124786-67-0Relevant academic research and scientific papers
Asymmetric intermolecular C-H functionalization of benzyl silyl ethers mediated by chiral auxiliary-based aryldiazoacetates and chiral dirhodium catalysts
Davies, Huw M. L.,Hedley, Simon J.,Bohall, Brooks R.
, p. 10737 - 10742 (2007/10/03)
C-H functionalization of benzyl silyl ethers by means of rhodium-catalyzed insertions of aryldiazoacetates can be achieved in a highly diastereoselective and enantioselective manner by judicious choice of chiral catalyst or auxiliary. The dirhodium tetrap
On the Acylation of Hydroxy- and Mercaptocarboxylic Acid Esters Using the Carbodiimide/Acylation Catalyst Method
Rao, Nagaraj N.,Roth, Hermann J.
, p. 523 - 530 (2007/10/02)
Acylation of esters of hydroxycarboxylic acids can be carried out easily and in good yields by using the carbodiimide/acylation catalyst method.The reaction has also been applied to dihydroxy- and mercaptocarboxylic acid esters.The compounds formed from certain esters of hydroxycarboxylic acids are unstable to heat and decompose easily to free carboxylic acids.Use of racemic carboxylic acids leads to diastereomers, whose (1)H-NMR shifts for characteristic protons are different as expected.Five drugs are among the carboxylic acids investigated in this context.
