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2
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0002446724
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B.M. Trost, I. Fleming, Heathock C.W. Oxford: Pergamon
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Roush W. Trost B.M., Fleming I., Heathock C.W. Comprehensive Organic Synthesis. 2:1991;1 Pergamon, Oxford.
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Comprehensive Organic Synthesis
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Roush, W.1
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4
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0001310946
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Mg: (b)
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(b) Yasuda, H.; Yamauchi, M.; Nakamura, A.; Sei, T.; Kai, Y.; Yasuoka, N.; Kasai, N. Bull. Chem. Soc. Jpn. 1980, 53, 1089. Zn:
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Bull. Chem. Soc. Jpn.
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Yasuda, H.1
Yamauchi, M.2
Nakamura, A.3
Sei, T.4
Kai, Y.5
Yasuoka, N.6
Kasai, N.7
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5
-
-
0022482955
-
-
Zn: (c)
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(c) Ghosez, L.; Marko, I.; Hesbain-Frisque, A. M. Tetrahedron Lett. 1986, 27, 5211.
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Tetrahedron Lett.
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Ghosez, L.1
Marko, I.2
Hesbain-Frisque, A.M.3
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10
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0031577806
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In: (h)
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In: (h) Hirashita, T.; Inoue, S.; Yamamura, H.; Kawai, M.; Araki, S. J. Organomet. Chem. 1997, 549, 305.
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Hirashita, T.1
Inoue, S.2
Yamamura, H.3
Kawai, M.4
Araki, S.5
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12
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-
0343533928
-
-
Only the reactions with prochiral aldehydes were studied, see Ref. 2g.
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Only the reactions with prochiral aldehydes were studied, see Ref. 2g.
-
-
-
-
13
-
-
0000464520
-
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2Zr' chemistry, see: (a)
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2Zr' chemistry, see: (a) Negishi, E.; Takahashi, T. Bull. Chem. Soc. Jpn. 1998, 71, 755.
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(1998)
Bull. Chem. Soc. Jpn.
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Negishi, E.1
Takahashi, T.2
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19
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-
0030607168
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-
and references cited therein
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Wipf P., Jahn H. Tetrahedron. 52:1996;12853. and references cited therein.
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(1996)
Tetrahedron
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Wipf, P.1
Jahn, H.2
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20
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0343969773
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-
The pentadienyl ethers are quite stable compounds, in contrast to the more sensitive pentadienyl bromides.
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The pentadienyl ethers are quite stable compounds, in contrast to the more sensitive pentadienyl bromides.
-
-
-
-
21
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-
0343969772
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-
We have proved that this new procedure is also useful for the preparation of allylzirconiums from allylic ethers.
-
We have proved that this new procedure is also useful for the preparation of allylzirconiums from allylic ethers.
-
-
-
-
22
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-
0343533927
-
-
Compound 5 was easily prepared in two steps by reaction of 3-methyl-2-butenal with vinylmagnesium bromide followed by etherification with BnBr.
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Compound 5 was easily prepared in two steps by reaction of 3-methyl-2-butenal with vinylmagnesium bromide followed by etherification with BnBr.
-
-
-
-
23
-
-
0343533926
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-
note
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2), 125.9 (CH), 127.7 (CH), 128.2 (CH), 134.2 (CH), 140.5 (C).
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-
-
-
24
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0026662563
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Bedford S.B., Bell K.E., Fenton G., Hayes C.J., Knight D.W., Shaw D. Tetrahedron Lett. 33:1992;6511.
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(1992)
Tetrahedron Lett.
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-
Bedford, S.B.1
Bell, K.E.2
Fenton, G.3
Hayes, C.J.4
Knight, D.W.5
Shaw, D.6
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27
-
-
0343097980
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-
The stereochemical assignments for 14-16 were established by analogy to 12.
-
The stereochemical assignments for 14-16 were established by analogy to 12.
-
-
-
-
28
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-
33748737579
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-
Such types of THF derivatives are rare. For the recent syntheses of tetrahydrofurans, see (a)
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Such types of THF derivatives are rare. For the recent syntheses of tetrahydrofurans, see (a) Elliott, M. C. J. Chem. Soc., Perkin Trans. 1 1998, 4175.
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(1998)
J. Chem. Soc., Perkin Trans.
, vol.1
, pp. 4175
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Elliott, M.C.1
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29
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0034707974
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(b) and references cited therein
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(b) Micalizio, G. C.; Roush, W. R. Org. Lett. 2000, 2, 461 and references cited therein.
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Org. Lett.
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Micalizio, G.C.1
Roush, W.R.2
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