Stibole

<h2 id="reactions">Reactions</h2>
<p>2,5-Dimethyl-1-phenyl-1<i>H</i>-stibole, for example, can be formed by the reaction of 1,1-dibutyl-2,5-dimethyl<a href="/facts/Stannole/f185mtqp">stannole</a> and dichlorophenylstibine.<a class="footnote-ref" id="fnref:1" href="#fn:1"><sup>1</sup></a> Stiboles can be used to form <a href="/facts/Ferrocene/jKtu9Cp8">ferrocene</a>-like <a href="/facts/Sandwich_compound/uhupMGDU">sandwich compounds</a>.<a class="footnote-ref" id="fnref:2" href="#fn:2"><sup>2</sup></a>
</p>
<h2 id="see-also">See also</h2>
<ul><li><a href="/facts/Organoantimony_chemistry/96Y0TNlp">Organoantimony chemistry</a></li></ul>

<h2 id="references">References</h2>

<ol>
<li id="fn:1"><p>J.I.G. Cadogan; S.V. Ley; G. Pattenden; R.A. Raphael; C.W. Rees, eds. (1996), Dictionary of Organic Compounds, vol. 3 (6 ed.), Chapman & Hall, p. 2710, ISBN 978-0-412-54090-5, retrieved 2010-03-04 <a href="978-0-412-54090-5" target="_blank">978-0-412-54090-5</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li>
<li id="fn:2"><p>A.R. Katritzky; Otto Meth-Cohn; C.W. Rees, eds. (1995), Comprehensive Organic Functional Group Transformations, vol. 4, Elsevier, pp. 1038–1040, ISBN 978-0-08-042325-8, retrieved 2010-03-04 <a href="978-0-08-042325-8" target="_blank">978-0-08-042325-8</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li>
</ol>

Stibole open-in-new

Stibole