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New synthetic method for orsellic acid type macrolides by intramolecular alkylation of protected cyanohydrin. The synthesis of (±)-zearalenone.

✍ Scribed by Takashi Takahashi; Hiroshi Ikeda; Jiro Tsuji


Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
233 KB
Volume
22
Category
Article
ISSN
0040-4039

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✦ Synopsis


SummarE

Zearalenone was synthesized by a general cyclization method of orsellic acid type macrolides having ketone moiety using the intramolecular alkylation of the protected cyanohydrin. This alkylation tolerates the presence of ester group and requires short reaction time.


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