Reactions of carbonyl compounds with tervalent phosphorus reagents. Part 7. Benzaldehyde with chlorodiphenylphosphine in the presence of acetic acid

1977 ◽  
pp. 1340 ◽  
Author(s):  
J. Allen Miller ◽  
Denis Stewart
Keyword(s):  
Acetic Acid ◽  
Carbonyl Compounds

scholarly journals Oxidation of Aliphatic Secondary and Benzylic Alcohols to Carbonyl Compounds by Peracetic Acid in the Presence of Sodium Bromide in Acetic Acid

1987 ◽  
Vol 60 (11) ◽  
pp. 4143-4144 ◽  
Author(s):  
Takashi Morimoto ◽  
Masao Hirano ◽  
Hiroyuki Ashiya ◽  
Hidetaka Egashira ◽  
Xiumin Zhuang
Keyword(s):  
Acetic Acid ◽  
Peracetic Acid ◽  
Carbonyl Compounds ◽  
Sodium Bromide ◽  
Benzylic Alcohols

scholarly journals Kinetics and mechanism of the Oxidative regeneration of Carbonyl Compounds from Phenylhydrazones by Tetramminecopper(2+) Bis (Permanganate)

2003 ◽  
Vol 2003 (4) ◽  
pp. 184-185
Author(s):  
Raghvendra Shukla ◽  
László Kótai ◽  
Pradeep K. Sharma ◽  
Kalyan K. Banerji
Keyword(s):  
Acetic Acid ◽  
Carbonyl Compounds ◽  
Kinetics And Mechanism ◽  
Aqueous Acetic Acid ◽  
Acid Proceeds ◽  
Oxidative Regeneration ◽  
Rate Determining Step ◽  
Activated Complex

The oxidation of aldo- and keto-phenylhydrazones by tetraamminecopper(2+) bis(permanganate) (TACP), in aqueous acetic acid, proceeds through a mechanism involving the formation of a cyclic activated complex, in the rate-determining step.

Reactions of the α-carbanion species of (phenylthio)acetic acid and its ester with carbonyl compounds

1978 ◽  
pp. 214-224 ◽  
Author(s):  
Shûichi Yamagiwa ◽  
Nobuto Hoshi ◽  
Hitoshi Sato ◽  
Hiroshi Kosugi ◽  
Hisachi Uda
Keyword(s):  
Acetic Acid ◽  
Carbonyl Compounds

Palladium-Catalyzed Silver-Mediated α-Arylation of Acetic Acid: A New Approach for the α-Arylation of Carbonyl Compounds

ChemCatChem ◽  
2014 ◽  
Vol 6 (6) ◽  
pp. 1589-1593 ◽  
Author(s):  
Guo-Jie Wu ◽  
Jing Guan ◽  
Fu-She Han ◽  
Yu-Long Zhao
Keyword(s):  
Acetic Acid ◽  
Carbonyl Compounds ◽  
New Approach ◽  
Palladium Catalyzed

scholarly journals FLUORESCENCE HISTOCHEMISTRY OF BIOGENIC MONOAMINES A STUDY OF THE CAPACITY OF VARIOUS CARBONYL COMPOUNDS TO FORM FLUOROPHORES WITH BIOGENIC MONOAMINES IN GAS PHASE REACTIONS

1972 ◽  
Vol 20 (6) ◽  
pp. 435-444 ◽  
Author(s):  
STURE AXELSSON ◽  
ANDERS BJÖRKLUND ◽  
OLLE LINDVALL
Keyword(s):  
Acetic Acid ◽  
Gas Phase ◽  
Carbonyl Compounds ◽  
Glyoxylic Acid ◽  
Histochemical Demonstration ◽  
High Reactivity ◽  
Gas Phase Reactions ◽  
Cyclization Reactions ◽  
Biogenic Monoamines ◽  
Keto Acids

The capacity of biogenic amines to form fluorophores in histochemical gas phase reactions has been tested with 20 compounds having a carbonyl group (> C = O) as a common characteristic. Significant visible fluorescence was induced from catecholamines and indolamines with aldehydes, ketones, α-keto acids and carboxylic acids, suggesting that all of these compounds can enter fluorophore-forming cyclization reactions under the histochemical gas phase conditions. The most "reactive" reagents are found among the low molecular aldehydes, and formaldehyde and glyoxylic acid seem to be the most suitable reagents, combining high reactivity with good selectivity. Fluorescence, interesting for the histochemical demonstration of N-acetylated indolamines, was obtained from melatonin and N-acetyl-5-hydroxytryptamine with some acid reagents (glyoxylic acid, formic acid, acetic acid and pyruvic acid). A direct cyclodehydration according to the classical Bischler-Napieralski reaction is the most likely mechanism underlying this fluorophore formation. The usefulness of the various carbonyl reagents for the fluorescence histochemical demonstration of other biologically interesting amines, such as histamine, p-tyramine and octopamine, has been specially investigated.

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