NMR Studies of Hindered Rotation and Magnetic Anisotropy: The Diels–Alder Adducts of Phencyclone withN‐Phenylmaleimide andN‐(2‐Trifluoromethylphenyl)maleimide. Ab Initio Calculations for Optimized Structures-Reference-Cited by-同舟云学术

NMR Studies of Hindered Rotation and Magnetic Anisotropy: The Diels–Alder Adducts of Phencyclone withN‐Phenylmaleimide andN‐(2‐Trifluoromethylphenyl)maleimide. Ab Initio Calculations for Optimized Structures

Published:2004-12-31 Issue:5 Volume:37 Page:469-492
ISSN:0038-7010
Container-title:Spectroscopy Letters
language:en
Short-container-title:Spectroscopy Letters

Author:

Marshall Kimberly,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-120039703

Reference18 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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