59516-90-4Relevant academic research and scientific papers
Iron-Catalyzed Arene Prenylation
Villani-Gale, Alexander J.,Eichman, Chad C.
supporting information, p. 2925 - 2928 (2016/07/11)
The syntheses of prenylated arenes and 2,2-dimethylchromans using a Friedel–Crafts-type coupling between activated arenes and isoprene is reported. A combination of catalytic amounts of FeCl3and AgBF4promotes a regioselective prenyla
InIII-catalysed tandem C-C and C-O bond formation between phenols and allylic acetates
Vece, Vito,Ricci, Jeremy,Poulain-Martini, Sophie,Nava, Paola,Carissan, Yannick,Humbel, Stephane,Dunach, Elisabet
supporting information; experimental part, p. 6239 - 6248 (2010/12/29)
Indium triflate catalysed tandem allylation-intramolecular hydroalkoxylation was efficiently carried out by using 1 mol-% of the catalyst under mild conditions to afford the dihydrobenzopyran ring system (chroman-type structure) in good yields. Kinetic, mechanistic and theoretical studies are also presented. Tandem allylation-intramolecular hydroalkoxylation carried out in the presence of an indium catalyst (1 mol-%) under mild conditions provides the dihydrobenzopyranring system in good yields. Kinetic, mechanistic and theoretical studies are presented.
Fragrance compositions of alicyclic ketone and alcohol derivatives
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, (2008/06/13)
Alicyclic ketone and alcohol derivatives having the structure: STR1 wherein the dotted line represents a carbon-carbon double bond or a carbon-carbon single bond; wherein Z is STR2 and wherein each of R1, R2, R3, R4, and R5 is hydrogen or lower alkyl are useful as odor-modifying ingredients in perfumes and perfumed products and as flavor-modifying ingredients in foodstuffs and tobacco products. These derivatives may be prepared from substituted phenols having the structure: STR3
