-
5
-
-
0032557705
-
-
Demir A.S., Hamamci H., Tanyeli C., Akhmedov I.M., Doganel F. Tetrahedron: Asymmetry. 9:1998;1673.
-
(1998)
Tetrahedron: Asymmetry
, vol.9
, pp. 1673
-
-
Demir, A.S.1
Hamamci, H.2
Tanyeli, C.3
Akhmedov, I.M.4
Doganel, F.5
-
6
-
-
0000325583
-
-
Demir A.S., Camkerten N., Akgun H., Tanyeli C., Mahasneh A.S., Watt D.S. Synth. Commun. 20:1990;2279.
-
(1990)
Synth. Commun.
, vol.20
, pp. 2279
-
-
Demir, A.S.1
Camkerten, N.2
Akgun, H.3
Tanyeli, C.4
Mahasneh, A.S.5
Watt, D.S.6
-
10
-
-
33947329731
-
-
3 together with the rate of the reaction. However, yields were relatively unaffected:
-
3 together with the rate of the reaction. However, yields were relatively unaffected: Bush J.B. Jr., Finkbeiner H. J. Am. Chem. Soc. 90:1968;5903.
-
(1968)
J. Am. Chem. Soc.
, vol.90
, pp. 5903
-
-
Bush Jr., J.B.1
Finkbeiner, H.2
-
15
-
-
84980126475
-
-
Mihailovic M.L., Forsek J., Lorenc L., Maksiomovic Z., Fuhrer H., Kalvoda J. Helv. Chim. Acta. 52:1969;459.
-
(1969)
Helv. Chim. Acta
, vol.52
, pp. 459
-
-
Mihailovic, M.L.1
Forsek, J.2
Lorenc, L.3
Maksiomovic, Z.4
Fuhrer, H.5
Kalvoda, J.6
-
16
-
-
0033597429
-
-
4 mediated acetoxylation of steroidal substrates has been reported; for recent examples see: (b)
-
4 mediated acetoxylation of steroidal substrates has been reported; for recent examples see: (b) Ferreira M.R.C., Hernando J.I.M., Lena J.I.C., Moral J.Q., Arseniyadis S. Tetrahedron: Asymmetry. 10:1999;1527.
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 1527
-
-
Ferreira, M.R.C.1
Hernando, J.I.M.2
Lena, J.I.C.3
Moral, J.Q.4
Arseniyadis, S.5
-
17
-
-
0001659471
-
-
Hernando J.I.M., Ferreira M.R.C., Lena J.I.C., Toupet L., Birlirakis N., Arseniyadis S. Tetrahedron: Asymmetry. 10:1999;3977.
-
(1999)
Tetrahedron: Asymmetry
, vol.10
, pp. 3977
-
-
Hernando, J.I.M.1
Ferreira, M.R.C.2
Lena, J.I.C.3
Toupet, L.4
Birlirakis, N.5
Arseniyadis, S.6
-
23
-
-
0242391636
-
-
3 oxidation of saturated ketones provide complex mixtures:
-
3 oxidation of saturated ketones provide complex mixtures: Okano M., Aratani T. Bull. Chem. Soc. Jpn. 49:1976;2811.
-
(1976)
Bull. Chem. Soc. Jpn.
, vol.49
, pp. 2811
-
-
Okano, M.1
Aratani, T.2
-
24
-
-
0029869740
-
-
Snider stated that oxidation of α′-keto radical derived from enones is a very fast process relative to oxidation of radicals derived from saturated ketones. Attempted alkene addition to an enone in the presence of 1-octene provided only acetoxylation and oligomer: (a)
-
Snider stated that oxidation of α′-keto radical derived from enones is a very fast process relative to oxidation of radicals derived from saturated ketones. Attempted alkene addition to an enone in the presence of 1-octene provided only acetoxylation and oligomer: (a) Snider B.B., Kiselgof E.Y. Tetrahedron. 52:1996;6073.
-
(1996)
Tetrahedron
, vol.52
, pp. 6073
-
-
Snider, B.B.1
Kiselgof, E.Y.2
-
25
-
-
0030858681
-
-
Successful intermolecular addition of enones to alkenes providing dihydrobenzofurans was reported: (b)
-
Successful intermolecular addition of enones to alkenes providing dihydrobenzofurans was reported: (b) Snider B.B., Han L., Xie C. J. Org. Chem. 62:1997;6978.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6978
-
-
Snider, B.B.1
Han, L.2
Xie, C.3
-
26
-
-
0345731482
-
-
3 to mediate reactions that is possibly based on reductive elimination of arylmanganese intermediates:
-
3 to mediate reactions that is possibly based on reductive elimination of arylmanganese intermediates: Demir A.S., Reis Ö., Emrullahoglu M. J. Org. Chem. 68:2003;10130.
-
(2003)
J. Org. Chem.
, vol.68
, pp. 10130
-
-
Demir, A.S.1
Reis, Ö.2
Emrullahoglu, M.3
-
27
-
-
0001556501
-
-
Curran D.P., Morgan T.M., Schwartz C.E., Snider B.B., Dombroski M.A. J. Am. Chem. Soc. 113:1991;6607.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 6607
-
-
Curran, D.P.1
Morgan, T.M.2
Schwartz, C.E.3
Snider, B.B.4
Dombroski, M.A.5
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