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Preparation of chiral annulated indenes derived from nopinone, verbenone and menthone

✍ Scribed by Ronald L. Halterman; Lisa D. Crow


Book ID
104253294
Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
148 KB
Volume
44
Category
Article
ISSN
0040-4039

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✦ Synopsis


A three-step procedure for the synthesis of chiral annulated indenes is described in which nopinone, verbenone and menthone are converted to their enolate form, alkylated with 2-bromomethylbromobenzene, ring-closed with CrCl 2 /cat. NiCl 2 and dehydrated with catalytic acid.


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