1972
DOI: 10.1002/chin.197220217
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ChemInform Abstract: NUCLEOPHILER AUSTAUSCH DER HYDROXYL‐GRUPPE DURCH BROM IN 1‐AMINOMETHYLCYCLOHEXANOL

Abstract: Durch Reduktion von Cyclohexanon‐cyanhydrin (I) mit Lithium‐aluminiumhydrid in Äther erhält man das 1‐Aminomethyl‐cyclohexanol (II) (Ausbeute 79%), das mit 48%iger Bromwasserstoffsäure in das Hydrobromid (III) übergeführt wird.

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“…Colourless oil. 13 (7) 50 values were determined at 378 in 0.08m KH 2 PO 4 /K 2 HPO 4 or NaH 2 PO 4 /Na 2 HPO 4 buffer, with 4-nitrophenyl b-d-glucopyranoside as the substrate ([S] % K M ). 15 3038w, 2954w, 1751s, 1594w, 1443w, 1377m, 1248s, 1131w, 1064m, 1033m, 978w, 932w, 896w, 846w.…”
Section: Experimental Partmentioning
confidence: 99%
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“…Colourless oil. 13 (7) 50 values were determined at 378 in 0.08m KH 2 PO 4 /K 2 HPO 4 or NaH 2 PO 4 /Na 2 HPO 4 buffer, with 4-nitrophenyl b-d-glucopyranoside as the substrate ([S] % K M ). 15 3038w, 2954w, 1751s, 1594w, 1443w, 1377m, 1248s, 1131w, 1064m, 1033m, 978w, 932w, 896w, 846w.…”
Section: Experimental Partmentioning
confidence: 99%
“…R f (hexane/AcOEt 3 : 1) 0. See a. IC 50 Values were determined at 378 in 0.08m citric acid/Na 2 HPO 4 buffer (pH 4.2). 1 H-NMR (300 MHz, CDCl 3 ): 5.33 (t, J 9.7, HÀC(5)); 5.15 (d, J 9.7, HÀC(4)); 5.13 (dd, J 10.6, 9.3, HÀC(6)); 4.07 (dd, J 11.5, 5.6, CHÀC(7)); 3.90 (dd, J 11.5, 3.1, CH'ÀC(7)); 2.40 ± 2.29 (m, HÀC (7) (7)); 3.64, (dd, J 11.5, 5.9, CH'ÀC (7)); 3.62 (d, J 9.3, HÀC(4)); 3.43 (t, J 9.0, irrad.…”
Section: Experimental Partmentioning
confidence: 99%
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