1210046-67-5Relevant academic research and scientific papers
Enantioselective carbonyl allylation, crotylation, and tert- prenylation of furan methanols and furfurals via iridium-catalyzed transfer hydrogenation
Bechem, Benjamin,Patman, Ryan L.,Stephen K Hashmi,Krische, Michael J.
supporting information; experimental part, p. 1795 - 1798 (2010/05/01)
Chemical Equation Presentation 5-Substituted-2-furan methanols 1a-c are subject to enantioselective carbonyl allylation, crotylation and tertprenylation upon exposure to allyl acetate, a-methyl allyl acetate, or 1, 1-dimethylallene in the presence of an orthocyclometalated iridium catalyst modified by (R)-Cl,MeOBIPHEP, (R)-C3-TUNEPHOS, and (R)-C3-SEGPHOS, respectively. In the presence of 2-propanol, but under otherwise identical conditions, the corresponding substituted furfurals 2a-c are converted to identical products of allylation, crotylation, and tert-prenylation. Optically enriched products of carbonyl allylation, crotylation, and reverse prenylation 3b, 4b, and 5b were subjected to Achmatowicz rearrangement to furnish the corresponding γ-hydroxy-β-pyrones 6a-c, respectively, with negligible erosion of enantiomeric excess.
