A general method of preparation of N-diformylmethylazoles and cycloimonium diformyl methylides Full article
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ChemPlusChem
ISSN: 1212-6950 , E-ISSN: 0010-0765 |
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| Output data | Year: 1988, Volume: 53, Number: 7, Pages: 1519-1528 Pages count : 10 DOI: 10.1135/cccc19881519 | ||||
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Abstract:
Formylation of easily accessible heteroarylacetic acids (R-CH2COOH, R = imidazole, pyrazole, tetrazole, pyridine) afforded in high yields the corresponding trimethinium salts R-C(=CH-N(CH3)2)CH=N(CH3)2)n+ nX- which on alkaline hydrolysis were converted into N-diformylmethylazoles R-C(CHO)=CH-OH. Their quaternization gave cycloimonium diformyl methylides.
Cite:
Král V.
, Semenov V.V.
, Kanishchev M.I.
, Arnold Z.
, Shevelev S.A.
, Fainzilberg A.A.
A general method of preparation of N-diformylmethylazoles and cycloimonium diformyl methylides
ChemPlusChem. 1988. V.53. N7. P.1519-1528. DOI: 10.1135/cccc19881519 OpenAlex
A general method of preparation of N-diformylmethylazoles and cycloimonium diformyl methylides
ChemPlusChem. 1988. V.53. N7. P.1519-1528. DOI: 10.1135/cccc19881519 OpenAlex
Identifiers:
| ≡ OpenAlex: | W2047192859 |