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Partial Synthesis of 3′-Hydroxy-2′-deoxy-2″,3″,4″,5″-tetrahydroverrucarin A. Verrucarins and roridins, 38th Communication [1]

✍ Scribed by Eric-Andréa Notegen; Motoo Tori; Christoph Tamm


Publisher
John Wiley and Sons
Year
1981
Tongue
German
Weight
807 KB
Volume
64
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The macrocyclic trichothecene triester 3′‐hydroxy‐2′‐deoxy‐2",3",4",5"‐tetrahydroverrucarin A (37), has been synthesized starting from the sesquiterpene alcohol verrucarol (3), adipic acid and a derivative of mevalonic acid (14). The latter has been prepared from 4‐(tetrahydro‐2‐pyranyloxy)‐2‐butanone (9).


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ChemInform Abstract: Simple Three-Compon
✍ T. A. SILINA; N. A. PULINA; L. F. GEYN; V. L. GEYN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Simple Three-Component Synthesis of 4-Acyl-5-phenyl-1-(2-hetaryl)-3-hydroxy-3-pyrrolin-2-ones. -Thermal three-component cyclocondensation of methyl acylpyruvate (I), benzaldehyde (II) and hetarylamines (III) furnishes the novel 4-acyl-5-phenylpyrrolinones-2 (IV) containing a hetaryl group at the N(