940000-68-0Relevant academic research and scientific papers
Hydroxyl group deprotection reactions with Pd(OH)2/C: a convenient alternative to hydrogenolysis of benzyl ethers and acid hydrolysis of ketals
Murali, Chebrolu,Shashidhar, Mysore S.,Gopinath, Chinnakonda S.
, p. 4149 - 4155 (2007)
Benzyl ethers, ketals and orthoformates were cleaved with Pd(OH)2/C in methanol, to generate the corresponding alcohol; carboxylic acid esters were stable under these reaction conditions. Pd(OH)2/C in methanol was used for the deprotection of hydroxyl groups during the preparation of sequoyitol via myo-inositol orthobenzoate. This method of deprotection has the potential to be useful in the synthesis of different classes of organic compounds since the reaction conditions do not involve strong acids, bases or hydrogen.
Thermal epimerization of inositol 1,3-benzylidene acetals in the molten state
Gurale, Bharat P.,Krishnaswamy, Shobhana,Vanka, Kumar,Shashidhar, Mysore S.
, p. 7280 - 7288 (2011/10/08)
1,3-O-Benzylidene-2,4,5,6-tetra-O-substituted-myo-inositol derivatives obtained by the DIBAL-H reduction of the corresponding myo-inositol 1,3,5-orthobenzoate derivatives undergo epimerization at the acetal carbon on heating, in the molten state, just abo
