The raspailynes (novel long-chain enol cthcrs of glycerol having the enol ether double bond conjugated, in sequence, to an acetylenic and an olefinic bond, isolated from the North-East-Atlantic sponges Raspilia prtmila and R.rumo.sa) are stable under normal hydrolytic conditions for enol ethers. In
โฆ LIBER โฆ
Raspailynes, Novel Long-Chain Acetylenic Enol Ethers of Glycerol from the Marine Sponges Raspailia pumila and Raspailia ramosa
โ Scribed by Graziano Guella; Ines Mancini; Francesco Pietra
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- German
- Weight
- 753 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0018-019X
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โฆ Synopsis
We loosely use here the term 'higher polarity' to mean a higher retention time on silica-gel chromatography. For convenience, id1 raspailynes and derivatives thereof are numbered as shown in the Formulae 1-14 Systematic names are given in the Summary and Exper. Part.
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Likely, the absolute configuration of the raspailynes could have otherwise been determined by Snatzke's circular dichroic method in the presence of the Mo2(O2CCH,), complex . We thank Prof. G. Snatzke for suggesting us this possibility.
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Oxidative Breaking of Long-Chain Acetyle
โ
Graziano Guella; Ines Mancini; Francesco Pietra
๐
Article
๐
1987
๐
John Wiley and Sons
๐
German
โ 745 KB