-
3
-
-
0001884886
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-
Allevi P., Anastasia M., Ciuffreda P., Fiecchi A., Scala A. J. Chem. Soc., Chem. Commun. 1988;57-58.
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(1988)
J. Chem. Soc., Chem. Commun.
, pp. 57-58
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-
Allevi, P.1
Anastasia, M.2
Ciuffreda, P.3
Fiecchi, A.4
Scala, A.5
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7
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-
85031084888
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-
(b) Orsini, F.; Pulici, M. In Trends in Organometallic Chemistry; Menon, J., Ed. Highlights on Recent Advancements in Reformatsky-type Reactions: the Cobalt Approach; Research Trends Pub.: New Delhi, 1994; Vol. 1, pp. 625-667.
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Trends in Organometallic Chemistry
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-
Orsini, F.1
Pulici, M.2
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8
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-
0001386421
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Highlights on recent advancements in reformatsky-type reactions: The cobalt approach
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New Delhi
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Orsini, F.; Pulici, M. In Trends in Organometallic Chemistry; Menon, J., Ed. Highlights on Recent Advancements in Reformatsky-type Reactions: the Cobalt Approach; Research Trends Pub.: New Delhi, 1994; Vol. 1, pp. 625-667.
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(1994)
Research Trends Pub.
, vol.1
, pp. 625-667
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-
Menon, J.1
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12
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-
85031066726
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-
4 is a well-identified complex, that can be conveniently obtained by reducing a mixture of Co(II)-chloride and trimethylphosphine (1:4 mole ratio) with magnesium metal in tetrahydrofuran.
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4 is a well-identified complex, that can be conveniently obtained by reducing a mixture of Co(II)-chloride and trimethylphosphine (1:4 mole ratio) with magnesium metal in tetrahydrofuran.
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-
-
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13
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-
85031068912
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-
Triphenylphosphine can be used as well (albeit the complex formation is somewhat slower), without affecting the course of the reaction.
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Triphenylphosphine can be used as well (albeit the complex formation is somewhat slower), without affecting the course of the reaction.
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-
-
-
16
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-
0028938154
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-
For the ethyl ester, see:
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For the ethyl ester, see: HesKamp B.M., Veeneman G.H., Van der Marel G.A., Van Boeckel C.A.A., Van Boom J.H. Tetrahedron. 51:1995;5657-5670.
-
(1995)
Tetrahedron
, vol.51
, pp. 5657-5670
-
-
HesKamp, B.M.1
Veeneman, G.H.2
Van der Marel, G.A.3
Van Boeckel, C.A.A.4
Van Boom, J.H.5
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17
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-
0343488332
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-
Csuk, R.; Schroder, C.; Krieger C. Tetrahedron 1997, 53, 12947-12960. For ethyl ester, see Ref. 9.
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(1997)
Tetrahedron
, vol.53
, pp. 12947-12960
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-
Csuk, R.1
Schroder, C.2
Krieger, C.3
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21
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37049072340
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Allevi P., Ciuffreda P., Colombo D., Monti D., Speranza G., Manitto P. J. Chem. Soc., Perkin Trans. 1. 1989;1281-1283.
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(1989)
J. Chem. Soc., Perkin Trans. 1
, pp. 1281-1283
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-
Allevi, P.1
Ciuffreda, P.2
Colombo, D.3
Monti, D.4
Speranza, G.5
Manitto, P.6
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22
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85031077480
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unpublished results
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Orsini, F., unpublished results.
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-
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Orsini, F.1
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26
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0027325943
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Moore B.S., Cho H., Casati R., Kennedy E., Reynoldss K.A., Mocek U., Beale J.M., Floss H.G. J. Am. Chem. Soc. 115:1993;5254-5266.
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(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 5254-5266
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-
Moore, B.S.1
Cho, H.2
Casati, R.3
Kennedy, E.4
Reynoldss, K.A.5
Mocek, U.6
Beale, J.M.7
Floss, H.G.8
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32
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85031078636
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Magnesium was activated by adding a few drops of 1,2-dichloroethane to metal turnings (0.5 g) in tetrahydrofuran (3 mL) so that a vigorous reaction ensued. After a few minutes the mixture was ice-cooled, the solvent was removed and the magnesium was washed three times with tetrahydrofuran (2 mL each time).
-
Magnesium was activated by adding a few drops of 1,2-dichloroethane to metal turnings (0.5 g) in tetrahydrofuran (3 mL) so that a vigorous reaction ensued. After a few minutes the mixture was ice-cooled, the solvent was removed and the magnesium was washed three times with tetrahydrofuran (2 mL each time).
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-
-
-
33
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-
85031079796
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-
The solution can also be warmed with an external bath at ca. 50°C to speed the reduction of Co(II) to Co(0). Warming may be useful when triphenylphosphine is used instead of trimethylphosphine.
-
The solution can also be warmed with an external bath at ca. 50°C to speed the reduction of Co(II) to Co(0). Warming may be useful when triphenylphosphine is used instead of trimethylphosphine.
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-
-
-
34
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85031077344
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-
Magnesium metal is used in excess and can be recycled after use.
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Magnesium metal is used in excess and can be recycled after use.
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