Literature DB >> 19053614

The endocyclic restriction test: the geometries of nucleophilic substitutions at sulfur(VI) and sulfur(II).

Stephen G Jarboe1, Michael S Terrazas, Peter Beak.   

Abstract

The trajectories for nucleophilic substitutions at sulfur(VI) and sulfur(II) have been investigated by the endocyclic restriction test. On the basis of double-labeling experiments, the sulfur(VI) transfer in the conversion of 1 to 2 is found to be intramolecular, while the sulfur(VI) transfer in the conversion of 3 to 4 and the sulfur(II) transfer in the conversion of 5 to 6 are found to be intermolecular. These results are taken to be consistent with transition structures for these sulfur transfer reactions which require a large angle between the entering and leaving group, a geometry analogous to apical group positions in trigonal bipyramidal transition states.

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Year:  2008        PMID: 19053614     DOI: 10.1021/jo8016428

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

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2.  Synthesis and Sulfur Electrophilicity of the Nuphar Thiaspirane Pharmacophore.

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Journal:  RSC Adv       Date:  2018-01-22       Impact factor: 4.036

  3 in total

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