Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes

Bredenkötter B, Barth D, Kuck D (1999)
CHEMICAL COMMUNICATIONS (9): 847-848.

Journal Article | Published | English

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Abstract
Strained cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes are accessible in good yield by two-fold cyclodehydration of cis-2,6-diphenylspiro [cyclohexane- 1,2'-indane]-1', 3'-diols and the particularly high acidity of their 'inverted' benzylic bridgehead C-H bonds, causing facile epimerization to the more stable all-cis-tribenzo[5.5.5.6]fenestranes, is shown.
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Bredenkötter B, Barth D, Kuck D. Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes. CHEMICAL COMMUNICATIONS. 1999;(9):847-848.
Bredenkötter, B., Barth, D., & Kuck, D. (1999). Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes. CHEMICAL COMMUNICATIONS(9), 847-848.
Bredenkötter, B., Barth, D., and Kuck, D. (1999). Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes. CHEMICAL COMMUNICATIONS, 847-848.
Bredenkötter, B., Barth, D., & Kuck, D., 1999. Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes. CHEMICAL COMMUNICATIONS, (9), p 847-848.
B. Bredenkötter, D. Barth, and D. Kuck, “Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes”, CHEMICAL COMMUNICATIONS, 1999, pp. 847-848.
Bredenkötter, B., Barth, D., Kuck, D.: Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes. CHEMICAL COMMUNICATIONS. 847-848 (1999).
Bredenkötter, Björn, Barth, Dieter, and Kuck, Dietmar. “Synthesis and base-induced epimerization of cis,cis,cis,trans-tribenzo[5.5.5.6]fenestranes”. CHEMICAL COMMUNICATIONS 9 (1999): 847-848.
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