-
1
-
-
12044258141
-
Prostaglandins Leukotrienes and other Eicosanoids. From Biogenesis to Clinical Applications
-
Reviews: (a). F. Marks, & G. Fürstenberger. Wiley-VCH, Weinheim
-
Reviews: (a) Marks F., Fürstenberger G. Prostaglandins Leukotrienes and other Eicosanoids. From Biogenesis to Clinical Applications. 1999;Wiley-VCH, Weinheim, (b) Collins P.W., Djuric S.W. Chem. Rev. 93:1993;1533.
-
(1993)
Chem. Rev.
, vol.93
, pp. 1533
-
-
Collins, P.W.1
Djuric, S.W.2
-
4
-
-
0019446409
-
-
Goldstein S., Vannes P., Houge C., Hesbain-Frisque A.M., Wiaux-Zamar C., Ghosez L., Germain G., Declercq J.P., Van Meersche M., Arrieta J.M. J. Am. Chem. Soc. 103:1981;4616.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 4616
-
-
Goldstein, S.1
Vannes, P.2
Houge, C.3
Hesbain-Frisque, A.M.4
Wiaux-Zamar, C.5
Ghosez, L.6
Germain, G.7
Declercq, J.P.8
Van Meersche, M.9
Arrieta, J.M.10
-
5
-
-
0001649302
-
-
(a) Marko I., Ronsmans B., Hesbain-Frisque A.M., Dumas S., Ghosez L., Ernst B., Greuter H. J. Am. Chem. Soc. 107:1985;2192.
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 2192
-
-
Marko, I.1
Ronsmans, B.2
Hesbain-Frisque, A.M.3
Dumas, S.4
Ghosez, L.5
Ernst, B.6
Greuter, H.7
-
6
-
-
1542496403
-
-
(b) Review:
-
(b) Review: Snider B. Chem. Rev. 88:1988;793-797.
-
(1988)
Chem. Rev.
, vol.88
, pp. 793-797
-
-
Snider, B.1
-
9
-
-
0037008560
-
-
and references cited therein
-
(c) Ghosez L., Mahuteau-Betzer F., Génicot C., Vallribera A., Cordier J.F. Chem. Eur. J. 8:2002;3411. and references cited therein.
-
(2002)
Chem. Eur. J.
, vol.8
, pp. 3411
-
-
Ghosez, L.1
Mahuteau-Betzer, F.2
Génicot, C.3
Vallribera, A.4
Cordier, J.F.5
-
11
-
-
0024590410
-
-
(2S,5S)-Dimethylpyrrolidine was prepared in 100 g batches from (2R,5R)-hexanediol following the general procedure described by Masamune et al. (a) Short R.P., Kennedy R.M., Masamune S. J. Org. Chem. 54:1989;1755. The diol was obtained from the reduction of 2,5-hexanedione (b) Lieser J.K. Synth. Commun. 13:1983;765 (c) Kruizinga W.H., Strijveen B., Kellog R.M. J. Org. Chem. 46:1981;4321. Or by a Kolbe reaction on (3R)-3-hydroxybutyric acid (d) Burk M.J., Feaster J.E., Horlow J.T. Tetrahedron: Asymmetry. 2:1991;529.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 1755
-
-
Short, R.P.1
Kennedy, R.M.2
Masamune, S.3
-
12
-
-
0000956274
-
-
(2S,5S)-Dimethylpyrrolidine was prepared in 100 g batches from (2R,5R)-hexanediol following the general procedure described by Masamune et al. (a) Short R.P., Kennedy R.M., Masamune S. J. Org. Chem. 54:1989;1755. The diol was obtained from the reduction of 2,5-hexanedione (b) Lieser J.K. Synth. Commun. 13:1983;765 (c) Kruizinga W.H., Strijveen B., Kellog R.M. J. Org. Chem. 46:1981;4321. Or by a Kolbe reaction on (3R)-3-hydroxybutyric acid (d) Burk M.J., Feaster J.E., Horlow J.T. Tetrahedron: Asymmetry. 2:1991;529.
-
(1983)
Synth. Commun.
, vol.13
, pp. 765
-
-
Lieser, J.K.1
-
13
-
-
0000588080
-
-
(2S,5S)-Dimethylpyrrolidine was prepared in 100 g batches from (2R,5R)-hexanediol following the general procedure described by Masamune et al. (a) Short R.P., Kennedy R.M., Masamune S. J. Org. Chem. 54:1989;1755. The diol was obtained from the reduction of 2,5-hexanedione (b) Lieser J.K. Synth. Commun. 13:1983;765 (c) Kruizinga W.H., Strijveen B., Kellog R.M. J. Org. Chem. 46:1981;4321. Or by a Kolbe reaction on (3R)-3-hydroxybutyric acid (d) Burk M.J., Feaster J.E., Horlow J.T. Tetrahedron: Asymmetry. 2:1991;529.
-
(1981)
J. Org. Chem.
, vol.46
, pp. 4321
-
-
Kruizinga, W.H.1
Strijveen, B.2
Kellog, R.M.3
-
14
-
-
85031143849
-
-
(2S,5S)-Dimethylpyrrolidine was prepared in 100 g batches from (2R,5R)-hexanediol following the general procedure described by Masamune et al. (a). The diol was obtained from the reduction of 2,5-hexanedione (b). Or by a Kolbe reaction on (3R)-3-hydroxybutyric acid (d)
-
(2S,5S)-Dimethylpyrrolidine was prepared in 100 g batches from (2R,5R)-hexanediol following the general procedure described by Masamune et al. (a) Short R.P., Kennedy R.M., Masamune S. J. Org. Chem. 54:1989;1755. The diol was obtained from the reduction of 2,5-hexanedione (b) Lieser J.K. Synth. Commun. 13:1983;765 (c) Kruizinga W.H., Strijveen B., Kellog R.M. J. Org. Chem. 46:1981;4321. Or by a Kolbe reaction on (3R)-3-hydroxybutyric acid (d) Burk M.J., Feaster J.E., Horlow J.T. Tetrahedron: Asymmetry. 2:1991;529.
-
(1991)
Tetrahedron: Asymmetry
, vol.2
, pp. 529
-
-
Burk, M.J.1
Feaster, J.E.2
Horlow, J.T.3
-
16
-
-
85031140297
-
-
The highest enantiomeric excesses obtained by using 1.5 equiv. of various N,N-dialkyl-norephedrines were around 50% in the case of benzaldehyde and around 15% in the case of an achiral aldehyde similar to 4.
-
-
-
-
17
-
-
0001359587
-
-
Hafner A., Duthaler R.O., Marti R., Rihs G., Rothe-Streit P., Scharzenbach F. J. Am. Chem. Soc. 114:1992;2321.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 2321
-
-
Hafner, A.1
Duthaler, R.O.2
Marti, R.3
Rihs, G.4
Rothe-Streit, P.5
Scharzenbach, F.6
-
19
-
-
0018884259
-
-
The conformation of bicyclic cyclobutanones 13-15 were assumed to be identical to similar derivatives analysed by X-ray diffraction analysis (a) Howards C.C., Newton R.F., Reynolds D.P., Wadsworth A.H., Kelly D.R., Roberts S.M. J. Chem. Soc. Perkin Trans. 1. 1980;852 (b) Howards C.C., Newton R.F., Reynolds D.P., Roberts S.M. J. Chem. Soc. Perkin Trans. 1. 1981;2049.
-
(1980)
J. Chem. Soc. Perkin Trans. 1
, pp. 852
-
-
Howards, C.C.1
Newton, R.F.2
Reynolds, D.P.3
Wadsworth, A.H.4
Kelly, D.R.5
Roberts, S.M.6
-
20
-
-
0010340162
-
-
The conformation of bicyclic cyclobutanones
-
The conformation of bicyclic cyclobutanones 13-15 were assumed to be identical to similar derivatives analysed by X-ray diffraction analysis (a) Howards C.C., Newton R.F., Reynolds D.P., Wadsworth A.H., Kelly D.R., Roberts S.M. J. Chem. Soc. Perkin Trans. 1. 1980;852 (b) Howards C.C., Newton R.F., Reynolds D.P., Roberts S.M. J. Chem. Soc. Perkin Trans. 1. 1981;2049.
-
(1981)
J. Chem. Soc. Perkin Trans. 1
, pp. 2049
-
-
Howards, C.C.1
Newton, R.F.2
Reynolds, D.P.3
Roberts, S.M.4
-
21
-
-
0000437994
-
-
Review:
-
Review: Krow G.R. Org. React. 43:1993;251-798.
-
(1993)
Org. React.
, vol.43
, pp. 251-798
-
-
Krow, G.R.1
-
25
-
-
85031133763
-
-
A series of experiments were performed in order to elucidate the origin of this surprising regioselectivity pattern. However they did not lead to any clear-cut explanation
-
A series of experiments were performed in order to elucidate the origin of this surprising regioselectivity pattern. However they did not lead to any clear-cut explanation.
-
-
-
-
32
-
-
0001659326
-
-
Reviews: (a) Tsuji J. Trost B.M. Comprehensive Organic Synthesis. Vol. 7:1991;449-468 Pergamon, Oxford, (b) Tsuji J. Palladium Reagents and Catalysts. 1995;Wiley, New-York. pp 19-30.
-
(1991)
Comprehensive Organic Synthesis
, vol.7
, pp. 449-468
-
-
Tsuji, J.1
-
33
-
-
0003441482
-
-
Reviews: (a). Trost B.M. Pergamon, Oxford. New-York: Wiley
-
Reviews: (a) Tsuji J. Trost B.M. Comprehensive Organic Synthesis. Vol. 7:1991;449-468 Pergamon, Oxford, (b) Tsuji J. Palladium Reagents and Catalysts. 1995;Wiley, New-York. pp 19-30.
-
(1995)
Palladium Reagents and Catalysts
, pp. 19-30
-
-
Tsuji, J.1
|