Lewis Acid Catalyzed Intramolecular Condensation of Ynol Ether-Acetals. Synthesis of Alkoxycycloalkene Carboxylates
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, California State University, Northridge 18111 Nordhoff Street, Northridge, California 91330, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol303026v
Reference30 articles.
1. Copper(I) mediated highly diastereoselective conjugate addition of Grignard reagents to functionalised cycloalkenols: a general and efficient route for the stereoselective synthesis of 5- and 6-membered ring trisubstituted cycloalkanols
2. Alkylation d'acetates de cyclenols fonctionnels (5 et 6 chainons) par les reactifs de grignard et les enolates lithiens catalysee (ou non) par les sels de cuivre (I). Synthese rapide de la (±) mitsugashiwalactone
3. Substitution nucleophile d'acetates de cyclenols allyliques fonctionnels par des organometalliques en presence de sels cuivreux. Application a une synthese rapide de la (±)mitsugashiw alactone
4. Esters α-méthyléniques et α-hydroxyméthylés par addition d'organolithiens ou magnésiens sur l' α-(hydroxymethyl) acrylate d'éthyle et ses dérivés en présence de cuivre(I)
5. Copper(I) mediated highly diastereoselective conjugate addition of grignard reagents to 2-silyloxycyclopentenecarboxylates
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