Iridoids. Asymmetric Synthesis Via Enantiomeric Separation of the Mono Methylester of 2, 3‐DI‐Endo‐Hydroxycarbonyl‐5‐Norbornene
- 1 January 1984
- journal article
- research article
- Published by Wiley in Bulletin des Sociétés Chimiques Belges
- Vol. 93 (11), 999-1004
- https://doi.org/10.1002/bscb.19840931110
Abstract
Enantiomeric separation of racemic mono methylester of the known 2, 3‐di‐endo‐hydroxycarbonyl‐5‐norbornene (2) is possible via the ephedrine salts. Both enantiomers can be converted into 2, R‐endo‐methoxycarbonyl‐3, S‐endo‐hydroxymethyl‐5‐norbornene (−)−4, which is a suitable intermediate for asymmetric synthesis of iridoids.This publication has 8 references indexed in Scilit:
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