메뉴 건너뛰기




Volumn 47, Issue 25, 2006, Pages 4245-4248

Regioselective synthesis of N-substituted-4-substituted isothiazolidine-1,1-dioxides

Author keywords

Cyclizations; Epoxides; Ring opening reactions; Sulfonamides

Indexed keywords

EPOXIDE; ISOTHIAZOLE DERIVATIVE; OXIDE; SULFONAMIDE;

EID: 33646527790     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.04.038     Document Type: Article
Times cited : (9)

References (14)
  • 12
    • 33646521112 scopus 로고    scopus 로고
    • note
    • For initial studies, N-benzyl methanesulfonamide (4, R = Bn) was prepared in almost quantitative yield by reaction of benzylamine and methanesulfonyl chloride in THF, in the presence of triethylamine.
  • 13
    • 33646497502 scopus 로고    scopus 로고
    • note
    • Determined by chiral HPLC. Conditions, Column-Chiral AD; eluant 20% iso-propyl alcohol in hexanes containing 0.1% TFA; Retention times-major = 30.5 min, minor = 34.0 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.