THE FIRST ISOLATION OF A TELLUROKETONE AND ITS REVERSIBLE DIMERIZATION

Citation
M. Minoura et al., THE FIRST ISOLATION OF A TELLUROKETONE AND ITS REVERSIBLE DIMERIZATION, Tetrahedron letters, 38(14), 1997, pp. 2501-2504
Citations number
34
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
38
Issue
14
Year of publication
1997
Pages
2501 - 2504
Database
ISI
SICI code
0040-4039(1997)38:14<2501:TFIOAT>2.0.ZU;2-1
Abstract
The solid-state thermolysis of a sterically hindered Delta(3)-1,3,4-te lluradiazoline 2 afforded products resulting from intermediary tellone 1 and diazo compound 8 formed by retrocyclization, whereas the flash vacuum thermolysis of 2 led to isolation of tellone 1 as green needles . The spontaneous dimerization of 1 thus obtained occurred in the soli d state to give the corresponding 1,3-ditelluretane 10, which underwen t the thermal cycloreversion in solution to regenerate pure tellone 1. (C) 1997 Elsevier Science Ltd.