𝔖 Bobbio Scriptorium
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Cucurbitacins

✍ Scribed by J. E. Ferguson; R. L. Metcalf


Publisher
Springer
Year
1985
Tongue
English
Weight
452 KB
Volume
11
Category
Article
ISSN
0098-0331

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CUCDRRITACINS Bse the various the Cucurbitaceae. Some have activity.4 Based on dehydrogenation bitter highly toxic principles oocurring in been investigated for their anti-tumor experiments and on the nature of the side chain, a regular tetracyclio triterpenoid carbon skeleton has been assigned to t

The constitutions of the cucurbitacins
✍ W.T. de Koch; P.R. Enslin; K.B. Norton; D.H.R. Barton; B. Sklarz; A.A. Bothner-B πŸ“‚ Article πŸ“… 1962 πŸ› Elsevier Science 🌐 French βš– 324 KB

THE cucurbitacins are M interesting group of bitter the Cucurbitaceae.' A constitution (I) was recently cucurbitacin E. The related cucurbitacin B R = side chain). Cucurbitacins B, D, E and may be represented as in (II, I have all been correlated U.K. 13, Pennsylvania principles found in proposed\*

The stereochemistry of the cucurbitacins
✍ David Lavie; Youval Shvo; Otto Richard Gottlieb πŸ“‚ Article πŸ“… 1960 πŸ› Elsevier Science 🌐 French βš– 341 KB

THE stereochemistry of ring A of some of the cucurbitacins has been discussed in a previous communication. 4 We wish to report now the experiments which led us to present most of the stereochemistry of the four naturally occurring cucurbitacins: elatericin A (Ia), cucurbitacin B (Ib), elatericin B (