Display options
Cite
McKee ML, Mlostoń G, Urbaniak K, et al. Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl . Beilstein J Org Chem. 2017;13:410-416doi: 10.3762/bjoc.13.44.
McKee, M. L., Mlostoń, G., Urbaniak, K., & Heimgartner, H. (2017). Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl . Beilstein journal of organic chemistry, 13410-416. https://doi.org/10.3762/bjoc.13.44
McKee, Michael L, et al. "Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl ." Beilstein journal of organic chemistry vol. 13 (2017): 410-416. doi: https://doi.org/10.3762/bjoc.13.44
McKee ML, Mlostoń G, Urbaniak K, Heimgartner H. Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl . Beilstein J Org Chem. 2017 Mar 03;13:410-416. doi: 10.3762/bjoc.13.44. eCollection 2017. PMID: 28382179; PMCID: PMC5355913.
Copy Download .nbib Format: NLM
Share it on

Beilstein J Org Chem. 2017 Mar 03;13:410-416. doi: 10.3762/bjoc.13.44. eCollection 2017.

Dimerization reactions of aryl selenophen-2-yl-substituted thiocarbonyl .

Beilstein journal of organic chemistry

Michael L McKee, Grzegorz Mlostoń, Katarzyna Urbaniak, Heinz Heimgartner

Affiliations

  1. Auburn University, Department of Chemistry and Biochemistry, Auburn, AL, 36849, USA.
  2. Department of Organic and Applied Chemistry, University of ?ód?, Tamka 12, PL 91-403 ?ód?, Poland.
  3. Department of Chemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.

PMID: 28382179 PMCID: PMC5355913 DOI: 10.3762/bjoc.13.44

Abstract

An intriguing stepwise diradical mechanism of the dimerization of the reactive intermediate (thiocarbonyl

Keywords: 1,3-dipolar cycloadditions; reaction mechanisms; reactive intermediates; thiocarbonyl S-methanides; thioketones

References

  1. J Am Chem Soc. 2003 Nov 26;125(47):14425-34 - PubMed
  2. J Phys Chem B. 2009 May 7;113(18):6378-96 - PubMed
  3. J Org Chem. 2015 Dec 18;80(24):12321-32 - PubMed

Publication Types