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Volumn 127, Issue 13, 2005, Pages 4592-4593

Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL ALCOHOL; BORANE DERIVATIVE; INDOLE DERIVATIVE; PALLADIUM; TRIETHYLBORANE; UNCLASSIFIED DRUG;

EID: 16844383145     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0501161     Document Type: Article
Times cited : (342)

References (36)
  • 2
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press: London
    • (b) Sundberg, R. J. Indoles; Academic Press: London, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 26
    • 16844370642 scopus 로고    scopus 로고
    • note
    • 3B as a Lewis acid catalyst is improbable.
  • 27
    • 16844380110 scopus 로고    scopus 로고
    • note
    • Use of allyl chloride, in place of allyl alcohol, under the conditions resulted in no reaction.
  • 28
    • 16844383591 scopus 로고    scopus 로고
    • note
    • The structure of 2m was deduced on the basis of NOE experiments. Some typical data are given in Scheme 1.
  • 29
    • 0028068032 scopus 로고
    • Phosphoric acid promoted hydroamination across the C2-C3 bond provides exo- and endo-pyrroloindole in a 9:1 ratio: Bruncko, M.; Crich, D.; Samy, R. J. Org. Chem. 1994, 59, 5543.
    • (1994) J. Org. Chem. , vol.59 , pp. 5543
    • Bruncko, M.1    Crich, D.2    Samy, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.