ADDITION-REACTION OF PHENYL ISOCYANATE AND PHENYL ISOTHIOCYANATE TO PARTIALLY CYCLIC 1,3-DIAZA-1,3-BUTADIENES - SYNTHESIS OF ANNULATED 1,3,5-TRIAZINE-2,4(1H,3H)-DIONES AND 1,3,5-TRIAZINE-2,4(1H,3H)-DITHIONES

被引：4

作者：

ABDELRAHMAN, MA

机构：

[1] Department of Chemistry, Faculty of Science, Sohag University, Sohag

来源：

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 1993年 / 66卷 / 02期

关键词：

D O I：

10.1246/bcsj.66.510

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Annulated 1,3,5-triazine-2,4(1H,3H)-diones and -2,4(1H,3H)-dithiones (8 and 9) are synthesized by a 4pi+2pi cyclodimerization of heterocyclic heterocurnulenes (6 and 7). These heterocumulenes are generated from partially cyclic 1,3-diaza-1,3-butadienes (1a-c) by means of a 2pi+2pi cycloaddition reaction with phenyl isocyanate or phenyl isothiocyanate and followed by dissociation of the resulting cycloadducts (1,3-diazetidinones (3) and 1,3-diazetidithiones (4)).

引用

页码：510 / 512

页数：3

共 23 条

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BOGER, DL
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[7] A STEREOSELECTIVE TOTAL SYNTHESIS OF EPI-LUPININE
BREMMER, ML
WEINREB, SM
[J]. TETRAHEDRON LETTERS, 1983, 24 (03) : 261 - 264
[8] CHERKASOV VM, 1969, CHEM HETEROCYCL COMP, P266
[9] GIZYCKI UV, 1968, ANGEW CHEM INT EDIT, V7, P381
[10] GIZYCKI UV, 1968, ANGEW CHEM INT EDIT, V7, P380

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