Second-Chance Rearrangement Route to Novel 5(6)-Syn,anti-difunctional 2-Azabicyclo[2.1.1]hexanes
Author:
Affiliation:
1. Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0349662
Reference17 articles.
1. The Rearrangement Route to 3-CH2X-2-azabicyclo[2.1.1]hexanes. Substituent Control of Neighboring Group Participation
2. A Novel Synthesis of 2-Azabicyclo[2.1.1]hexane from Pyridine
3. Synthesis of Novel 2-Azabicyclo[2.2.0]- and [2.1.1]hexanols
4. Conformational Stability of Collagen Relies on a Stereoelectronic Effect
5. Conformational properties of 2,4-methanoproline (2-carboxy-2,4-methanopyrrolidine) in peptides: determination of preferred peptide bond conformation in aqueous solution by proton Overhauser measurements
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