PREPARATION AND CONFORMATIONAL-ANALYSIS OF 6,10-DISUBSTITUTED [1,2,3]TRITHIOLO[H]BENZOPENTATHIEPIN MONOOXIDES

Citation
T. Kimura et al., PREPARATION AND CONFORMATIONAL-ANALYSIS OF 6,10-DISUBSTITUTED [1,2,3]TRITHIOLO[H]BENZOPENTATHIEPIN MONOOXIDES, Tetrahedron letters, 38(9), 1997, pp. 1607-1610
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
38
Issue
9
Year of publication
1997
Pages
1607 - 1610
Database
ISI
SICI code
0040-4039(1997)38:9<1607:PACO6[>2.0.ZU;2-F
Abstract
6,10-Diethyl[1,2,3]trithiolo[h]benzopentathiepin was oxidized with mCP BA (1 eq.) to produce four monooxides, 6,10-diethyl[1,2,3]trithiolo[h] benzopentathiepin 8-oxides and 6,10-diethyl[1,2,3]trithiolo[h]benzopen tathiepin 7-oxides. The structure of the four monooxides obtained was determined by X-ray crystallography. The activation parameters, Delta G(double dagger), Delta H-double dagger, and Delta S-double dagger of these compounds with respect to the inversion of their pentathiepin ri ngs were determined by the results of H-1-NMR spectroscopy. (C) 1997 E lsevier Science Ltd.