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Volumn 352, Issue 17, 2010, Pages 2875-2880

A recyclable organocascade reaction system: Stereoselective precipitation of optically active cis-δ-lactols with quaternary stereocenters during the Michael-hemiacetalization reaction

Author keywords

cascade reaction; green chemistry; hydrogen bonding; organocatalysis; quaternary stereocenters

Indexed keywords


EID: 78649588434     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201000553     Document Type: Article
Times cited : (15)

References (109)
  • 3
    • 55049138759 scopus 로고    scopus 로고
    • (Ed.: P.I. Dalko), Wiley-VCH, Weinheim
    • For reviews, see Enantioselective Organocatalysis, (Ed.:, P.I. Dalko,), Wiley-VCH, Weinheim, 2007
    • (2007) Enantioselective Organocatalysis
  • 4
    • 78649607814 scopus 로고    scopus 로고
    • special issue
    • B. List, (guest editor), Chem. Rev. 2007, 107, No. 12 (special issue)
    • (2007) Chem. Rev. , vol.107 , Issue.12
    • List, B.1
  • 7
    • 48849094479 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4638-4660
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4638-4660
  • 9
    • 53549121402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 6138-6171
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6138-6171
  • 12
    • 77950477105 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 2668-2679.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2668-2679
  • 15
    • 71949117774 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9608-9644
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9608-9644
  • 24
    • 33746216402 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 3093-3097
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3093-3097
  • 26
    • 34447285219 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 4329-4332
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4329-4332
  • 33
    • 0037021091 scopus 로고    scopus 로고
    • for examples, see
    • Angew. Chem. Int. Ed. 2002, 41, 3964-4000; for examples, see
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3964-4000
  • 35
  • 42
    • 67650094837 scopus 로고    scopus 로고
    • for some selected examples, see
    • For reviews, see M. Bella, T. Gasperi, Synthesis 2009, 1583-1614; for some selected examples, see
    • (2009) Synthesis , pp. 1583-1614
    • Bella, M.1    Gasperi, T.2
  • 49
    • 70349661720 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 7892-7894.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7892-7894
  • 54
    • 38349135345 scopus 로고    scopus 로고
    • for examples, see
    • For reviews, see A. G. Doyle, E. N. Jacobsen, Chem. Rev. 2007, 107, 5713-5743; for examples, see
    • (2007) Chem. Rev. , vol.107 , pp. 5713-5743
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 62
    • 68149151038 scopus 로고    scopus 로고
    • for examples, see
    • For reviews, see O. N. Burchak, S. Py, Tetrahedron 2009, 65, 7333-7356; for examples, see
    • (2009) Tetrahedron , vol.65 , pp. 7333-7356
    • Burchak, O.N.1    Py, S.2
  • 67
    • 33947198541 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1570-1581
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1570-1581
  • 68
    • 44949242294 scopus 로고    scopus 로고
    • for selected examples of secondary-amine-catalyzed cascade reactions, see
    • X. Yu, W. Wang, Org. Biomol. Chem. 2008, 6, 2037-2046; for selected examples of secondary-amine-catalyzed cascade reactions, see
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 2037-2046
    • Yu, X.1    Wang, W.2
  • 70
  • 74
    • 23744473863 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4877-4880
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4877-4880
  • 80
    • 34248192461 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 1101-1104
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1101-1104
  • 83
    • 53549126884 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 3046-3049
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3046-3049
  • 88
    • 70349777755 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3699-3702
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3699-3702
  • 90
    • 70349897776 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5701-5704
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5701-5704
  • 92
    • 72449151738 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9834-9838
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9834-9838
  • 103
    • 78649547658 scopus 로고    scopus 로고
    • CCDC 771632 (5) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 771632 (5) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
  • 104
    • 78649561579 scopus 로고    scopus 로고
    • For recent reviews on non-linear effects, see
    • For recent reviews on non-linear effects, see
  • 108
  • 109
    • 73949140284 scopus 로고    scopus 로고
    • For a similar explanation, see
    • For a similar explanation, see:, I. Fleischer, A. Pfaltz, Chem. Eur. J. 2010, 16, 95-99.
    • (2010) Chem. Eur. J. , vol.16 , pp. 95-99
    • Fleischer, I.1    Pfaltz, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.