A new highly diastereoselective synthesis of 2,5-disubstituted-1,3-dioxolan-4-ones from α-hydroxyacids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Enantioselective syntheses of aldols and homoallylic alcohols from 1,3-dioxolan-4-ones using mandelic acid as chiral auxiliary
2. Optically active 2-ethenyl-1,3-dioxolanones as 3-carbon synthons. Allylnickel derivatives as homoenolate equivalents
3. Synthesis of enantiomerically enriched atrolactic acid and other α-hydroxy acids
4. Chirality transfer from lactic acid selective synthesis of 2,2-disubstituted-1,3-dioxolan-4-ones from ketones and acetals
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