A Stereospecific Route to 6-Substituted 7-Azabicyclo [3.2.1] oct-2-enes.
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918308059531
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3. Rapid chromatographic technique for preparative separations with moderate resolution
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1. 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
2. A novel synthetic route to 6-azabicyclo[3.2.1]oct-3-enes via silicon directed N-Acyliminium chemistry: Synthesis of (±)-gabaculine;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. Selectfluor as a Nucleofuge in the Reactions of Azabicyclo[n.2.1]alkane β-Halocarbamic Acid Esters (n = 2,3);The Journal of Organic Chemistry;2008-02-22
4. Neighboring Group Participation in the Additions of Iodonium and Bromonium Ions to N-Alkoxycarbonyl-2-azabicyclo[2.2.n]alk-5-enes (n = 1,2);The Journal of Organic Chemistry;2008-02-22
5. A Novel Synthesis of 2-Azabicyclo[2.1.1]hexane from Pyridine;The Journal of Organic Chemistry;1998-10-28
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