38115-87-6Relevant articles and documents
Catalytic oxidative decarboxylation of malic acid into dimethyl malonate in methanol with dioxygen
Liu, Junxia,Du, Zhongtian,Yang, Yanliang,Lu, Tianliang,Lu, Fang,Xu, Jie
, p. 2151 - 2154 (2013/01/15)
If you've got it, use it: Malic acid is converted into dimethyl malonate by a direct, one-pot process. The process is cyanide- and halide-free. Phosphovanadomolybdates serve as bifunctional catalysts, effecting the oxidative decarboxylation and esterification in a consecutive manner. Oxidative C-C bond cleavage first forms hemiacetals. The results serve as example for the production of valuable chemicals by fully utilizing the oxygen atoms and basic structure inherent to biomass products.
A NEW CHIRAL HOST COMPOUND 10,10'-DIHYDROXY-9,9'-BIPHENANTHRYL. OPTICAL RESOLUTION OF PROPIONIC ACID DERIVATIVES, BUTYRIC ACID DERIVATIVES, AND 4-HYDROXYCYCLOPENT-2-EN-1-ONE DERIVATIVES BY COMPLEXATION
Toda, Fumio,Tanaka, Koichi
, p. 1807 - 1810 (2007/10/02)
Optically active 10,10'-dihydroxy-9,9'-biphenanthryl was designed as a new chiral host compound for optical resolution of guest compounds, and was found to be wery effective for resolution of the title guest compounds.