Extremely Long C−C Bond in (−)-trans-1,2-Di-tert-butyl-1,2-diphenyl- and 1,1-Di-tert-butyl-2,2-diphenyl-3,8-dichlorocyclobuta[b]naphthalenes-Reference-Cited by-同舟云学术

Extremely Long C−C Bond in (−)-trans-1,2-Di-tert-butyl-1,2-diphenyl- and 1,1-Di-tert-butyl-2,2-diphenyl-3,8-dichlorocyclobuta[b]naphthalenes

Published:1999-04-01 Issue:9 Volume:64 Page:3102-3105
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Toda Fumio¹,Tanaka Koichi¹,Watanabe Masaki¹,Tamura Kenichi¹,Miyahara Ikuko¹,Nakai Tadashi¹,Hirotsu Ken¹

Affiliation:

1. Department of Applied Chemistry, Faculty of Engineering, Ehime University, Matsuyama 790-8577, Japan, and Department of Chemistry, Faculty of Science, Osaka City University, Sugimoto-cho, Sumiyoshi-ku, Osaka 950, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo982010c

Reference14 articles.

1. A New Synthetic Route to 1,2-Dihydrocyclobutaarenes

2. Overlong CC Single Bonds

3. [2+2] Cycloaddition Products of Tetradehydrodianthracene: Experimental and Theoretical Proof of Extraordinary Long CC Single Bonds

4. Consistencies between experiments and quantum calculations of strained C–C single bond lengths

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