1980
DOI: 10.1016/0040-4020(80)85042-3
|View full text |Cite
|
Sign up to set email alerts
|

Facile oxidative conversion of hydrazides of carboxylic acids to corresponding acids, esters and amides using copper compounds

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
26
0

Year Published

1983
1983
2015
2015

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 48 publications
(27 citation statements)
references
References 10 publications
1
26
0
Order By: Relevance
“…1131 Catalytic amounts of Cu(OAc) 2 with continuous bubbling of oxygen through a methanol solution proved to be effective only for the synthesis of carboxylic acids. For the esters and amides, stoichiometric amounts of copper were required.…”
Section: Reactions Of Aminesmentioning
confidence: 99%
“…1131 Catalytic amounts of Cu(OAc) 2 with continuous bubbling of oxygen through a methanol solution proved to be effective only for the synthesis of carboxylic acids. For the esters and amides, stoichiometric amounts of copper were required.…”
Section: Reactions Of Aminesmentioning
confidence: 99%
“…[32][33][34][35][36][37][38] These are as follows: As pseudo-first order conditions could not be applied, the evaluation was based on determining the initial rate 50-51 of absorbance change at 320 nm. [32][33][34][35][36][37][38] These are as follows: As pseudo-first order conditions could not be applied, the evaluation was based on determining the initial rate 50-51 of absorbance change at 320 nm.…”
Section: Resultsmentioning
confidence: 99%
“…[14][15][16] Hypochlorous acid and its conjugate base, hypochlorite ion, are ubiquitous in biological systems. [32][33][34][35][36][37][38] At this point, it should be mentioned that there is an earlier kinetic study published on the reaction between isoniazid and hypochlorite ion in basic medium. [17][18][19][20][21][22] It is the product of the myeloperoxidase-catalyzed oxidation of chloride ion in the presence hydrogen peroxide 17,22 and may react with a whole range of organic and inorganic reactants in the body.…”
Section: Introductionmentioning
confidence: 99%
“…We found that thallium(III) nitrate trihydrate (TTN) transformed hydrazides to the corresponding acid derivatives under mild reaction conditions [5]. The reactions probably proceed via the acyl diimide, postulated earlier [6,7], although the formation of the acyl cation has also been suggested [8,9]. The final product can either be an acid, ester or amide, depending on the selection of nucleophile (Scheme 1).…”
Section: Oxidation Of Hydrazides and Similar Compoundsmentioning
confidence: 94%