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Volumn 65, Issue 11, 2009, Pages 2344-2350

General approach to 6-tosyl-2,3,4,5-tetrahydro-1H-1,3-diazepin-2-ones via nucleophile-mediated ring expansion of tetrahydropyrimidines

Author keywords

1,2,3,4 Tetrahydropyrimidin 2 ones; 2,3,4,5 Tetrahydro 1H 1,3 diazepin 2 ones; Ring expansion

Indexed keywords

4 (BENZOYLOXYMETHYL) 6 METHYL 5 TOSYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 [DI(ETHOXYCARBONYL)METHYL] 7 METHYL 6 TOSYL 2,3,4,5 TETRAHYDRO 1H 1,3 DIAZEPIN 2 ONE; 4 CYANO 7 METHYL 5 TOSYL 2,3,4,5 TETRAHYDRO 1H 1,3 DIAZEPIN 2 ONE; 4 HYDROXYMETHYL 6 METHYL 5 TOSYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 4 MESYLOXYMETHYL 6 METHYL 5 TOSYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 6 METHYL 5 TOSYL 4 TOSYLOXYMETHYL 1,2,3,4 TETRAHYDROPYRIMIDIN 2 ONE; 7 METHYL 4 PHENYLTHIO 6 TOSYL 2,3,4,5, TETRAHYDRO 1H 1,3 DIAZEPIN 2 ONE; 9 METHYL 5 METHYLENE 6,8 DITOSYL 1,2,4,5,6,6A,7,10 OCTAHYDRO 1,6 METHANOL[1,3]DIAZEPINO[1,7 E][1,3,5]TRIAZOCINE 3,11 DIONE; NUCLEOPHILE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 59749098713     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.01.015     Document Type: Article
Times cited : (25)

References (25)
  • 2
    • 78549232368 scopus 로고
    • Chem. Abstr. 109 (1988) 54794
    • (1988) Chem. Abstr. , vol.109 , pp. 54794
  • 9
    • 59749098605 scopus 로고    scopus 로고
    • note
    • 1=Me) are readily available.
  • 18
    • 59749101400 scopus 로고    scopus 로고
    • note
    • Formation of ureido-substituted 4,5-dihydrofurans also occurred in the reaction of enolates of other α-substituted carbonyl compounds with tosylurea 3 (our unpublished data).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.