TY  - JOUR
AU  - Rodríguez, C.M.
AU  - Ravelo, J.L.
AU  - Martín, V.S.
T1  - γ-Lactone-tethered ring-closing metathesis. A route to enantiomerically enriched γ-lactones α,β-fused to medium-sized rings
LA  - eng
PY  - 2004
SP  - 4787
EP  - 4789
T2  - Organic Letters
SN  - 1523-7060
VL  - 6
IS  - 25
AB  - (Chemical Equation Presented) The stereoselective alkylation of α(phenylsulfonyl)-β-[(methoxycarbonyl)methyl]-γ-lactones obtained by the base-induced cyclization of enantiomericaily enriched α-[(phenylthio)acyl]-α,β-unsaturated esters and ring-closing olefin metathesis (RCM) are the basis of a new approach for gaining access to γ-lactones that are α,β-fused to medium-sized carbocycles and cyclic ethers.
DO  - 10.1021/OL0478739
UR  - https://portalciencia.ull.es/documentos/5e3adcee299952629a024b6f
DP  - Dialnet - Portal de la Investigación
ER  -