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Volumn 64, Issue 13, 1999, Pages 4959-4961

A convenient trimethylsilylthioxy-dehalogenation reaction for the preparation of functionalized thiols

Author keywords

[No Author keywords available]

Indexed keywords

THIOL DERIVATIVE; TRIMETHYLSILYL DERIVATIVE;

EID: 0033603618     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo990076h     Document Type: Article
Times cited : (69)

References (23)
  • 4
  • 14
    • 0345228738 scopus 로고    scopus 로고
    • The thiol ester method: see ref 1
    • (b) The thiol ester method: see ref 1.
  • 17
    • 0345660667 scopus 로고    scopus 로고
    • Hu, J.; Fox, M. A. Unpublished results
    • Hu, J.; Fox, M. A. Unpublished results.
  • 20
    • 0345660665 scopus 로고    scopus 로고
    • note
    • Disulfides are observed as impurities in the crude thiol products (3-10% for reactions of about 0.5 mmol scales). They are most likely formed by autooxidation during the workup and isolation process.
  • 22
    • 0342459190 scopus 로고
    • Laibinis, P. E.; Whitesides, G. M.; Allara, D. L.; Tao, Y.-T.; Parikh, A. N.; Nuzzo, R. G. J. Am. Chem. Soc. 1991, 113, 7152. Contact angles measured by a sessile drop technique for a bare polycrystalline gold surface, for a preformed 1-decanethiol SAM, and for an in situ prepared SAM from 1-bromodecane are 58 ± 1.9°, 96.4 ± 3.7°, and 94.1 ± 1.8°, respectively.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 7152
    • Laibinis, P.E.1    Whitesides, G.M.2    Allara, D.L.3    Tao, Y.-T.4    Parikh, A.N.5    Nuzzo, R.G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.