A unified and common intermediate strategy for the asymmetric total synthesis of 3-deoxy-neo-inositol and conduritol E
| dc.contributor.author | Panda A. | en_US |
| dc.contributor.author | Biswas R.G. | en_US |
| dc.contributor.author | Pal S. | en_US |
| dc.date.accessioned | 2025-02-17T05:42:33Z | |
| dc.date.issued | 2016 | |
| dc.description.abstract | A 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. � 2016 | en_US |
| dc.identifier.citation | 3 | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2016.06.127 | |
| dc.identifier.uri | https://idr.iitbbs.ac.in/handle/2008/1160 | |
| dc.language.iso | en | en_US |
| dc.subject | 3-Deoxy-neo-inosotol | en_US |
| dc.subject | Asymmetric synthesis | en_US |
| dc.subject | Carbocycles | en_US |
| dc.subject | Common intermediate | en_US |
| dc.subject | Conduritol E | en_US |
| dc.title | A unified and common intermediate strategy for the asymmetric total synthesis of 3-deoxy-neo-inositol and conduritol E | en_US |
| dc.type | Article | en_US |