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Volumn , Issue 6, 1997, Pages 620-622

A viable route to exo-2-benzyliminobornan-3-ol: A key intermediate in the synthesis of a chiral auxiliary

Author keywords

Benzylamine; Chiral auxiliary; Exo 2 benzyliminobornan 3 ol; Hydroxy N nitroimine; Nitrous oxide

Indexed keywords

BENZYLAMINE DERIVATIVE; BORNANE DERIVATIVE;

EID: 0030859251     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-1404     Document Type: Article
Times cited : (11)

References (24)
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    • note
    • 1 or a number of variants. Subsequently we were likewise unable to make 2 by the literature method.
  • 7
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    • Freeman, J. P. J. Org. Chem. 1961, 26, 4190. Whereas fenchone N-nitroimine appears to be stable indefinitely, the norbornanone analogue has not been isolated.
    • (1961) J. Org. Chem. , vol.26 , pp. 4190
    • Freeman, J.P.1
  • 12
    • 8044220402 scopus 로고
    • Passerini, M. Gazz. Chim. Ital. 1925, 55, 559. Houben, J.; Pfankuch, E. Ber. Dtsch. Chem. Ges. 1927, 60, 586. Houben, J.; Pfankuch, E. Liebigs Ann. Chem. 1930, 483, 271.
    • (1925) Gazz. Chim. Ital. , vol.55 , pp. 559
    • Passerini, M.1
  • 13
    • 84912634385 scopus 로고
    • Passerini, M. Gazz. Chim. Ital. 1925, 55, 559. Houben, J.; Pfankuch, E. Ber. Dtsch. Chem. Ges. 1927, 60, 586. Houben, J.; Pfankuch, E. Liebigs Ann. Chem. 1930, 483, 271.
    • (1927) Ber. Dtsch. Chem. Ges. , vol.60 , pp. 586
    • Houben, J.1    Pfankuch, E.2
  • 14
    • 84911314796 scopus 로고
    • Passerini, M. Gazz. Chim. Ital. 1925, 55, 559. Houben, J.; Pfankuch, E. Ber. Dtsch. Chem. Ges. 1927, 60, 586. Houben, J.; Pfankuch, E. Liebigs Ann. Chem. 1930, 483, 271.
    • (1930) Liebigs Ann. Chem. , vol.483 , pp. 271
    • Houben, J.1    Pfankuch, E.2
  • 18
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    • and also ref 5
    • 2O is lost from N-nitroimines, see: Büchi, G.; Wuest, H. J. Org. Chem. 1979, 44, 4116; and also ref 5.
    • (1979) J. Org. Chem. , vol.44 , pp. 4116
    • Büchi, G.1    Wuest, H.2
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    • Eschenmoser, A. Quart. Rev. 1990, 366. Roth, M.; Dubs, P.; Götschi, E.; Eschenmoser, A. Helv. Chim. Acta 1971, 54, 710.
    • (1990) Quart. Rev. , pp. 366
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    • Thoren, S. Acta Chem. Scand. 1970, 24, 93. Suginome, H.; Satoh, G.; Wang, J. B.; Yamada, S.; Kobayashi, K. J. Chem. Soc., Perkin Trans. 1 1990, 1239. The assignment of configuration to compound 4 (numbering from this paper) and its epimer by Suginome et al. should be reversed.
    • (1970) Acta Chem. Scand. , vol.24 , pp. 93
    • Thoren, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.