ACYLATION OF NITROGEN HETEROCYCLES UNDER CONDITIONS OF SCHOTTEN-BAUMANN REACTION .3. IMIDAZOLES

被引：13

作者：

BABAD, E

BENISHAI, D

机构：

[1] Department of Chemistry, Technion - Israel Institute of Technology, Haifa

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 1969年 / 6卷 / 02期

关键词：

D O I：

10.1002/jhet.5570060215

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Imidazole and five N‐monoalkylimidazoles were tested for their ability to undergo ring fission on carbobenzoxylation. Reaction occurred only with imidazoles substituted with strong electron withdrawing groups such as nitrophenyl, dinitrophenyl and monocarbobenzoxy. Copyright © 1969 Journal of Heterocyclic Chemistry

引用

页码：235 / &

共 7 条

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ALTMAN, J
BENISHAI, D
[J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1968, 5 (05) : 679 - &
[2] BENISHAI D, 1968, ISRAEL J CHEM, V6, P551
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Pyman, FL
[J]. JOURNAL OF THE CHEMICAL SOCIETY, 1930, : 397 - 403
[4] STUDIES ON IMIDAZOLE COMPOUNDS .1. A SYNTHESIS OF IMIDAZOLES WITH FUNCTIONAL GROUPS IN THE 2-POSITION
JONES, RG
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1949, 71 (02) : 383 - 386
[5] SYNTHESE VON CARBONSAUREESTERN NACH DER IMIDAZOLIDMETHODE
STAAB, HA
MANNSCHRECK, A
[J]. CHEMISCHE BERICHTE-RECUEIL, 1962, 95 (05): : 1284 - +
[6] Wohl A., 1889, BER DTSCH CHEM GES, V22, P568
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