Proton and Carbon‐13 NMR Studies of the Phencyclone Adducts of Medium Alkyl Chain‐LengthN‐n‐Alkylmaleimides. Hindered Rotations and Magnetic Anisotropic Effects. Ab initio Calculations for Optimized Structures-Reference-Cited by-同舟云学术

Proton and Carbon‐13 NMR Studies of the Phencyclone Adducts of Medium Alkyl Chain‐LengthN‐n‐Alkylmaleimides. Hindered Rotations and Magnetic Anisotropic Effects. Ab initio Calculations for Optimized Structures

Published:2004-12-31 Issue:5 Volume:37 Page:493-516
ISSN:0038-7010
Container-title:Spectroscopy Letters
language:en
Short-container-title:Spectroscopy Letters

Author:

Sklyut Olga,Prip Ron,Azar Nikolay,Callahan Ronald,Rothchild Robert

Publisher

Informa UK Limited

Subject

Spectroscopy,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1081/SL-120039699

Reference27 articles.

1. Molecular design by cycloaddition reactions. XXV. High peri- and regiospecificity of phencyclone

2. Synthesis of Diels?Alder Adducts of Phencyclone and NMR Studies of Hindered Rotations of Unsubstituted Bridgehead Phenyls: Microscale Experiments in Organic Chemistry

3. NMR Studies of Hindered Rotation. The Diels-Alder Adduct of Phencyclone withN-n-Propylmaleimide: Restricted Motion of Bridgehead Phenyls

4. NMR Studies of Hindered Rotation. The Diels-Alder Adduct of N-n-Butylmaleimide With Phencyclone: Restricted Motion of Bridgehead Phenyls

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5. Multinuclear NMR studies andab initiostructure calculations of hindered phencyclone diels-alder adducts from symmetrical cyclic dienophiles: Cyclohexene, vinylene carbonate, vinylene trithiocarbonate and twoN-aryl maleimides;Journal of Heterocyclic Chemistry;2005-07