New approach to 5-arylsulfonyl-substituted 1,2-dihydropyrimidin-2-ones via base-induced chloroform elimination from 4-trichloromethyl-1,2,3,4- tetrahydropyrimidin-2-ones

Tetrahedron

Volumn 66, Issue 35, 2010, Pages 7219-7226

  Fesenko, Anastasia A ^a   Shutalev, Anatoly D ^a  

^a MIREA RUSSIAN TECHNOLOGICAL UNIVERSITY   (Russian Federation)

Author keywords

5 Arylsulfonyl 1,2,3,4 tetrahydropyrimidin 2 ones; 5 Arylsulfonyl 1,2 dihydropyrimidin 2 ones; Aromatization; Ureidoalkylation

Indexed keywords

1,2 DIHYDROPYRIMIDIN 2 ONE DERIVATIVE; 4 (TRICHLOROMETHYL) 6 METHYL 5 PHENYLSULPHONYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 (TRICHLOROMETHYL) 6 METHYL 5 TOSYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 (TRICHLOROMETHYL) 6 PHENYL 5 PHENYLSULPHONYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 (TRICHLOROMETHYL) 6 PHENYL 5 TOSYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 METHYL 5 PHENYLSULPHONYL 1,2 DIHYDROPYRIMIDIN 2 ONE; 4 METHYL 5 TOSYL 1,2 DIHYDROPYRIMIDIN 2 ONE; 4 PHENYL 5 PHENYLSULPHONYL1,2 DIHYDROPYRIMIDIN 2 ONE; 4 PHENYL 5 TOSYL 1,2 DIHYDROPYRIMIDIN 2 ONE; 4 TRICHLOROMETHYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE DERIVATIVE; CHLOROFORM; KETONE DERIVATIVE; N [(1 ACETOXY 2,2,2 TRICHLORO)ETHYL]UREA DERIVATIVE; PYRIMIDINONE DERIVATIVE; UNCLASSIFIED DRUG; UREA DERIVATIVE;

ARTICLE; CYCLIZATION; ELIMINATION REACTION; PRIORITY JOURNAL; SYNTHESIS;

EID: 77955422746     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.06.058     Document Type: Article

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