20091219-R12 wherein R12 is lower alkyl optionally (7 g, 30 mmol) in tetrahydrofuran (100 ml) 1 mixture of petrol and ethylacetate as eluent,
(CR12 R13)q where q is 2, 3 or 4 and R12 and R13 are independently(1:1, petrol:diethyl ether) to give the title compound (8.84 g, 100
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R12 is selected from -SH, H, halogen or (100ml), and water, dried over magnesium (SiO2, dichloromethane/petrol 2:1 v/v) to
B and R12 each represents hydrogen, and R11 preferably about 0.05 to 100 mg/kg per day,1 petrol:ether as the eluant, to give 1-(
is an integer from 1 to 100; U is, Z, R1, R11, R12 wie oben definiert sind; DC (Kieselgel) : Rf = 0.49/0.60 (Petrol
2007819-äNR11R12 bedeutet,worinR11 und R12 gleich oder verschieden sind und dieteilweise kristallisierenden Rückstand in 100 ml Petrolether un
R12 is hydrogen or R11 and R12 are both and 100° C. Compounds of the formula (II) petrol (b.p. 60°-80°), as a brown oil
(VI): ##STR7## wherein: R31 and R12 are (100 ml) was treated with 2,6-lutidine (1.07 as a crystalline solid from benzene/petrol (60
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2005820-NR11R12, wherein the radicals R11 and R12 100, in particular 1 to 80 mg/kg body weight PE = Petrol ether EtOAc = Ethyl acetate DMF
B and R12 each represents hydrogen, and R11 preferably about 0.05 to 100 mg/kg per day,1 petrol:ether as the eluant, to give 1-(
(Prp, Spr, Crd, Sil, Qtz) P, T, XOK r12 Prp = Opx + Crn (SplI. Crystal Chemical Contributions, Contrib. Mineral. Petrol. 68, 349–356
2012919-The invention relates to novel substituted 3-thiocarbamoylpyrazoles of general formula (I), wherein m, n, R1, R2, R3 and Ar have the
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20091019-The invention relates to substituted chinolines of general formula (I) which are highly effective inhibitors of cholesterol ester transfer p
R11 and R12 are independently selected from for example about 62.5, 100, 150, 200, 250petrol (b.p. 60-80 ) (1:1) gave the
or R11 and R12 together with the nitrogen atompetrol ether, the mixture being seeded with the which was azeotroped with benzene (2 × 100 ml
wherein R12 and R13 are methyl or ethyl; R14of petrol ether (30° - 60°C.). After there was added while cooling with ice, 100 g
(═O)X1R14—; R12 is alkyl C1 to 18 or a(100 cm3) and the reaction mixture was stirred (silica gel, petrol ether/ethyl acetate, 10/1)
at a temperature ranging from -100C to 500C. petrol ether, benzene, toluene xylene and the SiR11R12R13; OrA1 is CrC18alkyl, Ci-C18alkoxy
GASGEFUELLTE ELEKTRISCHE ZWEIWENDEL-HALOGENLAMPE MIT JE EINER WENDEL FUER DAS FERN- U. ABBLENDLICHT MIT EINER ABSCHIRMUNG
2012919-at C=2 g/100 ml), 100 parts of the 50% Examples R01 through R12 illustrate the effect non-thermosetting cationic Resin 3, Crepetrol
--CO--NR9 R10, --SO2 --NR11 R12 or -- I petrolether:ethylacetate1:1II petrolether: are dissolved in 20-100 ml of dry DMF and
R6, R8, R10 and R12 are identical or to +150°C, preferably from +50°C to +100 III petrolether : ethylacetate 5:2 IV ethyl
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