Investigations of the reactivity of pyridine carboxylic acids with diazodiphenylmethane in protic and aprotic solvents, Part I: Pyridine mono-carboxylic acids [PDF]
Journal of the Serbian Chemical Society, 2005 Rate constants for the reaction of diazodiphenylmethane with isomeric pyridine carboxylic acids were determined in chosen protic and aprotic solvents at 30 °C, using the well known UV spectrophotometric method.
Marinković Aleksandar D. +3 more
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Investigations of the reactivity of pyridine carboxylic acids with diazodiphenylmethane in protic and aprotic solvents. Part II. Pyridine mono-carboxylic acid N-oxides [PDF]
Journal of the Serbian Chemical Society, 2006 The rate constants for the reaction of three isomeric pyridine mono-carbocylic acid N-oxides with diazodiphenylmethane were determined at 30 ºC in thirty two protic and aprotic solvents by the well known UV spectrophotometric method.
MILICA MISIC-VUKOVIC +3 more
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Chemistry of Heterocyclic Compounds, 1966 A number of amides and hydrazides of 4-phenyl-2,5-pyridine dicarboxylic acids are synthesized. © 1966 The Faraday Press, Inc.
Prostakov N.S. +3 more
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Structural Studies on Solvates of Cyclic Imide Tethered Carboxylic Acids with Pyridine and Quinoline
, 2016 Structures of eight solvates of cyclic imide tethered carboxylic acids and aromatic tetra carboxylic acids with pyridine (solvate I−VI) and quinoline (VII−VIII) are determined.
Devendra Singh (367341) +2 more
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SHORT-CHAIN CARBOXYLIC-ACIDS, A NEW CLASS OF TERATOGENS - STUDIES OF POTENTIAL BIOCHEMICAL-MECHANISMS [PDF]
, 1986 Certain short-chain carboxylic acids (SCCA) appear to share a common teratogenic potential, although the structural requirements for activity remain obscure.
Coakley, ME +5 more
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2-(Phenylsulfanyl)pyridine-3-carboxylic acid [PDF]
Acta Crystallographica Section E Structure Reports Online, 2009 The title compound, C(12)H(9)NO(2)S, belongs to the nitro-gen-containing group of heterocyclic organic compounds and crystallized with two mol-ecules per asymmetric unit. In the crystal, both molecules form investment dimers linked by pairs of O-H-O hydrogen bonds. Weak symmetry-related C-H-O inter-actions link the carboxyl dimers along b axis.
Muhammad Naeem Khan +4 more
openaire +3 more sources
Convenient approaches to the synthesis of 6-amino- and 6-oxoimidazo[4,5-b]pyrazolo[3,4-e]pyridines
Журнал органічної та фармацевтичної хімії, 2021 Aim. To develop convenient approaches to the synthesis of 6-amino- and 6-oxoimidazo[4,5-b]pyrazolo[3,4-e]pyridines as promising biologically active scaffolds. Results and discussion.
Georgiy G. Yakovenko, Mikhailo V. Vovk
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Molecules, 2022 Amides, anhydrides, esters, and thioesters of 2H-azirine-2-carboxylic acids were prepared by a rapid procedure at room temperature involving FeCl2-catalyzed isomerization of 5-chloroisoxazoles to 2H-azirine-2-carbonyl chlorides, followed by reaction with
Anastasiya V. Agafonova +2 more
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Action of Thionyl Chloride on Carboxylic Acids in Presence of Pyridine [PDF]
Nature, 1946 THE catalytic effect of small amounts of pyridine in the reaction between thionyl chloride and carboxylic acids is well known; Carre and Libermann1 have shown further that it is of great advantage to use equimolar quantities of acid, pyridine, and thionyl chloride, the acid chloride then being formed rapidly at lower temperatures, in high yield.
J P E, HUMAN, J A, MILLS
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, 2022 A carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group.
Małgorzata Wolniewicz
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