, A.1
Nomura, N.2
Yamamoto, H.3
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