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Eine Cyanogruppe als Dienophil in einer intramolekularen π4 + π2-Cycloaddition

✍ Scribed by Karl-Heinz Pfoertner; Will E. Oberhänsli


Publisher
John Wiley and Sons
Year
1975
Tongue
German
Weight
655 KB
Volume
58
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

At elevated temperatures the 11, 14‐cycloadducts of tetracyanoethylene with esters of retinoic acid or with retinol acetate are transformed into 5,9‐methano‐2__H__‐cyclohepta[b]‐pyridines by intermolecular ~π~4 + ~π~2‐cycloaddition of a cyano group followed by a double bond shift. The resulting structure was determined by x‐ray analysis.


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