Prasad, Kavirayani R. ; Anbarasan, Pazhamalai (2006) Enantiodivergent synthesis of both antipodes of hydroxy-exo-brevicomin from L-(+)-tartaric acid Tetrahedron Letters, 62 (35). pp. 8303-8308. ISSN 0040-4039
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2006.06.053
Abstract
An enantiodivergent approach to both antipodes of hydroxy-exo-brevicomin was achieved from a common chiral precursor L-(+)-tartaric acid. The strategy utilizes the elaboration of a keto-Weinreb amide and successive stereoselective reductions.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Stereoselective Reduction; l-(+)-Tartaric Acid; Hydroxy-exo-brevicomin; 6,8-Dioxabicyclo[3.2.1]octane |
| ID Code: | 105840 |
| Deposited On: | 21 Dec 2017 12:05 |
| Last Modified: | 21 Dec 2017 12:05 |
Repository Staff Only: item control page
