-
4
-
-
0000840554
-
-
F. Bohlmann, C. Scheidges, C. Zdero, R.M. King, and H. Robinson Phytochemistry 23 1984 1109
-
(1984)
Phytochemistry
, vol.23
, pp. 1109
-
-
Bohlmann, F.1
Scheidges, C.2
Zdero, C.3
King, R.M.4
Robinson, H.5
-
5
-
-
0026622946
-
-
C.K. Lau, P.C. Belanger, C. Dufresne, J. Scheigetz, M. Therien, B. Fitzsimmons, R.N. Young, A.W. Ford-Hutchinson, D. Riendeau, D. Denis, J. Guay, C. Charleson, H. Piechuta, C.S. McFarlane, S.H. Lee Chiu, D. Eline, R.F. Alvaro, G. Miwa, and J.L. Walsh J. Med. Chem. 35 1992 1299
-
(1992)
J. Med. Chem.
, vol.35
, pp. 1299
-
-
Lau, C.K.1
Belanger, P.C.2
Dufresne, C.3
Scheigetz, J.4
Therien, M.5
Fitzsimmons, B.6
Young, R.N.7
Ford-Hutchinson, A.W.8
Riendeau, D.9
Denis, D.10
Guay, J.11
Charleson, C.12
Piechuta, H.13
McFarlane, C.S.14
Lee Chiu, S.H.15
Eline, D.16
Alvaro, R.F.17
Miwa, G.18
Walsh, J.L.19
-
6
-
-
0032908552
-
-
M.R. Hellberg, A. Namil, P. Delgado, K.C. David, T.L. Kessler, G. Graff, K.S. Haggard, and J.C. Nixon J. Med. Chem. 42 1999 267
-
(1999)
J. Med. Chem.
, vol.42
, pp. 267
-
-
Hellberg, M.R.1
Namil, A.2
Delgado, P.3
David, K.C.4
Kessler, T.L.5
Graff, G.6
Haggard, K.S.7
Nixon, J.C.8
-
7
-
-
21344447280
-
-
W. Pfefferle, H. Anke, M. Bross, B. Steffan, R. Vianden, and W. Steglich J. Antibiot. 43 1990 649
-
(1990)
J. Antibiot.
, vol.43
, pp. 649
-
-
Pfefferle, W.1
Anke, H.2
Bross, M.3
Steffan, B.4
Vianden, R.5
Steglich, W.6
-
11
-
-
0000559013
-
-
W.A. Bonner, N.I. Burke, W.E. Fleck, R.K. Hill, J.A. Joule, B. Sjoberg, and J.H. Zalkow Tetrahedron 20 1964 1419
-
(1964)
Tetrahedron
, vol.20
, pp. 1419
-
-
Bonner, W.A.1
Burke, N.I.2
Fleck, W.E.3
Hill, R.K.4
Joule, J.A.5
Sjoberg, B.6
Zalkow, J.H.7
-
12
-
-
0032544954
-
-
T. Saito, T. Suzuki, M. Morimoto, C. Akiyama, T. Ochiai, K. Takeuchi, T. Matsumoto, and K. Suzuki J. Am. Chem. Soc. 120 1998 11633
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 11633
-
-
Saito, T.1
Suzuki, T.2
Morimoto, M.3
Akiyama, C.4
Ochiai, T.5
Takeuchi, K.6
Matsumoto, T.7
Suzuki, K.8
-
13
-
-
0000222470
-
-
W.N. White, D. Gwynn, R. Schlitt, C. Girard, and W. Fife J. Am. Chem. Soc. 80 1958 3271
-
(1958)
J. Am. Chem. Soc.
, vol.80
, pp. 3271
-
-
White, W.N.1
Gwynn, D.2
Schlitt, R.3
Girard, C.4
Fife, W.5
-
16
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21344468847
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note
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+, 100%).
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20
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21344443461
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note
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3 in a mixture of reagent grade acetone and distilled water at 0°C. Here, Oxone serves as a stoichiometric oxidizing agent under a variety of conditions. Therefore, an aqueous solution of Oxone can be used to perform oxidations in homogeneous solution and in biphasic systems using an immiscible co-solvent and a phase transfer catalyst at pH 7 to prevent hydrolysis of the epoxide.
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22
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21344469088
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note
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+, 285, 100%).
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23
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0031024261
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E.N. Jacobsen, F. Kakiuchi, R.G. Konsler, J.F. Larrow, and M. Tokunaga Tetrahedron Lett. 38 1997 773
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 773
-
-
Jacobsen, E.N.1
Kakiuchi, F.2
Konsler, R.G.3
Larrow, J.F.4
Tokunaga, M.5
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25
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21344467471
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note
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iPrOH/n-hexane, flow rate: 1 mL/min, ee: 80%}.
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26
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21344448841
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Unpublished results, Indian Institute of Chemical Technology, Hyderabad, India
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Rao, B. V.; Sitharamaiah, D. Unpublished results, Indian Institute of Chemical Technology, Hyderabad, India, 1998.
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(1998)
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Rao, B.V.1
Sitharamaiah, D.2
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27
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21344466089
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note
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iPrOH/n-hexane, flow rate: 1 mL/min, ee: 75%}.
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