Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues
Reference:
Riley, A. M., Godage, H. Y., Mahon, M. F. and Potter, B. V. L., 2006. Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate gives rapid access to precursors for second messenger analogues. Tetrahedron: Asymmetry, 17 (2), pp. 171-174.
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Abstract
Chiral desymmetrisation of myo-inositol 1,3,5-orthobenzoate via the formation of diastereoisomeric bis[(1S)-(-)-camphanate] esters provides a convenient and fast route to precursors for biologically important inositol phosphates and lipids, and to synthetic analogues and probes modified at O-1 or O-3 of the inositol ring. (c) 2005 Elsevier Ltd. All rights reserved.
Details
| Item Type | Articles |
| Creators | Riley, A. M., Godage, H. Y., Mahon, M. F. and Potter, B. V. L. |
| DOI | 10.1016/j.tetasy.2005.12.008 |
| Departments | Faculty of Science > Chemistry |
| Refereed | Yes |
| Status | Published |
| ID Code | 4666 |
| Additional Information | ID number: ISI:000235579500002 |
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