How steric effects favor thiepins over their benzene sulfide tautomers at theoretical levels?
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics,Biochemistry
Reference20 articles.
1. Synthesis of 2,7-di-tert-butyl-4-ethoxycarbonyl-5-methylthiepin. A remarkably stable and simple monocyclic thiepin
2. Facile bridge expulsion of sulfur heterocycles. 7-Thiabicyclo[2.2.1]hepta-2,5-diene and 7-thiabicyclo[4.1.0]hepta-2,4-diene systems in thiepin synthesis
3. Notes - On the Constitution of the Condensation Product of o-Phthalaldehyde with Diethyl 2,2'-Thiodiacetate
4. Electronic structure and thermal stability of thiepins. Photoelectron spectroscopic investigations
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