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Volumn 21, Issue 10, 1998, Pages 617-621

Regio- and stereoselective alcoholysis of (R)-styrene oxide with bis-tributyltin oxide and bis-chlorodibutyltin oxide

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[No Author keywords available]

Indexed keywords


EID: 0032346355     PISSN: 07921241     EISSN: 21910219     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (25)
  • 18
    • 0000710110 scopus 로고
    • Qualitative estimation of the acidity of organotin compounds was made using the phosphine oxide IR frequency method, as reported by Vedejs, E.; Erdman, D. E.; Powell, D. R. J. Org. Chem., 58, (1993), 2840.
    • (1993) J. Org. Chem. , vol.58 , pp. 2840
    • Vedejs, E.1    Erdman, D.E.2    Powell, D.R.3
  • 20
    • 19444378284 scopus 로고    scopus 로고
    • note
    • In the absence of BBTO, the regioisomers 4 and 5 were obtained in only 20% isolated yield, recovering 80% of the starting styrene oxide.
  • 24
    • 19444376032 scopus 로고    scopus 로고
    • note
    • In the ring-opening reactions of (R) styrene oxide catalyzed by 3, the study of the enantiomeric excess was done only with stereoisomers 4a and 4b, since 2-isopropoxy-2-phenylethanol (6) was isolated in low yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.