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ChemInform Abstract: Synthesis of Enantiomerically Pure (+)- and (-)-18-Methoxycoronaridine Hydrochloride and Their Preliminary Assessment as anti-Addictive Agents

2010, ChemInform

ChemInform 1989, 20, No. 44, Abstract 183 ChemInform 1989, 20, No. 44, Abstract 183 ChemInform Abstract Etherification of the butenolides (II) with menthol (I) gives a mixture of the diastereomers (III) and (IV) which are separated by chromatography. Hydrogenation of the butenolides (III) forms the enantiomerically pure γ-lactones (V). (Vb) and (Vc) are reduced to yield the (R)-(+)-and the (S)-(-)-enantiomers of the diol (VI).