Formation of keto-carbeniums from 1,2,2-triarylacenaphthen-1-ols by breaking a long CC bond: unusual alcohol protonolysis accompanied by formal hydride abstraction-Reference-Cited by-同舟云学术

Formation of keto-carbeniums from 1,2,2-triarylacenaphthen-1-ols by breaking a long CC bond: unusual alcohol protonolysis accompanied by formal hydride abstraction

Published:2003-08 Issue:32 Volume:44 Page:6095-6098
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Suzuki Takanori,Nagasu Takayuki,Kawai Hidetoshi,Fujiwara Kenshu,Tsuji Takashi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. 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

2. The Nature of the Long Bond in 3,8-Dichloro-1,1,2,2-tetraphenylcyclobuta[b]naphthene

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

4. Tetraphenyldihydrocyclobutaarenes—what causes the extremely long 1.72 Å C–C single bond?

5. Does π−σ−π Through-Bond Coupling Significantly Increase C−C Bond Lengths?

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