A novel cyclization process of 2,3-bis(trimethylsilyl)buta-1,3-diene with various acyl chlorides in the presence of aluminium trichloride affords 2,5-disubstituted or 2,3,5-trisubstituted furans in short reaction time; a subsequent acylation process of the furan ring occurs if the reaction time is prolonged. © The Royal Society of Chemistry.

A novel cyclization reaction between 2,3-bis(trimethylsilyl)buta-1,3-diene and acyl chlorides with straightforward formation of polysubstituted furans

Cicco Stefania R;
2007

Abstract

A novel cyclization process of 2,3-bis(trimethylsilyl)buta-1,3-diene with various acyl chlorides in the presence of aluminium trichloride affords 2,5-disubstituted or 2,3,5-trisubstituted furans in short reaction time; a subsequent acylation process of the furan ring occurs if the reaction time is prolonged. © The Royal Society of Chemistry.
2007
Inglese
36
3756
3758
http://www.scopus.com/record/display.url?eid=2-s2.0-34548645639&origin=inward
organic chemistry
1
info:eu-repo/semantics/article
262
Babudri, Francesco; Babudri, Francesco; Cicco, Stefania R.; Farinola, Gianluca M.; Lopez, Linda C.; Naso, Francesco; Naso, Francesco; Pinto, Vita...espandi
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/319874
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