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-Reference-Cited by-同舟云学术

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

Published:2005-07 Issue:5 Volume:42 Page:889-898
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Callahan Ronald,Ramirez Orlando,Rosmarion Kerstin,Rothchild Robert,Bynum Kevin C.

Publisher

Wiley

Subject

Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570420522/fullpdf

Reference30 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

5. NMR Studies of Hindered Rotation. The Diels-Alder Adduct of 4-Methyl-1, 2, 4-triazoline-3, 5-dione with Phencyclone: Restricted Motion of Unsubstituted Bridgehead Phenyls.

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