A New Synthesis of 2-Azabicyclo[2.1.1]hexanes
Author:
Affiliation:
1. Laboratoire de Synthèse Organique, UMR CNRS 6011, Faculté des Sciences, Université du Maine, Avenue Olivier Messiaen, F-72085 Le Mans Cedex 9, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo001790y
Reference41 articles.
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2. Conformational properties of 2,4-methanoproline (2-carboxy-2,4-methanopyrrolidine) in peptides: evidence for 2,4-methanopyrrolidine asymmetry based on solid-state x-ray crystallography, proton NMR in aqueous solution, and CNDO/2 conformational energy calculations
3. 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
4. Synthesis and conformational studies by1H- and13C-nmr spectroscopy of a novel, sterically constrained analogue of thyrotropin-releasing hormone
5. A Concise Route to Novel 1-Aryl and 1-Pyridyl-2-Azabicyclo[2.1.1]hexanes
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