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The use of d-ribonolactone in organic synthesis. I. total synthesis of (−)-litsenolides C1 and C2.

✍ Scribed by Shin-Yih Chen; Madeleine M. Joullie

Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
225 KB
Volume
24
Category
Article
ISSN
0040-4039

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✦ Synopsis

D-Ribonolactone, an inexpensive, commercially available sugar, has been transformed stereoselectively into naturally occurring lactones, the litsenolides Cl and C2.

During the course of chemical studies on Litsea Japonica (Thunb) Juss., a plant

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