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(a) Shell Oil, Eng. Patent 1, 249, 079, 1971; Chem. Abstr. 74 (1971) 12981m.
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6
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(f) I.W.C.W. Arends, R.A. Sheldon, M. Wallau, U. Schuchardt, Angew. Chem. 109 (1997) 1190; Angew. Chem. Int. Ed. Engl. 36 (1997) 1144.
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Arends, I.W.C.W.1
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7
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0030852830
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(f) I.W.C.W. Arends, R.A. Sheldon, M. Wallau, U. Schuchardt, Angew. Chem. 109 (1997) 1190; Angew. Chem. Int. Ed. Engl. 36 (1997) 1144.
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9
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84941216140
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J.D. Morrison (Ed.), Aademic Press, New York
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(b) M.G. Finn, K.B. Sharpless, in: J.D. Morrison (Ed.), Asymmetric Synthesis, Vol. 5, Aademic Press, New York, 1986, p. 247.
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Asymmetric Synthesis
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Finn, M.G.1
Sharpless, K.B.2
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12
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0000655043
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(b) C. Girard, H.B. Kagan, Angew. Chem. 110 (1998) 3088; Angew. Chem. Int. Ed. Engl. 37 (1998) 2922; this review article summarizes the publications of H.B. Kagan on this topic. For further reactions of this type
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Angew. Chem.
, vol.110
, pp. 3088
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Girard, C.1
Kagan, H.B.2
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13
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0032538773
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(b) C. Girard, H.B. Kagan, Angew. Chem. 110 (1998) 3088; Angew. Chem. Int. Ed. Engl. 37 (1998) 2922; this review article summarizes the publications of H.B. Kagan on this topic. For further reactions of this type
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(1998)
Angew. Chem. Int. Ed. Engl.
, vol.37
, pp. 2922
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-
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14
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0030807222
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cit. lit
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© M. Bouchio, S. Calloni, F. Di Furia, G. Licini, G. Modena, S. Moro, W.A. Nugent, J. Am. Chem. Soc. 119 (1997) 6935 cit. lit.
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J. Am. Chem. Soc.
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Bouchio, M.1
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15
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33751386816
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(d) N. Komatsu, M. Hashizume, T. Sugia, S. Uemura, J. Org. Chem. 58 (1993) 4529.
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Komatsu, N.1
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16
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0028942240
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M. Schulz, R. Kluge, M. Schüler, G. Hoffmann, Tetrahedron 51 (1995) 3175.
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(1995)
Tetrahedron
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Schulz, M.1
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Hoffmann, G.4
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19
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0003031180
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G. Hollingworth, earlier lit. cit
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(a) M. Julia, V. Pfeuty-Saint-Jalmes, K. Ple, J.-N. Verpeaux, in part G. Hollingworth, Bull. Soc. Chim. Fr. 133 (1996) 15, earlier lit. cit.
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Bull. Soc. Chim. Fr.
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Julia, M.1
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33748240609
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(b) G. Boche, F. Bosold, J.C.W. Lohrenz, Angew. Chem. 106 (1994) 1228; Angew. Chem. Int. Ed. Engl. 33 (1994) 1161.
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Angew. Chem. Int. Ed. Engl.
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24
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33947337524
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(e) G.M. Whitesides, J. San Filippo, J.P. Casey, E.J. Panek, J. Am. Chem. Soc. 89 (1967) 5302.
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Whitesides, G.M.1
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Panek, E.J.4
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25
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0011624445
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(f) H. Neumann, D. Seebach, Chem. Ber. 111 (1978) 2782 also used oxenoids LiOOR to oxidize vinyllithium compounds.
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(1978)
Chem. Ber.
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Neumann, H.1
Seebach, D.2
-
26
-
-
84992264935
-
-
note
-
3 (or a dimer, thereof) and isopropanol [2] which is also acidic. Apparently the reaction of the organometallic species RM with the titanium peroxide [8] is much faster than the protonation of RM by the available proton sources. Similar behaviour of RLi in other competition reactions is known [9].
-
-
-
-
27
-
-
0029960797
-
-
Solid state structure and oxidation reactions of a Ti-peroxide: G. Boche, K. Möbus, K. Harms, M. Marsch, J. Am. Chem. Soc. 118 (1996) 2770.
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J. Am. Chem. Soc.
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Boche, G.1
Möbus, K.2
Harms, K.3
Marsch, M.4
-
28
-
-
0001420491
-
-
Other reactions of RLi in the presence of acidic protons: (a) H.W. Whitlock, B.J. Whitlock, R.J. Boatman, J. Am. Chem. Soc. 99 (1977) 4822. (b) P. Beak, T.J. Musick, C.-W. Chen, J. Am. Chem. 110 (1988) 3538. © W.F. Bailey, J.J. Patricia, T.T. Nurmi, W. Wang, Tetrahedron Lett. 27 (1986) 1861. (d) N.S. Narasimhan, N.M. Sunder, R. Ammanamanchi, B.D. Bonde, J. Am. Chem. Soc. 112 (1990) 4931. (e) A. Schmidt, G. Köbrich, R.W. Hoffmann, Chem. Ber. 124 (1991) 1253.
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J. Am. Chem. Soc.
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Whitlock, H.W.1
Whitlock, B.J.2
Boatman, R.J.3
-
29
-
-
0346541368
-
-
Other reactions of RLi in the presence of acidic protons: (a) H.W. Whitlock, B.J. Whitlock, R.J. Boatman, J. Am. Chem. Soc. 99 (1977) 4822. (b) P. Beak, T.J. Musick, C.-W. Chen, J. Am. Chem. 110 (1988) 3538. © W.F. Bailey, J.J. Patricia, T.T. Nurmi, W. Wang, Tetrahedron Lett. 27 (1986) 1861. (d) N.S. Narasimhan, N.M. Sunder, R. Ammanamanchi, B.D. Bonde, J. Am. Chem. Soc. 112 (1990) 4931. (e) A. Schmidt, G. Köbrich, R.W. Hoffmann, Chem. Ber. 124 (1991) 1253.
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J. Am. Chem.
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, pp. 3538
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Beak, P.1
Musick, T.J.2
Chen, C.-W.3
-
30
-
-
0000754130
-
-
Other reactions of RLi in the presence of acidic protons: (a) H.W. Whitlock, B.J. Whitlock, R.J. Boatman, J. Am. Chem. Soc. 99 (1977) 4822. (b) P. Beak, T.J. Musick, C.-W. Chen, J. Am. Chem. 110 (1988) 3538. © W.F. Bailey, J.J. Patricia, T.T. Nurmi, W. Wang, Tetrahedron Lett. 27 (1986) 1861. (d) N.S. Narasimhan, N.M. Sunder, R. Ammanamanchi, B.D. Bonde, J. Am. Chem. Soc. 112 (1990) 4931. (e) A. Schmidt, G. Köbrich, R.W. Hoffmann, Chem. Ber. 124 (1991) 1253.
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(1986)
Tetrahedron Lett.
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, pp. 1861
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Bailey, W.F.1
Patricia, J.J.2
Nurmi, T.T.3
Wang, W.4
-
31
-
-
0000006651
-
-
Other reactions of RLi in the presence of acidic protons: (a) H.W. Whitlock, B.J. Whitlock, R.J. Boatman, J. Am. Chem. Soc. 99 (1977) 4822. (b) P. Beak, T.J. Musick, C.-W. Chen, J. Am. Chem. 110 (1988) 3538. © W.F. Bailey, J.J. Patricia, T.T. Nurmi, W. Wang, Tetrahedron Lett. 27 (1986) 1861. (d) N.S. Narasimhan, N.M. Sunder, R. Ammanamanchi, B.D. Bonde, J. Am. Chem. Soc. 112 (1990) 4931. (e) A. Schmidt, G. Köbrich, R.W. Hoffmann, Chem. Ber. 124 (1991) 1253.
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J. Am. Chem. Soc.
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Narasimhan, N.S.1
Sunder, N.M.2
Ammanamanchi, R.3
Bonde, B.D.4
-
32
-
-
0001380231
-
-
Other reactions of RLi in the presence of acidic protons: (a) H.W. Whitlock, B.J. Whitlock, R.J. Boatman, J. Am. Chem. Soc. 99 (1977) 4822. (b) P. Beak, T.J. Musick, C.-W. Chen, J. Am. Chem. 110 (1988) 3538. © W.F. Bailey, J.J. Patricia, T.T. Nurmi, W. Wang, Tetrahedron Lett. 27 (1986) 1861. (d) N.S. Narasimhan, N.M. Sunder, R. Ammanamanchi, B.D. Bonde, J. Am. Chem. Soc. 112 (1990) 4931. (e) A. Schmidt, G. Köbrich, R.W. Hoffmann, Chem. Ber. 124 (1991) 1253.
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(1991)
Chem. Ber.
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Schmidt, A.1
Köbrich, G.2
Hoffmann, R.W.3
-
33
-
-
0011555501
-
-
See Ref. [11]
-
tButylperoxy-1,3,2-dioxaborolan was used for such oxidations by: R.W. Hoffmann, K. Dittrich, Synthesis (1983) 107. See Ref. [11].
-
(1983)
Synthesis
, pp. 107
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-
Hoffmann, R.W.1
Dittrich, K.2
-
37
-
-
84992240244
-
-
note
-
2MgBr from benzyl bromide and magnesium.
-
-
-
-
38
-
-
0028959933
-
-
Oxidation of Zn compounds: (a) P. Knochel, I. Klement, H. Lütjens, Tetrahedron Lett. 36 (1995) 3161. (b) I. Klement, P. Knochel, Synlett (1995) 1113.
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(1995)
Tetrahedron Lett.
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, pp. 3161
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-
Knochel, P.1
Klement, I.2
Lütjens, H.3
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39
-
-
85064868698
-
-
Oxidation of Zn compounds: (a) P. Knochel, I. Klement, H. Lütjens, Tetrahedron Lett. 36 (1995) 3161. (b) I. Klement, P. Knochel, Synlett (1995) 1113.
-
(1995)
Synlett
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-
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Klement, I.1
Knochel, P.2
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40
-
-
33947337524
-
-
(a) G.M. Whitesides, J. San Filippo, J.P. Casey, E.J. Panek, J. Am. Chem. Soc. 89 (1967) 5302.
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(1967)
J. Am. Chem. Soc.
, vol.89
, pp. 5302
-
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Whitesides, G.M.1
San Filippo, J.2
Casey, J.P.3
Panek, E.J.4
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41
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0346471289
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-
(b) B.H. Lipshutz, K. Siegmann, E. Garcia, F. Kayser, J. Am. Chem. Soc. 115 (1993) 9276.
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Lipshutz, B.H.1
Siegmann, K.2
Garcia, E.3
Kayser, F.4
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42
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0000439467
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G. Boche, K. Möbus, K. Harms, J.C.W. Lohrenz, M. Marsch, Chem. Eur. J. 2 (1996) 604.
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(1996)
Chem. Eur. J.
, vol.2
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Boche, G.1
Möbus, K.2
Harms, K.3
Lohrenz, J.C.W.4
Marsch, M.5
-
43
-
-
84992244108
-
-
Ph.D. Thesis, in progress, R.W. Hoffmann, personal communication, Marburg
-
This was also observed by: Bettina Hölzer, Ph.D. Thesis, in progress, R.W. Hoffmann, personal communication, Marburg, 2000.
-
(2000)
-
-
Hölzer, B.1
-
44
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84992263221
-
-
Dissertation, Universität München
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(a) D. Schneider, Dissertation, Universität München, 1977.
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(1977)
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Schneider, D.1
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46
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0000030233
-
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© C.L. Osborn, T.C. Shields, B.A. Shoulders, J.F. Krause, H.V. Cortez, P.D. Gardner, J. Am. Chem. Soc. 87 (1965) 3158.
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J. Am. Chem. Soc.
, vol.87
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Osborn, C.L.1
Shields, T.C.2
Shoulders, B.A.3
Krause, J.F.4
Cortez, H.V.5
Gardner, P.D.6
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49
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0010918143
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(f) T. Hirao, T. Hasegawa, Y. Ohshiro, I. Ikeda, J. Org. Chem. 58 (1993) 6529.
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J. Org. Chem.
, vol.58
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Hirao, T.1
Hasegawa, T.2
Ohshiro, Y.3
Ikeda, I.4
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50
-
-
0343258500
-
-
E.A. Dehmlow, Angew. Chem. 89 (1977) 521; Angew. Chem. Int. Ed. Engl. 16 (1977) 493.
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(1977)
Angew. Chem.
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, pp. 521
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Dehmlow, E.A.1
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51
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84980186036
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E.A. Dehmlow, Angew. Chem. 89 (1977) 521; Angew. Chem. Int. Ed. Engl. 16 (1977) 493.
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(1977)
Angew. Chem. Int. Ed. Engl.
, vol.16
, pp. 493
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-
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52
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0345910252
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Stereochemistry: N.I. Yakushkina, G.A. Zakharova, L.S. Surmina, I.G. Bolesov, J. Org. Chem. USSR 19 (1980) 1553.
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(1980)
J. Org. Chem. USSR
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Yakushkina, N.I.1
Zakharova, G.A.2
Surmina, L.S.3
Bolesov, I.G.4
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53
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0003471628
-
-
S. Patai, Z. Rappoport (Eds.), Wiley, New York
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The stereoselective preparation, configurational stability and stereochemistry of the reaction of cyclopropyllithium and cyclopropyl Grignard compounds with electrophiles is discussed in detail in: G. Boche, H.M. Walborsky, in: S. Patai, Z. Rappoport (Eds.), Cyclopropane Derived Reactive Intermediates, Wiley, New York, 1990.
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(1990)
Cyclopropane Derived Reactive Intermediates
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Boche, G.1
Walborsky, H.M.2
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54
-
-
0000343373
-
-
The stereoselective formation, configurational stability and reaction with electrophiles with retention of configuration of cyclopropyl cuprates has been studied by: (a) K. Kitatani, T. Hiyama, H. Nozaki, Bull. Chem. Soc. Jpn 1977, 50, 1600.
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(1977)
Bull. Chem. Soc. Jpn
, vol.50
, pp. 1600
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Kitatani, K.1
Hiyama, T.2
Nozaki, H.3
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55
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33847089969
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(b) H. Yamamoto, K. Kitatami, T. Hiyama, H. Nozaki, J. Am. Chem. Soc. 1977, 99, 5816.
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J. Am. Chem. Soc.
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Yamamoto, H.1
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Hiyama, T.3
Nozaki, H.4
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57
-
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84992249280
-
-
-1) after the extraction workup procedure. The yields were determined by calculation from calibration plots
-
-1) after the extraction workup procedure. The yields were determined by calculation from calibration plots.
-
-
-
|