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Volumn 62, Issue 14, 2006, Pages 3242-3247

A simple iodination protocol via in situ generated ICl using NaI/FeCl 3

Author keywords

Iodination; Iodo cycloalkanones; Iodoindoles; Silyl enol ether

Indexed keywords

2 BROMO 2 (2 ALLYL) 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEXANONE; 2 BROMO 2 (2 ALLYL) 3 METHYL 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEXANONE; 2 IODO 2 (2 ALLYL) 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEPTANONE; 2 IODO 2 (2 ALLYL) 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOPENTANONE; 2 IODO 2 (2 ALLYL) 3 METHYL 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEXANONE; 2 IODO 2 (2,3 BUTANIENYL) 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEXANONE; 2 IODO 3 METHYL 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEXANONE; 3 IODO 3 METHYL 3 (4 TRIMETHYLSILYL 3 BUTYNYL) 1 CYCLOHEPTANONE; AROMATIC COMPOUND; FERRIC CHLORIDE; SILANE DERIVATIVE; SODIUM; UNCLASSIFIED DRUG;

EID: 33644891402     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.01.067     Document Type: Article
Times cited : (30)

References (30)
  • 19
    • 33644927158 scopus 로고    scopus 로고
    • note
    • The silyl-enol ether 1a was prepared in 92% yield (2.6 g) via CuI promoted 1,4-addition of 3-methyl-2-cyclohexene-1-one (1.0 g, 9.1 mmol) with freshly prepared Grignard using 4-bromo-1-trimethylsilyl-1-butyne (5.8 g, 27.2 mmol) and Mg turnings (1.32 g, 54.5 mmol) in dry THF.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.