메뉴 건너뛰기




Volumn 136, Issue 47, 2014, Pages 16515-16521

Copper(I)-catalyzed enantioselective synthesis of α-chiral linear or carbocyclic (e)-(γ-alkoxyallyl)boronates

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; COPPER; ENANTIOSELECTIVITY; FUNCTIONAL GROUPS; MATHEMATICAL TRANSFORMATIONS; MODULAR CONSTRUCTION; SYNTHESIS (CHEMICAL);

EID: 84914172540     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja506284w     Document Type: Article
Times cited : (71)

References (92)
  • 9
    • 22244490357 scopus 로고    scopus 로고
    • (for Ni-catalyzed reductive couplings of alkyne and α-oxyaldehyde)
    • Luanphaisarnnont, T.; Ndubaku, C. O.; Jamison, T. F. Org. Lett. 2005, 7, 2937 (for Ni-catalyzed reductive couplings of alkyne and α-oxyaldehyde)
    • (2005) Org. Lett. , vol.7 , pp. 2937
    • Luanphaisarnnont, T.1    Ndubaku, C.O.2    Jamison, T.F.3
  • 11
    • 1342285487 scopus 로고    scopus 로고
    • (for diastereoselective organozinc addition to α-oxyaldehydes)
    • Marshall, J. A.; Eidam, P. Org. Lett. 2004, 6, 445 (for diastereoselective organozinc addition to α-oxyaldehydes)
    • (2004) Org. Lett. , vol.6 , pp. 445
    • Marshall, J.A.1    Eidam, P.2
  • 14
    • 0035922327 scopus 로고    scopus 로고
    • (for (α-alkoxypropargyl)stannane addition to aldehydes)
    • Savall, B. M.; Powell, N. A.; Roush, W. R. Org. Lett. 2001, 3, 3057 (for (α-alkoxypropargyl)stannane addition to aldehydes)
    • (2001) Org. Lett. , vol.3 , pp. 3057
    • Savall, B.M.1    Powell, N.A.2    Roush, W.R.3
  • 20
    • 84873561013 scopus 로고    scopus 로고
    • For a review about the synthetic utility of allylic alcohols, see
    • For a review about the synthetic utility of allylic alcohols, see: Lumbroso, A.; Cooke, M. L.; Breit, B. Angew. Chem., Int. Ed. 2013, 52, 1890
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 1890
    • Lumbroso, A.1    Cooke, M.L.2    Breit, B.3
  • 21
    • 0002026625 scopus 로고    scopus 로고
    • Recent applications of the allylation reaction to the synthesis of natural products
    • Otera, J. Wiley-VCH: Weinheim, Germany
    • Chemler, S. R.; Roush, W. R. Recent applications of the allylation reaction to the synthesis of natural products. In Modern Carbonyl Chemistry; Otera, J., Ed.; Wiley-VCH: Weinheim, Germany, 2000; pp 403-490.
    • (2000) Modern Carbonyl Chemistry , pp. 403-490
    • Chemler, S.R.1    Roush, W.R.2
  • 22
    • 34447529397 scopus 로고    scopus 로고
    • Recent advances in the preparation of allylboronates and their use in tandem reactions with carbonyl compounds
    • Hall, D. G. Wiley-VCH: Weinheim, Germany.
    • Kennedy, J. W. J.; Hall, D. G. Recent advances in the preparation of allylboronates and their use in tandem reactions with carbonyl compounds. In Boronic Acids; Hall, D. G., Ed.; Wiley-VCH: Weinheim, Germany, 2005.
    • (2005) Boronic Acids
    • Kennedy, J.W.J.1    Hall, D.G.2
  • 72
    • 84858657097 scopus 로고    scopus 로고
    • Morken et al. reported on γ-selective boryl substitution of an allyl acetal containing a terminal alkene moiety using an achiral nickel(0) catalyst; see: Zhang, P.; Roundtree, I. A.; Morken, J. P. Org. Lett. 2012, 14, 1416
    • (2012) Org. Lett. , vol.14 , pp. 1416
    • Zhang, P.1    Roundtree, I.A.2    Morken, J.P.3
  • 81
    • 76349126369 scopus 로고    scopus 로고
    • For basic zinc(II)-catalyzed α-selective aldehyde allylation through transmetalation, see
    • For basic zinc(II)-catalyzed α-selective aldehyde allylation through transmetalation, see: Kobayashi, S.; Endo, T.; Schneider, U.; Ueno, M. Chem. Commun. 2010, 46, 1260
    • (2010) Chem. Commun. , vol.46 , pp. 1260
    • Kobayashi, S.1    Endo, T.2    Schneider, U.3    Ueno, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.