Saturated nitrogen ring compounds

Пономарев, А. А.; Кривенько, А. П.; Noritsina, M. V.

doi:10.1007/bf00468342

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IV Ix:r=hn=i;1

Experimental Chemical Part1

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1969

2015

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Cited by 3 publications

(4 citation statements)

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“…The reactions were performed at a temperature of 100~ and a hydrogen pressure of 10 MPa in an alcohol solution of ammonia or methylamine in the presence of Raney nickel catalyst [4,5].…”

Section: IV Ix:r=hn=i;mentioning

confidence: 99%

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Synthesis and anticholinesterase activity of amines and diamines of the furan series and their salts

1997

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“…The reactions were performed at a temperature of 100~ and a hydrogen pressure of 10 MPa in an alcohol solution of ammonia or methylamine in the presence of Raney nickel catalyst [4,5].…”

Section: IV Ix:r=hn=i;mentioning

confidence: 99%

“…The synthesis of 2-(2-furfuryl)eycloalkylamines I-IV was performed according to [4,5]. Aminonitriles XII, XIII and diamines XIV, XV were obtained as described elsewhere [6].…”

Section: Experimental Chemical Partmentioning

confidence: 99%

Synthesis and anticholinesterase activity of amines and diamines of the furan series and their salts

1997

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“…Cleavage of 2-aminoalkylfurans has been carried out employing catalytic hydrogenation conditions yielding alkylpyrroles (6), alkylpyrrolidines (6, 7), and a-pyrrolidyl-3-alkanols (8). Cyclic ethers such as tetrahydrofuran have been cleaved by acid halides to yield esters of 4-halo-I-pentanol and 5-halo-2-pentanol(9).…”

mentioning

confidence: 99%

“…: C, 51.17; H, 9.74; N,8.60.5-(3-Chloropropyl)-3-methyl-2~xazolid~one (IIa)-Asolution of N-methyltetrahydrofurfurylamine (57.6 g., 0.5 mole) and triethylamine (50.5 g., 0.5 mole) in toluene (200 ml.) was added to a stirred solution of phosgene (99 g., 1.0 mole) in toluene (400 ml.)…”

mentioning

confidence: 99%