FAJKUSOVÁ, Dagmar and Pavel PAZDERA. 2-Aminothiophenol and Its Disulfide Addition to Acylisothiocyanates. Extension to Selenium Derivatives. (2-Aminothiophenol and Its Disulfide Addition to Acylisothiocyanates. Extension to Selenium Derivatives). In Book of Abstracts. 1st ed. Heidelberg, Ruprecht-Karls-Universität: Gesellschaft Deutscher Chemiker, 2004, p. 12-13.
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Basic information
Original name 2-Aminothiophenol and Its Disulfide Addition to Acylisothiocyanates. Extension to Selenium Derivatives.
Name in Czech Adice 2-aminothiofenolu a jeho disulfidu na acylisothiokyanáty. Reakce derivátů selenu.
Authors FAJKUSOVÁ, Dagmar (203 Czech Republic) and Pavel PAZDERA (203 Czech Republic, guarantor).
Edition 1. vyd. Heidelberg, Ruprecht-Karls-Universität, Book of Abstracts, p. 12-13, 2 pp. 2004.
Publisher Gesellschaft Deutscher Chemiker
Other information
Original language English
Type of outcome Proceedings paper
Field of Study 10401 Organic chemistry
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/04:00021283
Organization unit Faculty of Science
Keywords in English nucleophilic addition; cyclization; benzothiazole; benzoselenazole
Tags benzoselenazole, benzothiazole, cyclization, nucleophilic addition
Tags International impact, Reviewed
Changed by Changed by: doc. RNDr. Pavel Pazdera, CSc., učo 2276. Changed: 9/9/2008 13:32.
Abstract
Nucleophilic addition of 2-aminothiophenol to acylisothiocyanates leading to thioureas, which undergo a cyclization reaction and corresponding benzothiazole derivatives are obtained.
Abstract (in Czech)
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MSM 143100011, plan (intention)Name: Struktura a vazebné poměry, vlastnosti a analýza syntetických a přírodních molekulových ansamblů
Investor: Ministry of Education, Youth and Sports of the CR, Structure and character of bonding, properties and analysis of synthetic and natural molecular ensembles
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