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Acta Chimica Sinica ›› 1959, Vol. 25 ›› Issue (3): 146-151. Previous Articles Next Articles
于同隐1, 崔惠卿2, 黄鸣玉3
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YU TUNG-YIN1, TSWEI HUI-CHING2, HUANG MIN-YUH3
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A aeries of α-mothyl-β-alkylpiperidinos were synthosizo:l in low yields by reductive cyclization of tho conosponding γ-cyanokotonoa with sodium and butyl alcohol.These cyanokotones were in turn preparod by cyanoothylation of α-allcyl-acetoacetic esters with subsequent kotonic liydrolysie.Tho chief by-products isolated were 6-amino-3-alkyl hexanol-2.
YU TUNG-YIN, TSWEI HUI-CHING, HUANG MIN-YUH. SYNTHESES OF α-METHYL-β-ALKYLPIPERIDINES[J]. Acta Chimica Sinica, 1959, 25(3): 146-151.
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