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Title: Convenient synthesis of D- and L-xylo-1,2,3,4-alkane tetrols from a D-gluco-configured common building block. Author: Borkar SR, Manjunath BN, Balasubramaniam S, Aidhen IS. Journal: Carbohydr Res; 2012 Sep 01; 358():23-30. PubMed ID: 22863364. Abstract: D-gluco-configured building block derived from D-(+)-gluconolactone has served as a common chiral template for the synthesis of enantiopure D- and L-xylo-configured 1,2,3,4-alkane tetrols. This has enabled synthesis of medicinally important guggultetrols and their enantiomers from a common starting point. Wittig and Grignard reactions are the key steps used for the incorporation of lipophilic chain.[Abstract] [Full Text] [Related] [New Search]