Dysidazirine

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

<ol>
<li id="fn:1"><p>"Despite my high ring strain, I'm pretty stable. What molecule am I?". ACS.org. American Chemical Society. Retrieved 18 November 2022. <a href="https://www.acs.org/content/acs/en/molecule-of-the-week/archive/d/r-dysidazirine.html" target="_blank">https://www.acs.org/content/acs/en/molecule-of-the-week/archive/d/r-dysidazirine.html</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li>
<li id="fn:2"><p>Davis, Franklin A.; Reddy, G. Venkat; Liu, Hu (1995). "Asymmetric Synthesis of 2H-Azirines: First Enantioselective Synthesis of the Cytotoxic Antibiotic (R)-(-)-Dysidazirine". Journal of the American Chemical Society. 117 (12): 3651–3652. doi:10.1021/ja00117a050. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li>
<li id="fn:3"><p>Skepper, Colin K.; Dalisay, Doralyn S.; Molinski, Tadeusz F. (2008). "Synthesis and Antifungal Activity of (−)-(Z)-Dysidazirine". Organic Letters. 10 (22): 5269–5271. doi:10.1021/ol802065d. PMC 2635126. PMID 18937483. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635126" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2635126</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li>
<li id="fn:4"><p>"Despite my high ring strain, I'm pretty stable. What molecule am I?". ACS.org. American Chemical Society. Retrieved 18 November 2022. <a href="https://www.acs.org/content/acs/en/molecule-of-the-week/archive/d/r-dysidazirine.html" target="_blank">https://www.acs.org/content/acs/en/molecule-of-the-week/archive/d/r-dysidazirine.html</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li>
</ol>

Dysidazirine open-in-new

Dysidazirine