From (−)-quinic acid to 8-azabicyclo[3.2.1]octane framework: Preparation of an enantiopure tropan-6α-ol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. (−)-Quinic acid: configurational (stereochemical) descriptors
2. D-(−)-Quinic acid: a chiron store for natural product synthesis
3. A unified asymmetric approach to substituted hexahydroazepine and 7-azabicyclo[2.2.1]heptane ring systems from D(−)-quinic acid: Application to the formal synthesis of (−)-balanol and (−)-epibatidine
4. Enantioselective formal synthesis of (−)-ovalicin using quinic acid as a chiral template
5. Enantioselective approach to 7-azabicyclo[2.2.1]heptane ring systems using D-(−)-quinic acid as the chiral educt: Application to the formal synthesis of (+)-epibatidine
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1. Enantioselective Synthesis of Tropanes: Brønsted Acid Catalyzed Pseudotransannular Desymmetrization;Angewandte Chemie;2020-04-20
2. Enantioselective Synthesis of Tropanes: Brønsted Acid Catalyzed Pseudotransannular Desymmetrization;Angewandte Chemie International Edition;2020-03-05
3. The Chemical Synthesis and Applications of Tropane Alkaloids;The Alkaloids: Chemistry and Biology;2019
4. Desymmetrization of meso-Dibromocycloalkenes through Copper(I)-Catalyzed Asymmetric Allylic Substitution with Organolithium Reagents;Journal of the American Chemical Society;2018-05-23
5. The Krapcho Dealkoxycarbonylation Reaction of Esters with α-Electron-Withdrawing Substituents;Organic Reactions;2013-05-30
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