3‐O‐Methl‐6‐desoxy‐L‐talose, Synthese und Identifizierung mit L‐Acovenose. Desoxyzucker, 43. Mitteilung

Abstract 3‐O‐methly‐6‐deoxy‐ L ‐talose has been synthesized starting from 1, 2–5, 6‐di‐O‐isopropylidene‐α‐ D ‐allose ( 1 ). Methylation, selective acidic hydrolysis, sodium periodate oxidation and G RIGNARD reaction with CH 3 MgBr gave a mixture of the 1, 2‐isopropylidene derivatives of 3‐O‐methyl‐6‐deoxy‐ D ‐allose and 3‐O‐methyl‐6‐deoxy‐ D ‐allose ( 7 ) and 3‐O‐methyl‐6‐deoxy‐ L ‐talose ( 8 ) ( L ‐acovenose) could be obtained. Oxidation of the latter gave the corresponding crystalline lactone, which could be indentified with a sample obtained from natural L ‐acovenose.