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3-Phenylisochromane aus 1-Benzylisochinolinen durch Bromcyan-Abbau

URN to cite this document:
urn:nbn:de:bvb:355-epub-155147
Prior, S. ; Wiegrebe, Wolfgang
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Date of publication of this fulltext: 22 Jun 2010 09:58


Abstract

Die Umsetzung von Laudanosin-6'-carbonsäure (1c) mit BrCN führt zu dem Phenylisochromanon
3b; aus 6'-Hydroxymethyllaudanosin (1b) entsteht das Phenylisochroman 3a.

Reaction of laudanosine-6'-carboxylic acid (1c) with BrCN leads to the phenylisochromanone 3b; the
phenylisochroman 3a arises from 6'-hydroxymethyl-laudanosine (1b).


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