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Expedient Synthesis of 1,2‐Thiaborines by Means of Sulfur Insertion into Boroles
Author(s) -
Yruegas Sam,
Martin Caleb D.
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201604638
Subject(s) - sulfur , ring (chemistry) , benzene , molecule , chemistry , character (mathematics) , combinatorial chemistry , aromaticity , computational chemistry , stereochemistry , organic chemistry , mathematics , geometry
The propensity of boroles to undergo ring expansion reactions has been exploited as a route to generate 1,2‐thiaborines, molecules that can be viewed as hybrid inorganic/organic analogues of benzene. Computational studies as well as structural data indicate that the species reported here have a high degree of aromatic character.
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