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Volumn 52, Issue 49, 2011, Pages 6646-6648

Catalytic monosilylation of 1,2-diols

Author keywords

1,2 Diols; Chemoselectivity; Dimethyltin dichloride; Silylation

Indexed keywords

1,2 DIOL DERIVATIVE; ALCOHOL DERIVATIVE; METAL COMPLEX; UNCLASSIFIED DRUG;

EID: 80555148166     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.10.016     Document Type: Article
Times cited : (14)

References (34)
  • 13
    • 23644434948 scopus 로고    scopus 로고
    • To avoid overacylation, excess amounts of diols have been often used
    • To avoid overacylation, excess amounts of diols have been often used: S. Takahashi, T. Katagiri, and K. Uneyama Chem. Commun. 2005 3658 3660
    • (2005) Chem. Commun. , pp. 3658-3660
    • Takahashi, S.1    Katagiri, T.2    Uneyama, K.3
  • 16
    • 3042673565 scopus 로고    scopus 로고
    • Review
    • Review: R.D. Crouch Tetrahedron 60 2004 5833 5871
    • (2004) Tetrahedron , vol.60 , pp. 5833-5871
    • Crouch, R.D.1
  • 33
    • 0004223731 scopus 로고
    • Organotins are known to be toxic at relatively low levels of exposure, not only to marine invertebrates but also for mammals and other animals. The most toxic organotin compounds are the trialkyltin compounds, with the ethyl derivative in each group being reported as the most toxic. See: Logos Press London
    • Organotins are known to be toxic at relatively low levels of exposure, not only to marine invertebrates but also for mammals and other animals. The most toxic organotin compounds are the trialkyltin compounds, with the ethyl derivative in each group being reported as the most toxic. See: R.C. Poller The Chemistry of Organotin Compounds 1970 Logos Press London
    • (1970) The Chemistry of Organotin Compounds
    • Poller, R.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.