66-28-4Relevant articles and documents
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Kreis et al.
, p. 593,598 Anm.22 (1957)
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THERMAL TRANSFORMATION OF CARDIAC GLYCOSIDES II. ACIDLESS HYDROLYSIS OF LABILE GLYCOSIDES IN AQUEOUS ALCOHOLIC SOLUTIONS AND PROSPECTS FOR ITS UTILIZATION
Makarevich, I. F.,Tishchenko, A. A.,Terno, I. S.
, p. 53 - 55 (2007/10/02)
The thermal transformations of cardiac glycosides in neutral alcoholic solutions have been investigated.The kinetics of their acidless hydrolysis at 100 and 142 deg C and the activation energy of the process have been studied.The possibility has been shown of the stepwise hydrolysis of natural trisdigitoxosides with the production of difficulty available mono- and bisdigitoxosides.The following were used as the objects of investigation: convallatoxin, glucostrophanthidin, cheirotoxin, desglucocheirotoxin, erycordin, erysimin, erysimoside, digitoxin, and cymarin.
NEOCONVALLOSIDE - A CARDENOLIDE GLYCOSIDE FROM PLANTS OF THE GENUS Convallaria
Komissarenko, N. F.,Stupakova, E. P.
, p. 186 - 189 (2007/10/02)
In a study of the epigeal part and seeds of Convallaria keiskei, C. majalis, and C. transcaucasica, in addition to lokundjoside, convalloside, convallotoxoloside, and neovallotoxoloside, we have isolated the previously unknown glycoside neoconvalloside, for which, on the basis of the physicochemical properties of the compound and of the products of its chemical transformations, the structure of strophanthidin 3-O- 2)-α-L-rhamnopyranoside> has been esteblished.
Active principles of Cheiranthus cheiri L..
SCHINDLER
, p. 512 - 514 (2007/10/07)
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