Literature DB >> 30537384

Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles.

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  2 in total

1.  Versatile Dibenzothio[seleno]phenes via Hexadehydro-Diels-Alder Domino Cyclization.

Authors:  Baohua Liu; Qiong Hu; Yinshan Wen; Bo Fang; Xiaoliang Xu; Yimin Hu
Journal:  Front Chem       Date:  2019-05-24       Impact factor: 5.221

2.  Halogenation Reactions of Alkyl Alcohols Employing Methyl Grignard Reagents.

Authors:  Nadia Hirbawi; Patricia C Lin; Elizabeth R Jarvo
Journal:  J Org Chem       Date:  2022-09-01       Impact factor: 4.198

  2 in total

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