Pregled bibliografske jedinice broj: 780739
BCl3-Mediated H-Ene Reaction of Sulfur Dioxide and Unfunctionalized Alkenes
BCl3-Mediated H-Ene Reaction of Sulfur Dioxide and Unfunctionalized Alkenes // Chemistry : a European journal, 20 (2010), 5969-5975 doi:10.1002/chem.201000164 (međunarodna recenzija, članak, znanstveni)
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Naslov
BCl3-Mediated H-Ene Reaction of Sulfur Dioxide and Unfunctionalized Alkenes
Autori
Markovic, D. ; Volla, C. M. R. ; Varela-Álvarez, A. ; Sordo, J. A. ; Vogel, P.
Izvornik
Chemistry : a European journal (0947-6539) 20
(2010);
5969-5975
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
sulfinic acid; ene reaction; computation studies
Sažetak
The first ene reactions of SO(2) and unfunctionalized alkenes are reported. Calculations suggest that the endergonic ene reactions of SO(2) with alkenes can be used to generate beta, gamma-unsaturated sulfinyl and sulfonyl compounds. Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. The latter can be reacted with electrophiles to generate sulfones, or with silyl chloride to form beta, gamma-unsaturated silyl sulfinates. The sulfinic acid.BCl(3) complexes can be reacted with ethers that act as oxygen nucleophiles to produce corresponding sulfinic esters. Thus one-pot, three-component synthesis of beta, gamma-unsaturated sulfonamides, sulfinyl esters and sulfones have been developed starting from alkenes and sulfur dioxide (reagent and solvent).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE