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Volumn 42, Issue 9, 2001, Pages 1661-1663

Hydroxylation of olefins using molecular oxygen via alkylboronic esters

Author keywords

Alcohols; Amines; Boron and compounds; Hydroxylation; Olefins

Indexed keywords

ALCOHOL DERIVATIVE; ALKENE DERIVATIVE; ALKYL GROUP; BORONIC ACID DERIVATIVE; OXYGEN;

EID: 0035951972     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)02337-6     Document Type: Article
Times cited : (6)

References (27)
  • 1
    • 0038643951 scopus 로고    scopus 로고
    • In Eds. Handbook of reagents for organic synthesis. Wiley: Chichester
    • In Oxidizing and Reducing Agents; Burke, S. D.; Danheiser, R. L.; Eds. Handbook of reagents for organic synthesis. Wiley: Chichester, 1999.
    • (1999) Oxidizing and Reducing Agents
    • Burke, S.D.1    Danheiser, R.L.2
  • 9
    • 0343969805 scopus 로고    scopus 로고
    • US Patent, 3,439,046, 1969
    • Brown, H. C. US Patent, 3,439,046, 1969.
    • Brown, H.C.1
  • 13
  • 21
    • 0343098019 scopus 로고    scopus 로고
    • 1H NMR analyses in selected cases of the crude mixtures showed the presence of minor amounts of isomers alongside with the desired product.
    • 1H NMR analyses in selected cases of the crude mixtures showed the presence of minor amounts of isomers alongside with the desired product.
  • 23
    • 0342663710 scopus 로고    scopus 로고
    • 13C NMR, MS) were obtained for all compounds.
    • 13C NMR, MS) were obtained for all compounds.
  • 24
    • 0342663729 scopus 로고    scopus 로고
    • For this experiment a 4-fold excess of borane reagent was used. The decomplexation of the aminoborane intermediate was realized in EtOH at reflux under 24 hours.
    • For this experiment a 4-fold excess of borane reagent was used. The decomplexation of the aminoborane intermediate was realized in EtOH at reflux under 24 hours.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.