@misc{10498/20582,
year = {2015},
url = {http://hdl.handle.net/10498/20582},
abstract = {Solvent-free desymmetrisation of a meso-dialdehyde with chiral alcohols, led to preparation of 4- silyloxy-6-alkyloxytetrahydro-2H-pyran-2-one derivatives with a 96% de. This methodology, which yields the corresponding methyl nor-mevaldates with 99% ee, has been applied to the enantioselective synthesis of the ( )-(R) and (þ)-(S) nor-mevalonic acid lactones.},
publisher = {Elsevier},
keywords = {Botrytis cinerea},
keywords = {Desymmetrisation},
keywords = {meso-Dialdehyde},
keywords = {Nor-methyl mevaldate},
title = {Diastereoselective and enantioselective preparation of nor-mevaldic acid surrogates through desymmetrisation methodology. Enantioselective synthesis of (+) and (-) nor-mevalonic lactones},
doi = {10.1016/j.tet.2015.08.010},
author = {Botubol Ares, José Manuel and Durán Peña, María Jesús and Hernández Galán, Rosario and González Collado, Isidro and M. Harwood, Laurence and Macías Sánchez, Antonio José},
}