-
2
-
-
0000343373
-
-
For pioneering studies on cuprates, see: 1977 J. Am. Chem. Soc. 1976 98 2362 J. Am. Chem. Soc. 1967 89 3911 Tetrahedron Lett. 1970 11 315 Tetrahedron Lett. 1972 13 293 Synthesis 1993 1063
-
For pioneering studies on cuprates, see:, Kitatani K, Hiyama T, Nozaki H, Bull. Chem. Soc. Jpn. 1977 50 1600, Kitatani K, Hiyama T, Nozaki H, J. Am. Chem. Soc. 1976 98 2362, Corey E J., Posner G H., J. Am. Chem. Soc. 1967 89 3911, Corey E J., Posner G H., Tetrahedron Lett. 1970 11 315, Posner G H., Brunelle D J., Tetrahedron Lett. 1972 13 293, Martínez A G., Fernández A H., Alvarez R M., Barcina J O., Gómez C G., Subramanian L R., Synthesis 1993 1063
-
Bull. Chem. Soc. Jpn.
, vol.50
, pp. 1600
-
-
Kitatani, K.1
Hiyama, T.2
Nozaki, H.3
Kitatani, K.4
Hiyama, T.5
Nozaki, H.6
Corey, E.J.7
Posner, G.H.8
Corey, E.J.9
Posner, G.H.10
Posner, G.H.11
Brunelle, D.J.12
Martínez, A.G.13
Fernández, A.H.14
Alvarez, R.M.15
Barcina, J.O.16
Gómez, C.G.17
Subramanian, L.R.18
-
3
-
-
0026073043
-
-
For selected recent reactions with other organometallic reagents, see: 1991 Synlett 2001 818 Bull. Chem. Soc. Jpn. 2000 73 2139 Chem. Eur. J. 2002 8 1730 Tetrahedron 2002 58 1581 Angew. Chem. Int. Ed. 2000 39 1462
-
For selected recent reactions with other organometallic reagents, see:, Harada T, Kotani Y, Katsuhira T, Oku A, Tetrahedron Lett. 1991 32 1573, Shibli A, Varghese J P., Marek I, Synlett 2001 818, Kakiya H, Shinokubo H, Oshima K, Bull. Chem. Soc. Jpn. 2000 73 2139, Inoue A, Kondo J, Shinokubo H, Oshima K, Chem. Eur. J. 2002 8 1730, Baird M S., Nizovtsev [nl]A V., Bolesov I G., Tetrahedron 2002 58 1581, Hoffmann R W., Knopff O, Kusche A, Angew. Chem. Int. Ed. 2000 39 1462
-
Tetrahedron Lett.
, vol.32
, pp. 1573
-
-
Harada, T.1
Kotani, Y.2
Katsuhira, T.3
Oku, A.4
Shibli, A.5
Varghese, J.P.6
Marek, I.7
Kakiya, H.8
Shinokubo, H.9
Oshima, K.10
Inoue, A.11
Kondo, J.12
Shinokubo, H.13
Oshima, K.14
Baird, M.S.15
Nizovtsev, A.V.16
Bolesov, I.G.17
Hoffmann, R.W.18
Knopff, O.19
Kusche, A.20
more..
-
4
-
-
53149143210
-
-
2008 Tetrahedron Lett. 2009 50 3270
-
Someya H, Ohmiya H, Yorimitsu H, Oshima K, Org. Lett. 2008 10 969, Someya H, Yorimitsu H, Oshima K, Tetrahedron Lett. 2009 50 3270
-
Org. Lett.
, vol.10
, pp. 969
-
-
Someya, H.1
Ohmiya, H.2
Yorimitsu, H.3
Oshima, K.4
Someya, H.5
Yorimitsu, H.6
Oshima, K.7
-
5
-
-
0036643488
-
-
2), see: 2002 Synthesis 1971 303
-
2), see:, Kochi J K., J. Organomet. Chem. 2002 653 11, Tamura M, Kochi J K., Synthesis 1971 303
-
J. Organomet. Chem.
, vol.653
, pp. 11
-
-
Kochi, J.K.1
Tamura, M.2
Kochi, J.K.3
-
6
-
-
26844579215
-
-
Silver-catalyzed oxidative homocoupling reactions of Grignard reagents have been reported, see: 2005 Bull. Chem. Soc. Jpn. 1972 45 1120
-
Silver-catalyzed oxidative homocoupling reactions of Grignard reagents have been reported, see:, Nagano T, Hayashi T, Chem. Lett. 2005 34 1152, Tamura M, Kochi J K., Bull. Chem. Soc. Jpn. 1972 45 1120
-
Chem. Lett.
, vol.34
, pp. 1152
-
-
Nagano, T.1
Hayashi, T.2
Tamura, M.3
Kochi, J.K.4
-
7
-
-
74549148328
-
-
note
-
22: C, 89.65; H, 10.35. Found: C, 89.51; H, 10.07
-
-
-
-
8
-
-
74549114213
-
-
Organoargentate complexes are rarely reported, see: Wiley New York 1999 Chap. 7 In Comprehensive Organometallic Chemistry II Pergamon Oxford 1995 Chap. 2 Organometallics 2009 28; and references cited therein J. Am. Chem. Soc. 2005 127 1446; and references cited therein J. Organomet. Chem. 1999 589 234
-
Organoargentate complexes are rarely reported, see:, Schmidbaur H, Bayler A, The Chemistry of Organic Derivatives of Gold and Silver, Patai S, Rappoport Z, Wiley New York 1999 Chap. 7, Noltes J G., van Koten G, In Comprehensive Organometallic Chemistry II Vol. 3, Wardell J L., Pergamon Oxford 1995 Chap. 2, Rijs N J., OHair R A. J., Organometallics 2009 28 2684; and references cited therein, Nakanishi W, Yamanaka M, Nakamura E, J. Am. Chem. Soc. 2005 127 1446; and references cited therein, Hwang C.-S, Power P P., J. Organomet. Chem. 1999 589 234
-
The Chemistry of Organic Derivatives of Gold and Silver
, vol.3
, pp. 2684
-
-
Schmidbaur, H.1
Bayler, A.2
Patai, S.3
Rappoport, Z.4
Noltes, J.G.5
Van Koten, G.6
Wardell, J.L.7
Rijs, N.J.8
Ohair, R.A.J.9
Nakanishi, W.10
Yamanaka, M.11
Nakamura, E.12
Hwang, C.-S.13
Power, P.P.14
-
9
-
-
0000534688
-
-
Triethylaluminum is known to react with,-dichloro-toluene to yield 3-phenylpentane via a carbocation intermediate, see: 1966
-
Triethylaluminum is known to react with,-dichloro-toluene to yield 3-phenylpentane via a carbocation intermediate, see:, Miller D B., J. Org. Chem. 1966 31 908
-
J. Org. Chem.
, vol.31
, pp. 908
-
-
Miller, D.B.1
-
10
-
-
74549174672
-
-
1996 In Organic Synthesis: Theory and Applications Vol. 2 JAI Press Greenwich CT 1993 27-66
-
Wender P A., Chem. Rev. 1996 96 1, Wender [nl]P A., Miller B L., In Organic Synthesis: Theory and Applications Vol. 2, Hudlicky T, JAI Press Greenwich CT 1993 27-66
-
Chem. Rev.
, vol.96
, pp. 1
-
-
Wender, P.A.1
Wender, P.A.2
Miller, B.L.3
Hudlicky, T.4
-
11
-
-
1542763298
-
-
1995 J. Chem. Soc., Perkin Trans. 1 1998 371
-
Grubbs R H., Miller S J., Fu G C., Acc. Chem. Res. 1995 28 446, Armstrong S K., J. Chem. Soc., Perkin Trans. 1 1998 371
-
Acc. Chem. Res.
, vol.28
, pp. 446
-
-
Grubbs, R.H.1
Miller, S.J.2
Fu, G.C.3
Armstrong, S.K.4
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