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Volumn 7, Issue 20, 2005, Pages 4407-4410

Asymmetric aza-Henry reactions from N-p-tolylsulfinylimines

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EID: 26444544180     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051580d     Document Type: Article
Times cited : (56)

References (31)
  • 7
    • 0346349375 scopus 로고    scopus 로고
    • (a) A diastereoselective aza-Henry type reaction has been described using α-amidoalkylphenyl sulfones as precursors to generate in situ the corresponding N-acylimines: Foresti, E.; Palmieri, G.; Petrini, M.; Profeta, R. Org. Biomol. Chem. 2003, 1, 4275.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 4275
    • Foresti, E.1    Palmieri, G.2    Petrini, M.3    Profeta, R.4
  • 19
    • 26444532962 scopus 로고    scopus 로고
    • During the preparation of the present manuscript, a case of enantioselective nitro-Manich addition of nitroethane into two alkyl-derived aldimines was published: Anderson, J. C.; Howell, G. P.; Lawrence, R. M.; Wilson C. J. Org. Chem. 2005, 70, 5565. Nevertheless, the authors state the moderate stability of these two prepared aldimines.
    • (2005) J. Org. Chem. , vol.70 , pp. 5565
    • Anderson, J.C.1    Howell, G.P.2    Lawrence, R.M.3    Wilson, C.4
  • 21
  • 26
    • 26444473302 scopus 로고    scopus 로고
    • note
    • tBu) have been explored.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.