Access to 2,3-diaryl-4-nitrothiochroman S,S-dioxides from 3-nitrobenzo[b]thiophene

Author:

Bianchi Lara,Maccagno Massimo,Petrillo Giovanni,Rizzato Egon,Sancassan Fernando,Spinelli Domenico,Tavani Cinzia

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Bianchi, L.; Maccagno, M.; Petrillo, G.; Sancassan, F.; Spinelli, D.; Tavani, C. ‘2,3-Dinitro-1,3-butadienes: versatile Building-blocks from the Ring Opening of 3,4-dinitrothiophene’ in Targets in Heterocyclic Systems—Chemistry and Properties, SocietàChimicaItaliana: Rome; 2006, Vol. 10, pp 1–23.

2. Bianchi, L.; Maccagno, M.; Petrillo, G.; Rizzato, E.; Sancassan, F.; Severi, E.; Spinelli, D.; Tavani, C.; Viale, M. ‘Versatile Nitrobutadienic Building-blocks from the Ring Opening of 2- and 3-nitrothiophenes’ in Targets in Heterocyclic Systems—Chemistry and Properties, SocietàChimicaItaliana: Rome; 2007, Vol. 11, pp 1–20.

3. Nitrobutadienes from ß-nitrothiophenes: valuable building-blocks in the overall ring-opening / ring-closure protocol to homo- or hetero-cycles

4. Easy access to 4-nitrothiochroman S,S-dioxides via ring-enlargement from 3-nitrobenzo[b]thiophene

5. Ring-Opening/Ring-Closing Protocols from Nitrothiophenes: Six-Membered versus Unusual Eight-Membered Sulfur Heterocycles through Michael-Type Addition on Nitrobutadienes

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