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Volumn 9, Issue 10, 2007, Pages 2023-2026

Dinuclear zinc-catalyzed enantioselective aza-henry reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALKANE; HETEROCYCLIC COMPOUND; IMINE; ZINC DERIVATIVE;

EID: 34249275662     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070618e     Document Type: Article
Times cited : (97)

References (31)
  • 20
    • 34249330714 scopus 로고    scopus 로고
    • For a discussion of dual activation with polynuclear catalysts, see:, 21. And concerning the aza-Henry reaction, see
    • For a discussion of dual activation with polynuclear catalysts, see: Shibasaki, M.; Kanai, M.; Matsunaga, S. Aldrichimica Acta 2006, 39, 21. And concerning the aza-Henry reaction, see: ref 2a.
    • (2006) Aldrichimica Acta , vol.39
    • Shibasaki, M.1    Kanai, M.2    Matsunaga, S.3
  • 23
    • 34249289061 scopus 로고    scopus 로고
    • For an example of two-point binding with catalyst la, see: ref 3b
    • For an example of two-point binding with catalyst la, see: ref 3b.
  • 24
    • 0034647015 scopus 로고    scopus 로고
    • For a review on nitrogen protection, see
    • For a review on nitrogen protection, see: Theodoridis, G. Tetrahedron 2000, 56, 2339.
    • (2000) Tetrahedron , vol.56 , pp. 2339
    • Theodoridis, G.1
  • 26
    • 33744733390 scopus 로고    scopus 로고
    • For other applications of α,β-unsaturated carbamate-protected imines, see: a
    • For other applications of α,β-unsaturated carbamate-protected imines, see: (a) Ting, A.; Lou, S.; Schaus, S. E. Org. Lett. 2006, 8, 2003.
    • (2003) Org. Lett , vol.2006 , pp. 8
    • Ting, A.1    Lou, S.2    Schaus, S.E.3
  • 28
    • 34249325209 scopus 로고    scopus 로고
    • Absolute stereochemistries of these new products were not determined by derivatization; however, by analogy to other aza-Henry products obtained using this methodology, we have assigned the stereochemistry as shown
    • Absolute stereochemistries of these new products were not determined by derivatization; however, by analogy to other aza-Henry products obtained using this methodology, we have assigned the stereochemistry as shown.
  • 29
    • 34249320223 scopus 로고    scopus 로고
    • 1H NMR correlation, see Supporting Information.
    • 1H NMR correlation, see Supporting Information.
  • 31
    • 20444441213 scopus 로고    scopus 로고
    • For the X-ray crystallographic structure of a derivative of catalyst la, see
    • For the X-ray crystallographic structure of a derivative of catalyst la, see: Xiao, Y.; Wang, Z.; Ding, K. Chem.-Eur. J. 2005, 11, 3668.
    • (2005) Chem.-Eur. J , vol.11 , pp. 3668
    • Xiao, Y.1    Wang, Z.2    Ding, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.