메뉴 건너뛰기




Volumn 43, Issue 37, 2002, Pages 6579-6582

Convenient indole synthesis from ethynylanilines with a polymer-supported fluoride

Author keywords

Cyclization reaction; Ethynylanilines; Indole synthesis; Polymer supported fluoride

Indexed keywords

ALKYL GROUP; ANILINE DERIVATIVE; ARGON; CARBONYL DERIVATIVE; CHLORINE DERIVATIVE; FLUORIDE; FLUORIDE ION; FUNCTIONAL GROUP; INDOLE DERIVATIVE; NITRILE; PHENYL GROUP; POLYMER; RESIN;

EID: 0037048480     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01439-9     Document Type: Article
Times cited : (26)

References (16)
  • 14
    • 0011224646 scopus 로고    scopus 로고
    • General procedure for the cyclization reaction of ethynylanilines with polymer-supported fluoride. A mixture of ethynylanilines (1 mmol), polymer-supported fluoride (1.2 mmol, 300 mg), and dry MeCN was heated under an argon atmosphere at 100°C for 24 h in a sealed apparatus. After cooling, the mixture was filtered and the resin was washed with AcOEt. The residue obtained from the filtrate was purified by column chromatography.
    • General procedure for the cyclization reaction of ethynylanilines with polymer-supported fluoride. A mixture of ethynylanilines (1 mmol), polymer-supported fluoride (1.2 mmol, 300 mg), and dry MeCN was heated under an argon atmosphere at 100°C for 24 h in a sealed apparatus. After cooling, the mixture was filtered and the resin was washed with AcOEt. The residue obtained from the filtrate was purified by column chromatography.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.