Published in
Royal Society of Chemistry, New Journal of Chemistry, 13(42), p. 10592-10602
DOI: 10.1039/c8nj00495a
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Structural diversity in the products formed by the reactions of 2-arylselanyl pyridine derivatives and dihalogens
Journal article published in 2018 by
Riccardo Montis 
,
Massimiliano Arca ,
M. Carla Aragoni ,
Alexander J. Blake ,
Carlo Castellano ,
Francesco Demartin ,
Francesco Isaia ,
Vito Lippolis ,
Anna Pintus ,
Eder J. Lenardão ,
Gelson Perin ,
Alice E. O'Connor,
Samuel Thurow
,
Massimiliano Arca ,
M. Carla Aragoni ,
Alexander J. Blake ,
Carlo Castellano ,
Francesco Demartin ,
Francesco Isaia ,
Vito Lippolis ,
Anna Pintus ,
Eder J. Lenardão ,
Gelson Perin ,
Alice E. O'Connor,
Samuel Thurow
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Abstract
The presence of competing donor sites in L1–L4 influences their reactivity towards dihalogens and interhalogens.