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An Efficient Catalytic Method for Regioselective Sulfenylation of Electron‐Rich Aza‐Aromatics at Room Temperature
Author(s) -
Marcantoni Enrico,
Cipolletti Roberto,
Marsili Laura,
Menichetti Stefano,
Properzi Roberta,
Viglianisi Caterina
Publication year - 2013
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201201100
Subject(s) - regioselectivity , chemistry , electrophilic aromatic substitution , catalysis , electrophile , alkyl , organic chemistry , electrophilic substitution , electrophilic addition , combinatorial chemistry
Electron‐rich aza‐aromatic compounds such as indoles and pyrroles are structures of particular interest and importance in organic chemistry. A useful methodology for the regioselective introduction of the sulfenyl group into electron‐rich aza‐aromatics using S ‐alkyl‐ and S ‐arylthiophthalimides as sulfenylating agents is described. Catalytic amounts of CeCl 3 · 7H 2 O/NaI are crucial to the promotion of this regioselective carbon–sulfur‐bond‐forming electrophilic aromatic substitution reaction. The reaction occurred under mild conditions, and the products were obtained in good to excellent yields. The method represents an efficient preparation of sulfenyl aza‐aromatics, which are useful intermediates for important organic transformations, due to the great importance of functionalized indoles among natural compounds and pharmaceutical products.