DFT study of cycloaddition reaction of isothiocyanates with diazoazoles to 4-imino-4H-pyrazolo[5,1-d] [1,2,3,5]thiatriazines

被引:5
|
作者
Subbotina, Julia O.
Sadchikova, Elena V.
Bakulev, Vasiliy A.
Fabian, Walter M. F.
Herges, Rainer
机构
[1] Urals State Tech Univ, TOSLab, Ekaterinburg 620002, Russia
[2] Karl Franzens Univ Graz, Inst Chem, A-8010 Graz, Austria
[3] Univ Kiel, Inst Organ Chem, D-2300 Kiel, Germany
关键词
pericyclic reactions; dipolar cycloaddition; DFT; ACID; NICS; NBO;
D O I
10.1002/qua.21351
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The mechanism of reaction of isothiocyanates with diazopyrazoles to 4-imino-4H-pyrazolo[5,1-d] [1,2,3,5]thiatriazines was investigated. It was suggested that the reaction proceeds via a pseudopericyclic cycloaddition with activation barrier of similar to 31 kcal mol(-1) (B3LYP/6-31G(*)). The mechanism was confirmed by NBO and ACID schemes. The question of regioselectivity was also explored. It was shown that an acyl substituent on the isothiocyanate led to a stabilization of the final product due to S... O interaction. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:2479 / 2488
页数:10
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