Panda A.Biswas R.G.Pal S.2025-02-1720163http://dx.doi.org/10.1016/j.tetlet.2016.06.127https://idr.iitbbs.ac.in/handle/2008/1160A competent, simplistic, and unified synthetic approach has been outlined for enantiomerically pure 3-deoxy-neo-inositol and conduritol E starting from D-ribose via a common chiral cyclohexenol derivative. The focal attributes of the synthetic route include stereoselective Grignard reaction, Wittig olefination, ring closing metathesis (RCM), and cis dihydroxylation. � 2016en3-Deoxy-neo-inosotolAsymmetric synthesisCarbocyclesCommon intermediateConduritol EArticle