60249-12-9Relevant academic research and scientific papers
Palladium-Catalyzed Regioselective and Diastereoselective C-Glycosylation by Allyl-Allyl Coupling
Li, Junhao,Zheng, Nan,Duan, Xuelun,Li, Rui,Song, Wangze
supporting information, p. 846 - 850 (2020/12/13)
A Pd-catalyzed C-glycosylation reaction was developed by allyl-allyl coupling process using Achmatowicz rearrangement products as donors and methylcoumarins as acceptors under mild conditions. This method featured regio- and diastereoselectivities, stereo
Lipase-Induced Oxidative Furan Rearrangements
Blume, Fabian,Sprengart, Petra,Deska, Jan
supporting information, p. 1293 - 1296 (2018/01/27)
Lipase B from Candida antarctica catalyzes the oxidative ring expansion of furfuryl alcohols using aqueous hydrogen peroxide to yield functionalized pyranones under mild conditions. The method further allows for the preparation of corresponding piperidinone derivatives by enzymatic rearrangement of N-protected furfurylamines.
Synthesis of functionalised cyclopentenones via rearrangement of pyranones
Caddick, Stephen,Cheung, Steven,Frost, Lisa M.,Khan, Safraz,Pairaudeau, Garry
, p. 6879 - 6882 (2007/10/03)
Substituted functionalised cyclopentenones could be obtained via base-mediated isomerisation of pyranones. (C) 2000 Elsevier Science Ltd.
PREPARATION OF 6-HYDROXY-2H-PYRAN-3(6H)-ONE FROM 2-FURYLCARBINOL BY PHOTOOXIDATION. SYNTHESIS OF A PHEROMONE OF VESPA ORIENTALIS
Kuo, Yueh-Hsiung,Shih, Kae-Shyang
, p. 1941 - 1949 (2007/10/02)
Photooxidation of 2-furylcarbinols followed by reduction with triphenylphosphine afforded 6-hydroxy-2H-pyran-3(6H)-ones in excellent yield.The method was applied to synthesis of 6-undecyltetrahydro-2-pyrone, a pheromone of Vespa orientalis.
