Quantum chemical calculations on S-centered 1,3-dipoles. 2. Reactivity of thiocarbonyl S-imides in pericyclic reactions

Polish Journal of Chemistry

Volumn 73, Issue 4, 1999, Pages 683-692

  Mloston G ^a   Fabian, J ^b  

^a UNIVERSITY OF LODZ   (Poland)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

Author keywords

3+2 cycloaddition; ab initio quantum chemistry; Density functional theory; Pericyclic reactions; Sulfur extrusion; Thiaziridines; Thiocarbonyl S imides; Valence isomerization

Indexed keywords

EID: 0033238647     PISSN: 01375083     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (30)

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2. We adhere to the traditional and convenient names of the compounds according to the additive nomenclature (cf. Glossary of Class Names of Organic Compounds and Reactive Intermediates on Structure, Pure Appl. Chem., 67, 1368 (1995). The names do not adequately reflect the real electronic structure. An alternative nomenclature is based on the assumption that the structure is fully zwitterionic. This nomenclature refers to ionic fragments defined by IUPAC recommendations as detailed in Pure Appl. Chem., 65, 1358 (1993). This class names are given in parentheses.
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