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Volumn 57, Issue 3, 2009, Pages 321-323

One-Pot N-Arylation of indoles directly from N-arylsulfonylindoles via consecutive deprotection and SnAr reactions with activated aryl halides

Author keywords

N arylindole; N arylsulfonylindole; One pot reaction

Indexed keywords

HALIDE; INDOLE DERIVATIVE; SULFONIUM DERIVATIVE; SULFONYLINDOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 62549145765     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.57.321     Document Type: Article
Times cited : (7)

References (31)
  • 31
    • 62549150058 scopus 로고    scopus 로고
    • A mixture of N-tosyl-3-methylindole (0.5mmol) and t-BuOK (1.0 mmol) in THF (2.5 ml) was stirred at reflux under argon for 12 h. After cooling, the solvent was evaporated under reduced pressure, and the residue was purified by preparative TLC to give 3-methylindole in a 64% yield.
    • A mixture of N-tosyl-3-methylindole (0.5mmol) and t-BuOK (1.0 mmol) in THF (2.5 ml) was stirred at reflux under argon for 12 h. After cooling, the solvent was evaporated under reduced pressure, and the residue was purified by preparative TLC to give 3-methylindole in a 64% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.