Die Ableitung der Stereochemie von 1-Isopropyl-4-methyl-bicyclo[3.1.0]hexan (cis-undtrans-Thujan) durch Protonenresonanz-Spektroskopie
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference23 articles.
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2. Terpenses. I. The Absolute Configuration of (-)-Umbellulone and the Thujane Terpenes
3. The Absolute Configuration of the Thujane Group.
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1. Non-empirical calculations of NMR indirect carbon-carbon coupling constants. Part 5: Bridged bicycloalkanes;Magnetic Resonance in Chemistry;2003
2. The conformations of bicyclo[3.1.0]hexane derivatives by1H and13C NMR;Organic Magnetic Resonance;1981-04
3. Crystal and molecular structure of the N,N-dimethylurea derivatives of exo-5-ethoxy-5-isocyanatobicyclo[2.1.0]pentane and exo-6-ethoxy-6-isocyanatobicyclo[3.1.0]hexane. Confirmation of the .gamma.-steric shift in nitrogen-15 nuclear magnetic resonance as a tool for stereochemical assignment;Journal of the American Chemical Society;1978-08
4. A conformational study of bicyclo[3.1.0] hexane and of the 3-bicyclo[3.1.0]hexyl carbonium ion: an AB initio SCF investigation;Chemical Physics;1978-03
5. Microwave spectrum and conformation of 6-thiabicyclo[3.1.0]hexane;Journal of Molecular Spectroscopy;1976-03
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