61836-14-4Relevant academic research and scientific papers
A modular and scalable one-pot synthesis of polysubstituted furans
Fournier, Jeremy,Arseniyadis, Stellios,Cossy, Janine
supporting information; experimental part, p. 7562 - 7566 (2012/10/18)
One four all: Allyl dienol carbonates can be readily converted into diversely substituted furans by a one-pot four-step sequence featuring a palladium-catalyzed decarboxylative allylic alkylation, a microwave-mediated Cope rearrangement, a nucleophilic addition, and a dehydration reaction (see scheme). The protocol is operationally simple, highly flexible, and provides di-, tri-, and tetrasubstituted furans starting from readily available materials. Copyright
A synthetic route to α-substituted butenolides: Enantioselective synthesis of (+)-ancepsenolide
Ghobril, Cynthia,Kister, Jeremy,Baati, Rachid
, p. 3416 - 3419 (2011/09/13)
A variety of α-substituted butenolides was efficiently synthesized starting from commercially available tetronic acid and carboxylic acids in four steps. The effectiveness of this approach is illustrated in the short synthesis of one of the first butenoli
