Condensation of ethyl esters of 6-phenyl-and 6-(p-methoxyphenyl)-2,4-dioxocyclo-hexane-1-carboxylic acids with N-benzylidene-2-naphthylamines

1980 ◽  
Vol 16 (7) ◽  
pp. 758-761 ◽  
Author(s):  
N. S. Kozlov ◽  
L. F. Gladchenko ◽  
G. P. Korotyshova
Keyword(s):  
Carboxylic Acids ◽  
Ethyl Esters

The Hantzsch pyrrole synthesis

1970 ◽  
Vol 48 (11) ◽  
pp. 1689-1697 ◽  
Author(s):  
M. W. Roomi ◽  
S. F. MacDonald
Keyword(s):  
Carboxylic Acids ◽  
Ethyl Acetoacetate ◽  
Alkyl Group ◽  
Ethyl Esters ◽  
Hantzsch Synthesis ◽  
Butyl Esters ◽  
Alkyl Groups

Ethyl esters of 2-alkyl- and 2,4-dialkylpyrrole-3-carboxylic acids are obtained generally by extensions of the Hantzsch synthesis, benzyl and t-butyl esters when the 2-alkyl group is methyl. Hemopyrrole is obtained from butanal and ethyl acetoacetate in three steps. Pyrroles bearing higher alkyl groups or carbobenzoxy groups are reductively alkylated like the corresponding methylpyrroles and carbethoxy derivatives; t-butyl esters do not survive.

Photochemistry of ethyl esters of α-oxo-carboxylic acids

1990 ◽  
Vol 53 (1) ◽  
pp. 77-85 ◽  
Author(s):  
A.L. Zanocco ◽  
E.A. Soto ◽  
E.A. Lissi ◽  
J.C. Scaiano
Keyword(s):  
Carboxylic Acids ◽  
Ethyl Esters

Electrochemical fluorination of several methyl and/or ethyl esters of morpholino-substituted carboxylic acids

2001 ◽  
Vol 111 (2) ◽  
pp. 115-128 ◽  
Author(s):  
Takashi Abe ◽  
Hajime Baba ◽  
Kunio Okuhara ◽  
Haruhiko Fukaya
Keyword(s):  
Carboxylic Acids ◽  
Ethyl Esters ◽  
Electrochemical Fluorination

Synthesis of some 1-aryl-1,4-dihydro-4-oxoquinoline-3-carboxylic acids and their antibacterial activity

1989 ◽  
Vol 54 (8) ◽  
pp. 2181-2189 ◽  
Author(s):  
Stanislav Rádl ◽  
Viktor Zikán
Keyword(s):  
Antimicrobial Activity ◽  
Antibacterial Activity ◽  
Carboxylic Acids ◽  
Hydrogen Fluoride ◽  
Ferrous Sulfate ◽  
Ethyl Esters ◽  
Direct Arylation

1,4-Dihydro-4-oxoquinoline-3-carboxylic acids VIIIc and VIIId were prepared via their ethyl esters VIIIa and VIIIb, which were obtained by a direct arylation of ethyl 7-chloro-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (VIa). When treated with piperazine or N-methylpiperazine compound VIIId yields VIIIe or VIIIf, respectively. Reduction of VIIId, VIIIe, and VIIIf with ferrous sulfate yields VIIIg, VIIIh, and VIIIi, respectively. Diazotization and introduction of fluorine into VIIIg using hydrogen fluoride-pyridine yields VIIIj. The compounds prepared were tested for their antimicrobial activity in vitro.

Heat capacity, saturation vapor pressure, and thermodynamic functions of ethyl esters of C3–C5 and C18 carboxylic acids

2011 ◽  
Vol 85 (9) ◽  
pp. 1516-1527 ◽  
Author(s):  
L. E. Agafonova ◽  
R. M. Varushchenko ◽  
A. I. Druzhinina ◽  
O. V. Polyakova ◽  
Yu. S. Kolesov
Keyword(s):  
Heat Capacity ◽  
Vapor Pressure ◽  
Carboxylic Acids ◽  
Thermodynamic Functions ◽  
Ethyl Esters ◽  
Saturation Vapor Pressure ◽  
Saturation Vapor

Iodomethylates of ?-(N-morpholino- and N-pipecolino) ethyl esters of carboxylic acids as substrates of cholinesterase

1983 ◽  
Vol 32 (11) ◽  
pp. 2227-2231 ◽  
Author(s):  
A. A. Abduvakhabov ◽  
M. A. Azlyarova ◽  
A. P. Brestkin ◽  
E. B. Maizel ◽  
E. V. Rozengart ◽  
...  
Keyword(s):  
Carboxylic Acids ◽  
Ethyl Esters ◽  
Esters Of Carboxylic Acids
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