Cation induced rearrangement of 8-azabicyclo[3.2.1]octa-2,6-dienes to 6-azabicyclo[3.2.1]oct-2-enes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference27 articles.
1. Synthesis of (.+-.)-ferruginine and (.+-.)-anhydroecgonine methyl-ester by a tandem cyclopropanation/Cope rearrangement
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3. Synthesis of 2.beta.-Acyl-3.beta.-aryl-8-azabicyclo[3.2.1]octanes and Their Binding Affinities at Dopamine and Serotonin Transport Sites in Rat Striatum and Frontal Cortex
4. Synthesis of 3β-Aryl-8-azabicyclo[3.2.1]octanes with High Binding Affinities and Selectivities for the Serotonin Transporter Site
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1. Methods and Strategies for the Synthesis of Peduncularine;Chinese Journal of Organic Chemistry;2019
2. Stereoselective Synthesis of 7-(E )-Arylidene-2-chloro-6-azabicyclo[3.2.1]octanes via Aluminum Chloride-Promoted Cyclization/Chlorination of Six-Membered Ring 3-Enynamides;Advanced Synthesis & Catalysis;2017-04-28
3. Carbamoyl Radical‐Mediated Synthesis and Semipinacol Rearrangement of β‐Lactam Diols;Chemistry – A European Journal;2014-04-07
4. ChemInform Abstract: Cation Induced Rearrangement of 8-Azabicyclo[3.2.1]octa-2,6-dienes to 6-Azabicyclo[3.2.1]oct-2-enes.;ChemInform;2010-06-19
5. Epoxide Opening-Induced Tandem 8-Azabicyclo[3.2.1]octane to 6-Azabicyclo[3.2.1]octane Rearrangement−Iminium Allylation: Synthesis of (±)-Peduncularine;Organic Letters;2010-05-14
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