SN1-like Reactions of Bicyclic α-Amino Ethers with Sulfur, Nitrogen, and Carbon Nucleophiles. Synthesis of 1-Azabicyclo[3.2.2]nonanes Functionalized at Carbon C2 and C6 with Complete Stereocontrol-Reference-Cited by-同舟云学术

SN1-like Reactions of Bicyclic α-Amino Ethers with Sulfur, Nitrogen, and Carbon Nucleophiles. Synthesis of 1-Azabicyclo[3.2.2]nonanes Functionalized at Carbon C2 and C6 with Complete Stereocontrol

Published:2002-09-01 Issue:19 Volume:4 Page:3179-3182
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Röper Stefanie¹,Wartchow Rudolf¹,Hoffmann H. Martin R.¹

Affiliation:

1. Department of Organic Chemistry, University of Hannover, Schneiderberg 1B, D-30167 Hannover, Germany, and Department of Inorganic Chemistry, University of Hannover, Callinstr. 9, D-30167 Hannover, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol026342m

Reference22 articles.

1. Nomofungin: A New Microfilament Disrupting Agent

2. Experimental and theoretical study of excimer formation in 1-azabicyclo[l.m.n]alkanes: interpretation of binding energies using a 3-electron-bond model

3. Intramolecular Schmidt reactions of azides with carbocations: synthesis of bridged-bicyclic and fused-bicyclic tertiary amines

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