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Photocyclodimerization of 5-Methyl-2H-pyran-3(6H)-one

✍ Scribed by Ljubov Groesch; Jürgen Kopf; Paul Margaretha


Publisher
John Wiley and Sons
Year
2008
Tongue
German
Weight
165 KB
Volume
91
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The structures of the main products resulting from photocyclodimerization of the title compound 2 and of other 3‐methyl‐substituted ‘oxacyclohex‐2‐en‐1‐ones’ (=dihydropyranones) were determined by X‐ray crystallography. In connection, the ^13^C‐NMR chemical shifts of the cyclobutane C‐atoms of these dimers allow a clear differentiation between head‐to‐head and head‐to‐tail regioisomers, all structurally related to those of isophorone (1).


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