-
2
-
-
0003579939
-
-
L. A. Paquette, John Wiley and Sons, New York, 1995; vol. 7, p. 4728
-
(b) Encyclopedia of Reagents for Organic Synthesis, éd. L. A. Paquette, John Wiley and Sons, New York, 1995; vol. 7, p. 4728;
-
Encyclopedia of Reagents for Organic Synthesis, Éd.
-
-
-
3
-
-
0043162088
-
-
M. Sato, Y. Morizawa, K. Oshima and H. Nozaki
-
H. Oda, M. Sato, Y. Morizawa, K. Oshima and H. Nozaki, Tetrahedron, 1985, 41, 3257.
-
Tetrahedron, 1985, 41, 3257.
-
-
Oda, H.1
-
5
-
-
0001259709
-
-
S. Miyata, M. Nakatsuka and T. Saegusa
-
(b) Y. Ito, S. Miyata, M. Nakatsuka and T. Saegusa, J. Org. Chem., 1981, 46, 1043;
-
J. Org. Chem., 1981, 46, 1043
-
-
Ito, Y.1
-
7
-
-
84987240379
-
-
M. J. Begley, P. Cornwall and D. W. Knight
-
S. B. Bedford, M. J. Begley, P. Cornwall and D. W. Knight, Synlett, 1991, 627.
-
Synlett, 1991, 627.
-
-
Bedford, S.B.1
-
9
-
-
2942617947
-
-
(b) R. K. Sachs and S. R. Kass, J. Am. Chem. Soc, , 1994, 116, 783;
-
J. Am. Chem. Soc, , 1994, 116, 783
-
-
Sachs, R.K.1
Kass, S.R.2
-
11
-
-
0001013904
-
-
S. Gronert, S. E. Barlow, V. M. Bierbaum and R. Damrauer.a
-
C. H. DePuy, S. Gronert, S. E. Barlow, V. M. Bierbaum and R. Damrauer.a Am. Chem. Soc., 1989, 111, 1968.
-
Am. Chem. Soc., 1989, 111, 1968.
-
-
Depuy, C.H.1
-
13
-
-
33746404034
-
-
PhD Thesis, University of Minnesota, 1997.
-
S. Han, PhD Thesis, University of Minnesota, 1997.
-
-
-
-
15
-
-
0027969099
-
-
N. Akihiro, Y. Makioka, K. Takaki and Y. Fujiwara
-
(b) Y. Taniguchi, N. Akihiro, Y. Makioka, K. Takaki and Y. Fujiwara, Tetrahedron Lett., 1994, 35, 6897;
-
Tetrahedron Lett., 1994, 35, 6897
-
-
Taniguchi, Y.1
-
16
-
-
0000057018
-
-
R. Calas, J. Donogues, N. Duffaut, J. Gerval and P. Lapouyade
-
J. P. Picard, R. Calas, J. Donogues, N. Duffaut, J. Gerval and P. Lapouyade, J. Org. Chem., 1979, 44, 420;
-
J. Org. Chem., 1979, 44, 420
-
-
Picard, J.P.1
-
18
-
-
0000856284
-
-
A. Hayashi, S. Suzuki and J. Tsug
-
(e) K. Yamamoto, A. Hayashi, S. Suzuki and J. Tsug, Organometallics., 1987, 6, 974.
-
Organometallics., 1987, 6, 974.
-
-
Yamamoto, K.1
-
19
-
-
33947335842
-
-
J. M. Duff, P. R Jones and N. R. Davis
-
(a) A. G. Brook, J. M. Duff, P. R Jones and N. R. Davis, J. Am. Chem. Soc., 1967, 89, 431;
-
J. Am. Chem. Soc., 1967, 89, 431
-
-
Brook, A.G.1
-
23
-
-
33746435611
-
-
3 or KOH in alcohol solvents.
-
3 or KOH in alcohol solvents.
-
-
-
-
24
-
-
0040981211
-
-
ed. P. De Mayo, John Wiley and Sons, New York, 1963, vol. 1, p. 257
-
(a) Molecular Rearrangements, ed. P. De Mayo, John Wiley and Sons, New York, 1963, vol. 1, p. 257;
-
Molecular Rearrangements
-
-
-
29
-
-
0003408677
-
-
eds. C. H. Bamford and C. F. H. Tipper, Elsevier, New York, 1973, vol. 9, p. 470
-
R. H. DeWolfe, Comprehensive Chemical Kinetics, eds. C. H. Bamford and C. F. H. Tipper, Elsevier, New York, 1973, vol. 9, p. 470;
-
Comprehensive Chemical Kinetics
-
-
Dewolfe, R.H.1
-
32
-
-
0001553497
-
-
D. W. Brown and M. Jones, Jr.
-
(a) R. Likhotvorik, D. W. Brown and M. Jones, Jr., J. Am. Chem. 'Soc., 1994, 116, 6175;
-
J. Am. Chem. 'Soc., 1994, 116, 6175
-
-
Likhotvorik, R.1
-
34
-
-
37049084634
-
-
Perkin Trans, l, 1993, 405.
-
J. A. Murphy and C. W. Patterson, J. Chem. Soc., Perkin Trans, l, 1993, 405.
-
J. Chem. Soc.
-
-
Murphy, J.A.1
Patterson, C.W.2
-
35
-
-
33746453567
-
-
John Wiley and Sons, New York, 1987, eh. 21, p. 1223.
-
B. Haiton and M. G. Banwell, The Chemistry of the Cyclopropyl Group; ed. Z. Rappoport, John Wiley and Sons, New York, 1987, eh. 21, p. 1223.
-
The Chemistry of the Cyclopropyl Group; Ed. Z. Rappoport
-
-
Haiton, B.1
Banwell, M.G.2
-
39
-
-
0013490058
-
-
see: M. J. Bennett, J. T. Purdham, S. Takada and S. Masamune
-
For example, see: M. J. Bennett, J. T. Purdham, S. Takada and S. Masamune, J. Am. Chem. Soc., 1971, 93, 4063 and ref. 12b.
-
J. Am. Chem. Soc., 1971, 93, 4063 and Ref. 12b.
-
-
Example, F.1
-
42
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33746397392
-
-
It is interesting to note that la reacts with 1 equiv. of MeLi and then benzaldehyde to afford the corresponding alcohol. Further treatment of this compound with 2 equiv. of MeLi and PhCHO, however, did not afford lOa.
-
It is interesting to note that la reacts with 1 equiv. of MeLi and then benzaldehyde to afford the corresponding alcohol. Further treatment of this compound with 2 equiv. of MeLi and PhCHO, however, did not afford lOa.
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