| Literature DB >> 30537384 |
Peter Franzmann1, Sebastian B Beil1,2, Dieter Schollmeyer1, Siegfried R Waldvogel1,2.
Abstract
A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5 -mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.Entities:
Keywords: C−H activation; cyclization; molybdenum; oxidation; sulfur heterocycles
Year: 2019 PMID: 30537384 DOI: 10.1002/chem.201805938
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236