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Volumn 16, Issue 26, 2010, Pages 7714-7718

Organocatalytic asymmetric cyanosilylation of nitroalkenes

Author keywords

Asymmetric catalysis; Bifunctional catalysis; Conjugate addition; Nitroalkenes; Organocatalysis; Synthetic methods

Indexed keywords

ASYMMETRIC CATALYSIS; BIFUNCTIONAL CATALYSIS; CONJUGATE ADDITION; NITROALKENES; ORGANOCATALYSIS; SYNTHETIC METHODS;

EID: 77954340277     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001107     Document Type: Article
Times cited : (91)

References (25)
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    • For a recent review on the activation of TMSCN by bases, see
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  • 11
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    • For reviews concerning bifunctional thiourea organocatalysis, see: a
    • For reviews concerning bifunctional thiourea organocatalysis, see: a) A.G. Doyle, E.N. Jacobsen, Chem. Rev. 2007, 107, 5713-5743;
    • (2007) Chem. Rev. , vol.107 , pp. 5713-5743
    • Doyle, A.G.1    Jacobsen, E.N.2
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    • Angew. Chem. Int. Ed. 2006, 45, 1520-1543;
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 1520-1543
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    • Angew. Chem. Int. Ed. 2006, 45, 7606-7608.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7606-7608
  • 22
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    • Reactions of 7 with conventional, alkylating reagents resulted in the undesired alkylation of the thiourea sulfur atom.
    • Reactions of 7 with conventional, alkylating reagents resulted in the undesired alkylation of the thiourea sulfur atom.
  • 23
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    • The reaction using β-nitrostyrene as representative of aromatic substrates was unsuccessfully investigated.
    • The reaction using β-nitrostyrene as representative of aromatic substrates was unsuccessfully investigated.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.