메뉴 건너뛰기




Volumn 52, Issue 1, 2013, Pages 441-445

Enantioselective decarboxylative amination: Synthesis of axially chiral allenyl amines

Author keywords

Allene; Amination; Chirality; Enantioselectivity; Synthetic methods

Indexed keywords

ALLENE; ALLENYL; CHIRAL LIGAND; ENANTIOSELECTIVE; PALLADIUM-CATALYZED; SYNTHETIC METHODS;

EID: 84871945650     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201204796     Document Type: Article
Times cited : (80)

References (66)
  • 1
    • 22944485617 scopus 로고    scopus 로고
    • For recent reviews on the chemistry of allenes
    • For recent reviews on the chemistry of allenes, see: a) S. Ma, Chem. Rev. 2005, 105, 2829
    • (2005) Chem. Rev. , vol.105 , pp. 2829
    • Ma, S.1
  • 11
    • 0038301132 scopus 로고    scopus 로고
    • For reviews on the synthesis of allenes
    • For reviews on the synthesis of allenes, see: a) L. K. Sydnes, Chem. Rev. 2003, 103, 1133
    • (2003) Chem. Rev. , vol.103 , pp. 1133
    • Sydnes, L.K.1
  • 12
    • 4544320494 scopus 로고    scopus 로고
    • (Eds.: N. Krause, A. S. K. Hashmi), Wiley-VCH, Weinheim
    • Modern Allene Chemistry, Vol. 1 and 2 (Eds.: N. Krause, A. S. K. Hashmi), Wiley-VCH, Weinheim, 2004
    • (2004) Modern Allene Chemistry , vol.1-2
  • 18
    • 0141765945 scopus 로고    scopus 로고
    • For recent reviews on the chemistry of allenes involving chirality transfer
    • For recent reviews on the chemistry of allenes involving chirality transfer, S. Ma, Acc. Chem. Res. 2003, 36, 701
    • (2003) Acc. Chem. Res. , vol.36 , pp. 701
    • Ma, S.1
  • 39
    • 0035820019 scopus 로고    scopus 로고
    • For the synthesis of chiral allenes via an α-methylene π-allylpalladium intermediate using malonates as the nucleophiles
    • For the synthesis of chiral allenes via an α-methylene π-allylpalladium intermediate using malonates as the nucleophiles, M. Ogasawara, H. Ikeda, T. Nagano, T. Hayashi, J. Am. Chem. Soc. 2001, 123, 2089
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 2089
    • Ogasawara, M.1    Ikeda, H.2    Nagano, T.3    Hayashi, T.4
  • 49
    • 79952688980 scopus 로고    scopus 로고
    • For review on decarboxylative allylation reactions
    • For review on decarboxylative allylation reactions, see: J. D. Weaver, A. Recio III, A. J. Grenning, J. A. Tunge, Chem. Rev. 2011, 111, 1846, and references therein.
    • (2011) Chem. Rev. , vol.111 , pp. 1846
    • Weaver, J.D.1    Recio Iii, A.2    Grenning, A.J.3    Tunge, J.A.4
  • 50
    • 31444438679 scopus 로고    scopus 로고
    • For some reports on the enantioselective allylation using chiral binap
    • For some reports on the enantioselective allylation using chiral binap, N. Kinoshita, T. Kawabata, K. Tsubaki, M. Bando, K. Fuji, Tetrahedron 2006, 62, 1756
    • (2006) Tetrahedron , vol.62 , pp. 1756
    • Kinoshita, N.1    Kawabata, T.2    Tsubaki, K.3    Bando, M.4    Fuji, K.5
  • 55
    • 6844254916 scopus 로고    scopus 로고
    • For some reviews on enantioselective allylation using the Trost ligand
    • For some reviews on enantioselective allylation using the Trost ligand, B. M. Trost, D. L. van Vranken, Chem. Rev. 1996, 96, 395
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 58
    • 84871969289 scopus 로고    scopus 로고
    • int = 0.0452), number of observations [ > 2σ(I)] 5779, parameters: 487. CCDC 885180 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • int = 0.0452), number of observations [ > 2σ(I)] 5779, parameters: 487. CCDC 885180 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.