1966
DOI: 10.1021/jo01343a512
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Reaction of 1-(p-Chlorophenyloxycarbonyl)-azetidine with Aromatic Amines

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Cited by 10 publications
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“…Attempted purification by flash silica column chromatography failed. Separation by reversed phase preparative HPLC on silica gel (eluting with 80 : 20 MeOH-H 2 O at a flow rate of 15 ml min Ϫ1 ) gave unreacted starting material (HPLC yield: 51%), then 1-( (20), 279 (100), M ϩ 1, 30 Si, 29 Si and 28 Si, respectively]. Finally 1-(3trimethylsilyl-4-methoxyphenyl)-3,4,5,6-tetrahydropyrimidin-2(1H )-one 12h (HPLC yield: 26%) was eluted contaminated with the 2-isomer 12g.…”
Section: -(4-methoxy-2-trimethylsilylphenyl)-3456-tetrahydropyrimidin...mentioning
confidence: 99%
“…Attempted purification by flash silica column chromatography failed. Separation by reversed phase preparative HPLC on silica gel (eluting with 80 : 20 MeOH-H 2 O at a flow rate of 15 ml min Ϫ1 ) gave unreacted starting material (HPLC yield: 51%), then 1-( (20), 279 (100), M ϩ 1, 30 Si, 29 Si and 28 Si, respectively]. Finally 1-(3trimethylsilyl-4-methoxyphenyl)-3,4,5,6-tetrahydropyrimidin-2(1H )-one 12h (HPLC yield: 26%) was eluted contaminated with the 2-isomer 12g.…”
Section: -(4-methoxy-2-trimethylsilylphenyl)-3456-tetrahydropyrimidin...mentioning
confidence: 99%