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Structure and Synthesis of Novel C12 Terpenoids from Quince Fruit (Cydonia oblonga MILL.)

✍ Scribed by Sina Escher; Yvan Niclass


Publisher
John Wiley and Sons
Year
1991
Tongue
German
Weight
680 KB
Volume
74
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The structure and synthesis of novel irregular C~12~ terpenoids isolated from quince fruit (Cydonia oblonga MILL.) are described: quince oxepine (= (E)‐2,3,6,7‐tetrahydro‐4‐methyl‐2‐(3‐methylbuta‐1,3 dienyl)oxepine; 3) and the quince oxepanes as a 1:1 mixture of cis‐ and trans‐isomers (= cis‐ and trans‐(E)‐4‐methyl‐2‐(3‐methylbuta‐1,3‐dienyl)oxepane; 4 and 5, resp.). The absolute configurations of the natural compounds have not been determined due to the minute amounts available, but both relative and absolute configurations of synthetic 4 and 5 were established by chemial correlation with (R)‐pulegone.


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Structure and synthesis of two novel ion
✍ Regula Näf; Alain Velluz; René Decorzant; Ferdinand Näf 📂 Article 📅 1991 🏛 Elsevier Science 🌐 French ⚖ 246 KB

S~lmmary Two new lonone-type compounds (1 and 2) were Isolated from quince brandy (Cydon~ oblongn Ml1 ) and their structures deduced from spectroscopic data and confumed by synthe~l~ 13C-, 'H-NMR dnd MS data as well as olfactlve propemes of 1 and 2 are given In the dnalysls of the brdndy of quince f