1978
DOI: 10.1002/chin.197828183
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ChemInform Abstract: ACTION OF GRIGNARD REAGENTS AND ARYLLITHIUM ON 1,1‐DISUBSTITUTED CYCLOHEXANE DERIVATIVES

Abstract: Die Cyclohexanderivate (I) und (IIIa) entstehen durch Grignard‐ Reaktionen auf dem angegebenen Weg.

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“…Thiscompound wasprepared according toapublishedmethod [21,22]from morpholine,cyclohexanone and KCN withayield of 81.5 %(m. p. 41 -43°C),IR: 2220 cm -1 ,C =N, str.…”
Section: 221-morpholinocyclohexanecarbonitrilem CC (2)mentioning
confidence: 99%
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“…Thiscompound wasprepared according toapublishedmethod [21,22]from morpholine,cyclohexanone and KCN withayield of 81.5 %(m. p. 41 -43°C),IR: 2220 cm -1 ,C =N, str.…”
Section: 221-morpholinocyclohexanecarbonitrilem CC (2)mentioning
confidence: 99%
“…[11 -13], and incorporation of morpholine groupwithm anypharmacological [15,16]a nd analgesicproperties [17,18]of its derivatives,will havep ronounced effects on the newdrug's activity. Knownp roceduresw ereapplied fort he synthesisof compounds I, II, 1 and 2 withthe appropriatemodifications [21][22][23].…”
Section: 32formalin Testmentioning
confidence: 99%