-
1
-
-
0003601534
-
-
Merck Co.,Rahway, New Jersey
-
[1] See trimebutine in Merck Index, 11th Ed., p. 1526. Merck Co.,Rahway, New Jersey (1989)
-
(1989)
Merck Index, 11th Ed.
, pp. 1526
-
-
-
2
-
-
0033869678
-
Pharmacokinetics and bioequivalence of two trimebutine formulations in healthy volunteers using desmethyl-trimebutine levels
-
in press
-
[2] Saivin, S., Lavit, M., Michel, F. et al., Pharmacokinetics and Bioequivalence of Two Trimebutine Formulations in Healthy Volunteers Using Desmethyl-trimebutine Levels. Arzneim.-Forsch./Drug Res., in press (2000).
-
(2000)
Arzneim.-Forsch./drug Res.
-
-
Saivin, S.1
Lavit, M.2
Michel, F.3
-
3
-
-
0033943047
-
Determination of trimebutine and desmethyl-trimebutine in human plasma by HPLC
-
in press
-
[3] Lavit, M., Saivin, S., Boudra, H. et al., Determination of Trimebutine and Desmethyl-trimebutine in Human Plasma by HPLC. Arzeinm-Forsch./Drug Res., in press (2000)
-
(2000)
Arzeinm-Forsch./Drug Res.
-
-
Lavit, M.1
Saivin, S.2
Boudra, H.3
-
4
-
-
0017308082
-
Alkylation and Michael additions of glycine ethyl ester. Use in α-amino acid synthesis and as acyl carbanion equivalent
-
[4] Stork, G., Leong, A. Y. N., Touzin, A.-M., Alkylation and Michael Additions of Glycine Ethyl Ester. Use in α-amino Acid Synthesis and as Acyl Carbanion Equivalent. J. Org. Chem. 41, 3491 (1976)
-
(1976)
J. Org. Chem.
, vol.41
, pp. 3491
-
-
Stork, G.1
Leong, A.Y.N.2
Touzin, A.-M.3
-
5
-
-
33845555590
-
A mild and efficient route to Schiff base derivatives of amino acids
-
[5] O'Donnell, M. J., Polt, R. L., A Mild and Efficient Route to Schiff Base Derivatives of Amino Acids. J. Org. Chem. 47, 2663 (1982)
-
(1982)
J. Org. Chem.
, vol.47
, pp. 2663
-
-
O'Donnell, M.J.1
Polt, R.L.2
-
6
-
-
0029038316
-
Diastereoselective alkylation of sultam-derived amino acid aldimines, preparation of Ca-methylated amino acids
-
[6] Ayoub, M., Chassaing, G., Loffet, A., Diastereoselective Alkylation of Sultam-Derived Amino Acid Aldimines, Preparation of Ca-Methylated Amino Acids. Tetrahedron Lett. 36, 4069 (1995)
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 4069
-
-
Ayoub, M.1
Chassaing, G.2
Loffet, A.3
-
7
-
-
0000147109
-
Reaction of Schiff base anions with α,ω-dihaloalkanes: Synthetic route to cyclic α-aminoacid derivatives
-
[7] Joucla, M., El Goumzili, M., Reaction of Schiff Base Anions with α,ω-dihaloalkanes: Synthetic Route to Cyclic α-Aminoacid Derivatives. Tetrahedron Lett. 27, 1681 (1986)
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 1681
-
-
Joucla, M.1
El Goumzili, M.2
-
8
-
-
0003550135
-
-
Georg Thieme Verlag, Stuttgart-New-York
-
[8] Tietzer, L. F., Eicher, T., Reaktionen und Synthesen im Organisch-Chemischen Praktikum und Forschungs-laboratorium, p. 120. Georg Thieme Verlag, Stuttgart-New-York (1991)
-
(1991)
Reaktionen und Synthesen im Organisch-chemischen Praktikum und Forschungs-laboratorium
, pp. 120
-
-
Tietzer, L.F.1
Eicher, T.2
-
9
-
-
0001106559
-
The use of N-formylamino acids in peptide synthesis
-
[9] Sheehan, J. C., Yang, D. D. H., The Use of N-Formylamino Acids in Peptide Synthesis. J. Am. Chem. Soc. 80, 1154 (1957)
-
(1957)
J. Am. Chem. Soc.
, vol.80
, pp. 1154
-
-
Sheehan, J.C.1
Yang, D.D.H.2
-
10
-
-
5244287483
-
Reduction of bile acids and amides with lithium aluminium hydride
-
[10] Wessely, F., Swoboda, W., Reduction of Bile Acids and Amides with Lithium Aluminium Hydride. Monatsh. 82, 437 (1951)
-
(1951)
Monatsh.
, vol.82
, pp. 437
-
-
Wessely, F.1
Swoboda, W.2
-
11
-
-
0008540495
-
The reduction of p-hydroxyformanilide by lithium aluminium hydride to N-methyl-paminophenol
-
[11] Ehrlich, J., The Reduction of p-Hydroxyformanilide by Lithium Aluminium Hydride to N-Methyl-paminophenol. J. Am. Chem. Soc. 70, 2286 (1948)
-
(1948)
J. Am. Chem. Soc.
, vol.70
, pp. 2286
-
-
Ehrlich, J.1
-
12
-
-
33947332318
-
Selective reductions. IX. Reaction of lithium aluminium hydride with selected organic compounds containing representative functional groups
-
[12] Brown, H. C., Weissman, P. M., Yoon, N. M., Selective Reductions. IX. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. J. Am. Chem. Soc. 88, 1458 (1966)
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 1458
-
-
Brown, H.C.1
Weissman, P.M.2
Yoon, N.M.3
-
13
-
-
33947332955
-
Selective Reductions. X. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. Comparison of the Reducing Characteristics of Lithium Aluminium Hydride and its Derivatives
-
[13] Brown, H. C., Yoon, N. M., Selective Reductions. X. Reaction of Lithium Aluminium Hydride with Selected Organic Compounds Containing Representative Functional Groups. Comparison of the Reducing Characteristics of Lithium Aluminium Hydride and its Derivatives. J. Am. Chem. Soc. 88, 1464 (1966)
-
(1966)
J. Am. Chem. Soc.
, vol.88
, pp. 1464
-
-
Brown, H.C.1
Yoon, N.M.2
-
14
-
-
0001087252
-
The reduction of amides to amines via nitriles by lithium aluminium hydride
-
[14] Newnan, M. S., Fugunga, T., The Reduction of Amides to Amines via Nitriles by Lithium Aluminium Hydride. J. Am. Chem. Soc. 82, 693 (1960)
-
(1960)
J. Am. Chem. Soc.
, vol.82
, pp. 693
-
-
Newnan, M.S.1
Fugunga, T.2
-
15
-
-
0001138143
-
Formylation of amines with chloral and reduction of the N-formyl derivatives with lithium aluminium hydride
-
[15] Blicke, F. F., Lu, C. J., Formylation of Amines with Chloral and Reduction of the N-Formyl Derivatives with Lithium Aluminium Hydride. J. Am. Chem. Soc. 73, 3933 (1951)
-
(1951)
J. Am. Chem. Soc.
, vol.73
, pp. 3933
-
-
Blicke, F.F.1
Lu, C.J.2
-
16
-
-
0001183962
-
The formyl group as a hydrogenolyzable protecting group for peptide syntheses
-
[16] Losse, G., Nadolski, D., The Formyl Group as a Hydrogenolyzable Protecting Group for Peptide Syntheses. J. Prakt. Chem. 24, 118 (1964)
-
(1964)
J. Prakt. Chem.
, vol.24
, pp. 118
-
-
Losse, G.1
Nadolski, D.2
|