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Volumn 2, Issue 25, 2000, Pages 4107-4109

Highly selective aziridination of imines using trimethylsilyldiazomethane and applications of C-silylaziridines in synthesis

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Indexed keywords


EID: 0000415479     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol006772h     Document Type: Article
Times cited : (73)

References (45)
  • 38
    • 0002623376 scopus 로고
    • Dondoni, A., Ed; JAI Press: London
    • TMSD is a safe and stable commercially available diazo compound. For a review on TMSD, see: Shioiri, T.; Aoyama, T. In Advances in Using Synthons in Organic Chemistry; Dondoni, A., Ed; JAI Press: London, 1993; Vol. 1, pp 51-101.
    • (1993) Advances in Using Synthons in Organic Chemistry , vol.1 , pp. 51-101
    • Shioiri, T.1    Aoyama, T.2
  • 39
    • 0042612187 scopus 로고    scopus 로고
    • note
    • For examples of decomposition of triazoline to the corresponding C-silylaziridine with silica gel, see refs 8e and 8f.
  • 40
    • 0042612189 scopus 로고    scopus 로고
    • note
    • See ref 7. For the rare examples where trans aziridines are the main isomers, see refs 7o and 7p.
  • 41
    • 0001443339 scopus 로고    scopus 로고
    • Recently TBAT has been introduced and, being non-hygroscopic, non-basic, and soluble in a wide range of organic solvents, has proved to be very effective for Si-C bond cleavage. See: Pilcher, A. S.; DeShong, P. J. Org. Chem. 1996, 61, 6901.
    • (1996) J. Org. Chem. , vol.61 , pp. 6901
    • Pilcher, A.S.1    DeShong, P.2
  • 42
    • 0041610303 scopus 로고    scopus 로고
    • note
    • Full details will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.