66633-36-1Relevant academic research and scientific papers
FACILE PREPARATION OF 2,6-DIMETHYL-2,6-TETRAHYDROPYRANCARBOLACTONE, A VERSATILE INTERMEDIATE FOR THE SYNTHESES OF (+/-)-FRONTALIN, (+/-)-CINENIC ACID, AND (+/-)-LINALOYL OXIDE
Utaka, Masanori,Makino, Hiroshi,Oota, Yukito,Tsuboi, Sadao,Takeda, Akira
, p. 2567 - 2570 (2007/10/02)
2,6-Dimethylcyclohexanone has been converted via its 2,6-dihydroxy derivative by base-catalyzed oxygenation to 2,6-dimethyl-2,6-tetrahydropyrancarbolactone which can be used as a key intermediate for the syntheses of the title natural products in racemic forms.
Electrooxidative Cleavage of Carbon-Carbon Linkages. 1. Preparation of Acylic Oxoalkanoates from 2-Hydroxy- and 2-Acetoxy-1-cycloalkanones and Cycloalkanone Enol Acetates
Torii, Sigeru,Inokuchi, Tsutomu,Oi, Ryu
, p. 47 - 52 (2007/10/02)
A methodology is described for the synthesis of acyclic oxoalkanoates 2 by electrooxidative cleavage of carbon-carbon linkages of 2-oxocycloalkan-1-ols 1 and cycloalkanone enol acetates 3.The electrolysis of 1 was carried out in a MeOH-LiClO4-(Pt) system at a constant applied voltage of 20 V by using a divided cell, giving 2 in 82-97 percent yields.On the other hand, 3 was electrolyzed in MeOH-AcOH (10:1)-LiClO4-(Pt) at 2-8 deg to give 2 in 72-79 percent yields.Electrolysis of 4-hydroxy-p-menth-8-ene afforded methyl (3R)-3,7-dimethyl-6-oxo-7-octenoate, a chiral synthetic block for the synthesis of (+)-rose oxide, in 84 percent yield.Similarly, the procedure could be applied to the preparation of methyl(+)-6-oxo-6,7-dihydrocitronellate from (+)-menthone enol acetate (74 percent) as well as 4-hydroxy-p-menthone (94 percent).Other lithium salts, i.e., LiBF4 and CF3CO2Li, can be used for the present purpose, but there are some difficulties in producing 2 with Et4NOTs and Et4NClO4.A plausible mechanism of the formation of 2 from 1 is also discussed.
