51019-55-7Relevant articles and documents
Clicked AC regioisomer cationic cyclodextrins for enantioseparation
Zhou, Jie,Liu, Yun,Lu, Yingying,Tang, Jian,Tang, Weihua
, p. 54512 - 54516 (2015/02/05)
Novel AC regioisomer cationic cyclodextrins have been successfully prepared with azide/alkyne click chemistry. The clicked CDs were explored for the enantioseparation of acidic racemates in capillary electrophoresis.
Iodide-catalyzed reductions: Development of a synthesis of phenylacetic acids
Milne, Jacqueline E.,Storz, Thomas,Colyer, John T.,Thiel, Oliver R.,Dilmeghani Seran, Mina,Larsen, Robert D.,Murry, Jerry A.
experimental part, p. 9519 - 9524 (2012/01/06)
A new convenient and scalable synthesis of phenylacetic acids has been developed via the iodide catalyzed reduction of mandelic acids. The procedure relies on in situ generation of hydroiodic acid from catalytic sodium iodide, employing phosphorus acid as the stoichiometric reductant.
Regioselective alkylation of lithium dienediolates of α,β- unsaturated carboxylic acids
Brun, Eva M.,Gil, Salvador,Mestres, Ramón,Parra, Margarita
, p. 1160 - 1165 (2007/10/03)
Lithium carboxylic acids dienediolates are regioselectively alkylated at the α-carbon by reaction with tosylates derived from both primary and secondary alcohols. Both regio- and diastereoselectivity are improved when compared with those obtained in the c