Showing papers by "Roussel Uclaf published in 1966"
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14 citations
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19 Jan 19667 citations
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10 Aug 19666 citations
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21 Jun 1966TL;DR: In this paper, a novel compound of the general formula (in which R1 and R2 represent alkyl groups contain 1-5 carbon atoms) is obtained by condensing 9 - isopropylidene - 9,10 - dihydroanthracene - 10-carboxylic acid chloride with a b -aminoethanol of the formula wherein R 1 and R 2 are as defined above.
Abstract: Novel compounds of the general formula (in which R1 and R2, which may be the same or different, represent alkyl groups contain 1-5 carbon atoms) are obtained by condensing 9 - isopropylidene - 9,10 - dihydroanthracene - 10-carboxylic acid chloride with a b -aminoethanol of the formula wherein R1 and R2 are as defined above, e.g. b -dimethylamino-, b -diethylamino-, b -methylethylamino-, b -methylbutylamino-, b -methylisopropylamino or b -ethylbutylaminoethanol. The products form non-toxic acid addition salts. 9 - Isopropylidene - 9,10 - dihydroanthracene - 10 - carboxylic acid chloride is obtained from the corresponding acid with a dehydrating agent, e.g. thionyl chloride, phosphorus trichloride or phosphorus pentachloride. Pharmaceutical compositions containing the above novel compounds and having a spasmolytic activity are administered orally, parenterally, or rectally.
4 citations
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28 Jun 19662 citations
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01 Feb 19662 citations
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06 Sep 19661 citations
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21 Dec 1966•
17 Oct 1966••
TL;DR: In this article, the presence of a mixture of cholesterol, desmosterol, 7-dehydrocholesterol and 7 dehydrodes mosterol was observed in the blood and organs of rats treated by Δ 7 and Δ 24 -reductase inhibitors.
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07 Dec 1966TL;DR: In this paper, the C-CEPHALOSPORINE FAMILY and their pre-parparation is discussed in detail, and a novel procedure for the preparation of the SAID COMPOUNDS is described.
Abstract: LACTONES OF 2-(CARBONYL-AMINO-METHYL)-5-HYDROXYMETHYL-3,6-DIHYDRO-2H-1,3-THIAZINE-4 -CARBOXYLIC ACIDS USEFUL AS INTERMEDIATES FOR ANTIBIOTICS OF THE C-CEPHALOSPORINE FAMILY AND THEIR PREPARATION. THE INVENTION RELATES TO NOVEL DIHYDRO-1,3-THIAZINE COMPOUNDS OF THE FORMULA 2-(R-OOC-CH(-Y)-),7-(O=)-1,2,5,7-TETRAHYDRO-4H-FURO(3,4-D) (3,1)THIAZINE WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF ALKYL AND ARALKYL, Y IS SELECTED FROM THE GROUP CONSISTING OF -HN-AC, PHTHALIMIDO AND-NH-R'',R'' IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL AND ARALKYL AND AC IS THE ACYL RADICAL OF AN ORGANIC CARBOXYLIC ACID OF 1 TO 18 CARBON ATOMS AND TO A NOVEL PROCESS FOR THE PREPARATION OF THE SAID COMPOUNDS.
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07 Mar 1966