An Enantioselective Approach to 4-Substituted Proline Scaffolds: Synthesis of (<i>S</i>)-5-(<i>tert</i>-Butoxy carbonyl)-5-azaspiro[2.4]heptane-6-carboxylic Acid

A catalytic and enantioselective preparation of the (<i>S</i>)-4-methyleneproline scaffold is described. The key reaction is a one-pot double allylic alkylation of an imine analogue of glycine in the presence of a chinchonidine-derived catalyst under phase transfer conditions. These 4-me...

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Bibliographic Details
Main Authors: Blanca López, Martí Bartra, Ramon Berenguer, Xavier Ariza, Jordi Garcia, Roberto Gómez, Hèctor Torralvo
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/25/23/5644