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dc.contributor.authorBabu, K Chandra-
dc.contributor.authorRamadasu, G-
dc.contributor.authorGangaiah, L-
dc.contributor.authorMadhusudhan, G-
dc.contributor.authorMukkanti, K-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.description.abstractA new route for the synthesis of (R)-glyceraldehyde acetonide via asymmetric dihydroxylation of allyl 4-methoxybenzoate using the (DHQ)2PHAL, K2OsO4·2H2O catalyst system is described. This route involves the asymmetric dihydroxylation of allyl 4-methoxybenzoate, acetonide protection of vicinyl dihydroxyl groups followed by cleavage of p-methoxybenzoate ester and subsequent oxidation to give the (R)-glyceraldehyde acetonide.en_US
dc.sourceIJC-B Vol.49B(02) [February 2010]en_US
dc.subject(R)-Glyceraldehyde acetonideen_US
dc.subjectasymmetric dihydro­xy­lationen_US
dc.subjectallyl 4-methoxybenzoateen_US
dc.subjectchiral building blocken_US
dc.subjectSwern oxidationen_US
dc.titleA new route for the synthesis of (R)-glyceraldehyde acetonide: A key chiral building blocken_US
Appears in Collections:IJC-B Vol.49B(02) [February 2010]

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