Nonplanar Structures of Thioamides Derived from 7-Azabicyclo[2.2.1]heptane. Electronically Tunable Planarity of Thioamides-Reference-Cited by-同舟云学术

Nonplanar Structures of Thioamides Derived from 7-Azabicyclo[2.2.1]heptane. Electronically Tunable Planarity of Thioamides

Published:2008-10-24 Issue:22 Volume:73 Page:9102-9108
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hori Tetsuharu¹,Otani Yuko¹,Kawahata Masatoshi¹,Yamaguchi Kentaro¹,Ohwada Tomohiko¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan, and Department of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University, 1314-1 Shido, Sanuki, Kagawa 769-2193, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801996b

Reference30 articles.

1. Barriers to internal rotation in thioamides. Experimental results and molecular orbital calculations

2. Studies of chemical exchange by nuclear magnetic resonance. VI. Comparison of carbon-nitrogen rotational barriers in amides, thioamides, and amidinium ions

3. Why Does Thioformamide Have a Larger Rotational Barrier Than Formamide?

4. Role of Conjugation in the Stabilities and Rotational Barriers of Formamide and Thioformamide. An ab Initio Valence-Bond Study

5. For a counter-example to the resonance effect, see:

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