Thiophosphoric Acid Derivatives of Ethylamine, DL-Methionine, and L-Proline Ethyl Esters II

1962 ◽  
Vol 51 (5) ◽  
pp. 427-431
Author(s):  
Florence C. Klee ◽  
Ernst R. Kirch
Keyword(s):  
Ethyl Esters ◽  
Thiophosphoric Acid ◽  
Derivatives Of

1-Substitution derivatives of 4-aryl-2,3-dibromo-1-naphthol

1981 ◽  
Vol 46 (9) ◽  
pp. 2116-2122 ◽  
Author(s):  
Jiří Křepelka ◽  
Jiří Roubík ◽  
Jiří Holubek
Keyword(s):  
Aqueous Medium ◽  
Ethyl Esters ◽  
Derivatives Of

Alkylation of 7-ethyl-4-(4-ethylphenyl)-2,3-dibromo-1-naphthol (I) with ethyl esters of ω-bromoalkanoic acids XX-XXIII in a non-aqueous medium gave the 1-substitution derivatives II, IV, VI and VIII which were hydrolyzed to the acids III, V, VII and IX. The acid III was used for syntheses of the esters X-XIII and amides XIV-XVIII. Compounds II-XVIII exhibited moderate antineoplastic effects in animals with transplanted tumours; best results were observed with the compound II.

Derivatives of 4-(Aminomethyl)pyrrole-3-carboxylic Acid

1994 ◽  
Vol 47 (5) ◽  
pp. 975 ◽  
Author(s):  
DP Arnold ◽  
RFC Brown ◽  
LJ Nitschinsk ◽  
P Perlmutter ◽  
HK Tope
Keyword(s):  
Carboxylic Acid ◽  
Ethyl Esters ◽  
Tosylmethyl Isocyanide ◽  
Derivatives Of

Methyl and ethyl esters of 4-( aminomethyl )pyrrole-3-carboxylic acid were made through pyrrole synthesis with tosylmethyl isocyanide , but cyclization to a bicyclic lactam (1) was not achieved.

Derivatives of 5α-androstan-3α- and 3β-ol with acrylate side chain

1990 ◽  
Vol 55 (5) ◽  
pp. 1243-1256 ◽  
Author(s):  
Vladimír Pouzar ◽  
Hana Chodounská ◽  
Dalibor Sameš ◽  
Pavel Drašar ◽  
Miroslav Havel
Keyword(s):  
Ethyl Esters ◽  
Side Chain ◽  
Protecting Group ◽  
Derivatives Of

Hydroxy derivatives I, II, III, XVII and XX were oxidized to give the respective aldehydes IV, V, VI, XVIII and XXI which were further converted by Wittig-Horner reaction into unsaturated methyl and ethyl esters. Removal of the acetal protecting group in position 3 afforded methylesters X, XXIV and XXXVI and ethyl esters XIV, XXV and XXXVII. Compounds XXIV, XXV, XXXVI and XXXVII were converted into the corresponding hemisuccinates XXVIII, XXIX, XL and XLI and β-D-glucosides XXXII, XXXIII, XLIV and XLV.

scholarly journals Effects of Ethyl Ester Derivatives of Valproic Acid Metabolites on Pentylenetetrazol Seizures in Mice

1981 ◽  
Vol 8 (3) ◽  
pp. 259-261 ◽  
Author(s):  
J. Bruni ◽  
E.J. Hammond ◽  
B.J. Wilder
Keyword(s):  
Valproic Acid ◽  
Ethyl Ester ◽  
Adult Male ◽  
Anticonvulsant Activity ◽  
Ethyl Esters ◽  
Icr Mice ◽  
Acid Metabolites ◽  
Pentylenetetrazol Seizures ◽  
Derivatives Of

SUMMARY:The anticonvulsant activity of the ethyl esters of the major valproic acid metabolites was assessed against minimal pentylenetetrazol seizures in adult male ICR mice. The ethyl ester 3-hydroxy-propylpentanoic acid was found to possess significant anticonvulsant activity.

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