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Naturally occurring oxygen heterocyclics 4-phenyl-5,7-dihydroxy-6-isovaleryl-8-isopentenylcoumarin

โœ Scribed by R.A. Finnegan; Carl Djerassi


Book ID
104249931
Publisher
Elsevier Science
Year
1959
Tongue
French
Weight
192 KB
Volume
1
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


IB a reoent oomnuuicatlonl from this Laboratory it was shorn that the lueeotloidal oonstituent2 mmmnein from the seeds of &mea americana L. possesses struoture I. Through the kind oo-operation of Dr. Murrell P. Morris of the U.S. Department of &riculture Experiment Station In Msyaguee, Puerto Rioo, we have obtained a supply of a yellow toxic prinoiple derived from the pulp of the fruits of the same plant, and the present report Is concerned with ite structure elucidation. Chromatographio purification of the yellow substance aud repeated recrystallisation from various solvents led to homogenous material vith a wide melting point range, apparently due to salvation. The analytical 46


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7-Methyl-4-phenyl-8H-1,3,5,6-dithiadiazo
โœ Dr. G. Ege ๐Ÿ“‚ Article ๐Ÿ“… 1967 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 271 KB ๐Ÿ‘ 1 views

tion of ( ) is explained by the strong reducing action of HGeC13 [?I. The alcohol ( ) is probably formed first and then condenses to give the ether (8). Under the influence of HGeC13 ethers can decompose to alkyl-or arylalkyl-trichlorogermanes and alcoholsW In fact, the reaction o f t h e alcohol (7