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Volumn , Issue 8, 2013, Pages 1558-1565

Catalytic asymmetric conjugate addition of α-substituted nitro acetates to nitro olefins: Enantioselective synthesis of highly substituted γ-lactams

Author keywords

Asymmetric catalysis; Conjugate addition; Lactams; Nitrogen heterocycles; Organocatalysis

Indexed keywords


EID: 84874898543     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201201444     Document Type: Conference Paper
Times cited : (23)

References (38)
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    • For catalytic enantioselective conjugate addition reactions of α-substituted nitro acetates to α,β-unsaturated bisphosphonates, see:, Y. Kato, Z. Chen, S. Matsunaga, M. Shibasaki, Synlett 2009, 1635-1638.
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  • 19
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    • For catalytic enantioselective conjugate addition reactions of α-substituted nitro acetates to α,β-unsaturated sulfones, see:, A. Quintard, A. Alexakis, Org. Biomol. Chem. 2011, 9, 1407-1418.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 1407-1418
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  • 20
    • 80052926575 scopus 로고    scopus 로고
    • For catalytic enantioselective conjugate addition reactions of α-substituted nitro acetates to maleimides, see:, S. Shirakawa, S. J. Terao, R. He, K. Maruoka, Chem. Commun. 2011, 47, 10557-10559.
    • (2011) Chem. Commun. , vol.47 , pp. 10557-10559
    • Shirakawa, S.1    Terao, S.J.2    He, R.3    Maruoka, K.4
  • 21
    • 11244281650 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 105 - 108
    • For catalytic enantioselective conjugate addition reactions of α-substituted nitro acetates to nitro olefins, see:, H. Li, Y. Wang, L. Tang, F. Wu, X. Liu, C. Guo, B. M. Foxman, L. Deng, Angew. Chem. 2005, 117, 107; Angew. Chem. Int. Ed. 2005, 44, 105-108.
    • (2005) Angew. Chem. , vol.117 , pp. 107
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  • 25
    • 34248185465 scopus 로고    scopus 로고
    • For catalytic asymmetric α-fluorination of α-substituted nitro acetates, see:, J. Ramírez, D. P. Huber, A. Togni, Synlett 2007, 1143-1147.
    • (2007) Synlett , pp. 1143-1147
    • Ramírez, J.1    Huber, D.P.2    Togni, A.3
  • 30
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    • Shimizu, M.1
  • 34
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    • For a recent review about an aromatic hydroxy group as a hydrogen-bonding activator in bifunctional asymmetric organocatalysis, see:, P. Chauhan, S. S. Chimni, RSC Adv. 2012, 2, 737-758.
    • (2012) RSC Adv. , vol.2 , pp. 737-758
    • Chauhan, P.1    Chimni, S.S.2
  • 35
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    • For a recent review, see:, A. Albrecht, Ł. Albrecht, T. Janecki, Eur. J. Org. Chem. 2011, 2747-2766, and references cited therein.
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    • Wiley-VCH, Weinheim, Germany
    • For the conversion of nitro compounds, see:, N. Ono, in: The Nitro Group in Organic Synthesis (Ed.:, N. Ono), Wiley-VCH, Weinheim, Germany, 2001, pp. 159-181.
    • (2001) The Nitro Group in Organic Synthesis , pp. 159-181
    • Ono, N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.