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Volumn 2014, Issue 1, 2014, Pages 152-163

Enantioselective organocatalytic synthesis of α- cyclopropylphosphonates through a domino michael addition/intramolecular alkylation reaction

Author keywords

Aldehydes; Cyclopropanes; Domino reactions; Michael addition; Organocatalysis

Indexed keywords


EID: 84890780833     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201301207     Document Type: Article
Times cited : (10)

References (86)
  • 4
    • 84890760692 scopus 로고    scopus 로고
    • Cyclopropyl Group
    • (Ed.:, Z. Rappport), Wiley, Chichester, UK
    • B. Rozsondai, Cyclopropyl Group, in: Patai's Chemistry of Functional Groups (Ed.:, Z. Rappport), Wiley, Chichester, UK, 2004, vol. 2, p. 1-83.
    • (2004) Patai's Chemistry of Functional Groups , vol.2 , pp. 1-83
    • Rozsondai, B.1
  • 10
    • 83455214076 scopus 로고    scopus 로고
    • for recent reviews on organocatalytic enantioselective synthesis of phosphonates, see
    • A. M. Faísca Phillips, M. T. Barros, Org. Biomol. Chem. 2012, 10, 404-412; for recent reviews on organocatalytic enantioselective synthesis of phosphonates, see
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 404-412
    • Faísca Phillips, A.M.1    Barros, M.T.2
  • 12
    • 73949085623 scopus 로고    scopus 로고
    • for organocatalytic asymmetric synthesis of organophosphorus compounds, see: Ł. Albrecht
    • for organocatalytic asymmetric synthesis of organophosphorus compounds, see: Ł. Albrecht, A. Albrecht, H. Krawczyk, K. A. Jorgensen, Chem. Eur. J. 2010, 16, 28-48.
    • (2010) Chem. Eur. J. , vol.16 , pp. 28-48
    • Albrecht, A.1    Krawczyk, H.2    Jorgensen, K.A.3
  • 31
    • 33947198541 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1570-1581.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1570-1581
  • 37
    • 4544374715 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 2681-2684.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2681-2684
  • 39
    • 5344280509 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 4641-4644.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 4641-4644
  • 41
    • 33748765777 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6024-6028; for intermolecular cyclopropane synthesis from enones, see
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 6024-6028
  • 49
    • 34547098110 scopus 로고    scopus 로고
    • A. Hartikka, P. I. Arvidsson, J. Org. Chem. 2007, 72, 5874-5877; for synthesis from α,γ-unsaturated aldehydes and arsonium-ylides, see
    • (2007) J. Org. Chem. , vol.72 , pp. 5874-5877
    • Hartikka, A.1    Arvidsson, P.I.2
  • 60
    • 84860386125 scopus 로고    scopus 로고
    • for cyclopropanation through oxidative N-heterocyclic carbene catalysis, see
    • for cyclopropanation through oxidative N-heterocyclic carbene catalysis, see, A. Biswas, S. De Sarkar, L. Tebben, A. Studer, Chem. Commun. 2012, 48, 5190-5192.
    • (2012) Chem. Commun. , vol.48 , pp. 5190-5192
    • Biswas, A.1    De Sarkar, S.2    Tebben, L.3    Studer, A.4
  • 82
    • 84890728083 scopus 로고    scopus 로고
    • for a recent review on the determination of enantiomeric excesses by NMR spectroscopy, see
    • for a recent review on the determination of enantiomeric excesses by NMR spectroscopy, see:, T. J. Wenzel, J. D. Wilcox, Chirality 2003, 15, 3469-3472.
    • (2003) Chirality , vol.15 , pp. 3469-3472
    • Wenzel, T.J.1    Wilcox, J.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.