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Titolo:
SYNTHESIS OF 2,6-DISUBSTITUTED 5-AMINOPYRIMIDIN-4-ONES FROM 2,6-DISUBSTITUTED 5-ACETYLPYRIMIDIN-4-ONE OXIMES THROUGH BECKMANN REARRANGEMENT
Autore:
YAMAMOTO Y; OGAWA Y;
Indirizzi:
TOHOKU COLL PHARMACEUT SCI,AOBA KU,4-1 KOMATSUSHIMA 4-CHOME SENDAI MIYAGI 981 JAPAN
Titolo Testata:
Yakugaku zasshi
fascicolo: 3, volume: 115, anno: 1995,
pagine: 256 - 260
SICI:
0031-6903(1995)115:3<256:SO25F2>2.0.ZU;2-K
Fonte:
ISI
Lingua:
ENG
Keywords:
5-ACETYLPYRIMIDIN-4-ONE; 5-ACETYLPYRIMIDIN-4-ONE OXIME; BECKMANN REARRANGEMENT; 5-ACETYLAMINOPYRIMIDIN-4-ONE; PYRIMIDO[5,4-B]ISOXAZOLINE;
Tipo documento:
Note
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
7
Recensione:
Indirizzi per estratti:
Citazione:
Y. Yamamoto e Y. Ogawa, "SYNTHESIS OF 2,6-DISUBSTITUTED 5-AMINOPYRIMIDIN-4-ONES FROM 2,6-DISUBSTITUTED 5-ACETYLPYRIMIDIN-4-ONE OXIMES THROUGH BECKMANN REARRANGEMENT", Yakugaku zasshi, 115(3), 1995, pp. 256-260

Abstract

2,6-Disubstituted 5-acetylpyrimidin-4-one oximes were heated in formic acid under reflux to undergo Beckmann rearrangement, giving 2,6-disubstituted 5-acetylaminopyrimidin-4-ones (5a-d) in good yields.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/11/17 alle ore 05:51:33