13 C‐NMR‐Spektroskopie: Besondere Hochfeldeffekte in Bicyclo[4.1.1]‐ und Tricyclo[5.1.0.0 2,8 ]octan‐Systemen (1,3‐Cycloheptadien‐Effekt) und besondere Tieffeldeffekte in Dihalogenbicyclo[2.1.1]hex‐2‐enen (Cyclopenten‐Effekt)-Reference-Cited by-同舟云学术

13 C‐NMR‐Spektroskopie: Besondere Hochfeldeffekte in Bicyclo[4.1.1]‐ und Tricyclo[5.1.0.0 2,8 ]octan‐Systemen (1,3‐Cycloheptadien‐Effekt) und besondere Tieffeldeffekte in Dihalogenbicyclo[2.1.1]hex‐2‐enen (Cyclopenten‐Effekt)

Published:1986-10 Issue:10 Volume:119 Page:3067-3075
ISSN:0009-2940
Container-title:Chemische Berichte
language:en
Short-container-title:Chem. Ber.

Author:

Christl Manfred¹,Herzog Clemens¹

Affiliation:

1. Institut für Organische Chemie der Universität Würzburg, Am Hubland, D‐8700 Würzburg

Publisher

Wiley

Subject

Inorganic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19861191014

Reference29 articles.

1. Aus der DissertationC.Herzog Univ. Würzburg1986.

2. NMR‐Untersuchungen an Tricyclo[5.3.0.0 2,8 ]decan‐Systemen – Ungewöhnliche Hochfeldverschiebungen bei sterisch fixierten Cycloheptadien‐Fragmenten

3. Conjugative interaction between .PI. and cyclobutane orbitals. The synthesis and electronic structure of bicyclo[4.1.1]octa-2,4-diene

4. Bicyclo[4.1.1]octa‐2,4‐dien, ‐oct‐2‐en, ‐oct‐3‐en und ‐octan aus Norpinen

5. Tricyclo[5.1.0.02,8]octa-3,5-diene (octavalene)

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