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Volumn , Issue , 2009, Pages 141-351

(Thio)urea Organocatalysts

Author keywords

Claisen rearrangement; Diels Alder reactions; Friedel Crafts alkylation; Host guest complexes; Metal free catalysis; Michaelis Menten kinetics; Morita Baylis Hillman reaction; Thiourea organocatalysts

Indexed keywords


EID: 84891543496     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527627844.ch6     Document Type: Chapter
Times cited : (85)

References (352)
  • 10
    • 33748632360 scopus 로고    scopus 로고
    • Carey, P.R. (2006) Chem. Rev., 106, 3043-3054.
    • (2006) Chem. Rev. , vol.106 , pp. 3043-3054
    • Carey, P.R.1
  • 13
    • 33748608826 scopus 로고    scopus 로고
    • Bruice, T.C. (2006) Chem. Rev., 106, 3119-3139.
    • (2006) Chem. Rev. , vol.106 , pp. 3119-3139
    • Bruice, T.C.1
  • 15
    • 0003438540 scopus 로고
    • The Nature of the Chemical Bond
    • 3rd edn, Cornell University Press, Ithaca
    • Pauling, L. (1968) The Nature of the Chemical Bond, 3rd edn, Cornell University Press, Ithaca.
    • (1968)
    • Pauling, L.1
  • 16
    • 0010302962 scopus 로고
    • The Hydrogen Bond, Freeman
    • San Francisco
    • Pimentel, G.C. and McClellan, A.L. (1960) The Hydrogen Bond, Freeman, San Francisco.
    • (1960)
    • Pimentel, G.C.1    McClellan, A.L.2
  • 17
    • 0003914038 scopus 로고    scopus 로고
    • An Introduction to Hydrogen Bonding
    • Oxford University Press, New York
    • Jeffrey, G.A. (1997) An Introduction to Hydrogen Bonding, Oxford University Press, New York.
    • (1997)
    • Jeffrey, G.A.1
  • 36
    • 0004166052 scopus 로고    scopus 로고
    • Comprehensive Biological Catalysis
    • Academic Press, London
    • Wharton, C.W. (1998) Comprehensive Biological Catalysis, Vol. 1, Academic Press, London.
    • (1998) , vol.1
    • Wharton, C.W.1
  • 37
    • 84889432812 scopus 로고    scopus 로고
    • Multi-Step Enzyme Catalysis
    • Product inhibition and substrate inhibition are effects also known in enzyme catalysis that can reduce catalytic efficiency. Generally, catalytic systems (natural or artificial) based on covalent interactions are more sensitive towards inhibitions than non-covalent systems utilizing weak interactions, Wiley-VCH Verlag GmbH, Weinheim, Germany
    • Product inhibition and substrate inhibition are effects also known in enzyme catalysis that can reduce catalytic efficiency. Generally, catalytic systems (natural or artificial) based on covalent interactions are more sensitive towards inhibitions than non-covalent systems utilizing weak interactions: Garcia-Junceda, E. (2008) Multi-Step Enzyme Catalysis, Wiley-VCH Verlag GmbH, Weinheim, Germany.
    • (2008)
    • Garcia-Junceda, E.1
  • 40
    • 0019915836 scopus 로고
    • Breslow, R. (1982) Science, 218, 532-537.
    • (1982) Science , vol.218 , pp. 532-537
    • Breslow, R.1
  • 41
    • 84891017895 scopus 로고    scopus 로고
    • Artificial Enzymes
    • Wiley-VCH Verlag GmbH, Weinheim
    • Breslow, R. (2005) Artificial Enzymes, Wiley-VCH Verlag GmbH, Weinheim.
    • (2005)
    • Breslow, R.1
  • 44
    • 0000421878 scopus 로고
    • Pauling, L. (1948) Nature, 161, 707-709.
    • (1948) Nature , vol.161 , pp. 707-709
    • Pauling, L.1
  • 47
    • 38349189109 scopus 로고    scopus 로고
    • Akiyama, T. (2007) Chem. Rev., 107, 5744-5758.
    • (2007) Chem. Rev. , vol.107 , pp. 5744-5758
    • Akiyama, T.1
  • 59
    • 47749122232 scopus 로고    scopus 로고
    • Asymmetric Organocatalysis
    • Wiley-VCH Verlag GmbH, Weinheim, Germany
    • Berkessel, A. and Gröger, H. (2005) Asymmetric Organocatalysis, Wiley-VCH Verlag GmbH, Weinheim, Germany.
    • (2005)
    • Berkessel, A.1    Gröger, H.2
  • 66
    • 55049138759 scopus 로고    scopus 로고
    • Enantioselective Organocatalysis-Reactions and Experimental Procedures
    • Wiley-VCH Verlag GmbH, Weinheim, Germany
    • Dalko, P.I. (2007) Enantioselective Organocatalysis-Reactions and Experimental Procedures, Wiley-VCH Verlag GmbH, Weinheim, Germany.
    • (2007)
    • Dalko, P.I.1
  • 83
  • 84
    • 14744286984 scopus 로고    scopus 로고
    • Various authors
    • Various authors (2004) Organic catalysis. Adv. Synth. Catal., 346 (9-10), 1007-1249.
    • (2004) Organic catalysis. Adv. Synth. Catal. , vol.346 , Issue.9-10 , pp. 1007-1249
  • 88
    • 0001686851 scopus 로고
    • Hine, J., Ahn, K., Gallucci, J.C. and Linden, S.-M. (1984) J. Am. Chem. Soc., 106, 7980-7981.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 7980-7981
  • 89
    • 37049092261 scopus 로고
    • A crystal structure of an unstable N, N '-[bis-(á-tosylbenzyl)urea-acetone hydrogen-bonded adduct had been reported earlier
    • A crystal structure of an unstable N, N '-[bis-(á-tosylbenzyl)urea-acetone hydrogen-bonded adduct had been reported earlier: Tel, R M. and Engberts, J.B.F.N. (1976). J. Chem. Soc. Perkin Trans. 2, 483-488.
    • (1976) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 483-488
    • Tel, R.M.1    Engberts, J.B.F.N.2
  • 111
    • 84891541324 scopus 로고    scopus 로고
    • Diploma Thesis
    • University of Göttingen, Germany
    • Wittkopp, A. (1997) Diploma Thesis. University of Göttingen, Germany.
    • (1997)
    • Wittkopp, A.1
  • 116
    • 0000252506 scopus 로고    scopus 로고
    • The Chemistry of Dienes and Polyenes
    • (ed. Z. Rappoport), John Wiley & Sons, Ltd, Chichester
    • Wittkopp, A. and Schreiner, P.R. (2000) The Chemistry of Dienes and Polyenes, Vol. 2 (ed. Z. Rappoport), John Wiley & Sons, Ltd, Chichester, pp. 1029-1088.
    • (2000) , vol.2 , pp. 1029-1088
    • Wittkopp, A.1    Schreiner, P.R.2
  • 117
    • 84891543700 scopus 로고
    • Ostwald, W. (1910) Chem. Z., 34, 397-399.
    • (1910) Chem. Z. , vol.34 , pp. 397-399
    • Ostwald, W.1
  • 122
    • 84891522201 scopus 로고    scopus 로고
    • Dissertation, University Giessen
    • forthcoming, University of Giessen, Germany; online access via the Electronic Library
    • Kotke, M. (forthcoming) Dissertation, University Giessen, University of Giessen, Germany; online access via the Electronic Library.
    • Kotke, M.1
  • 127
    • 84891499626 scopus 로고    scopus 로고
    • Dissertation, University of Göttingen
    • Germany, published online
    • Wittkopp, A. (2001) Dissertation, University of Göttingen, Germany, published online.
    • (2001)
    • Wittkopp, A.1
  • 129
    • 0003980673 scopus 로고    scopus 로고
    • Green Chemistry: Theory and Practice
    • Oxford University Press, Oxford, UK
    • Anastas, P.T. and Warner, J.C. (1998) Green Chemistry: Theory and Practice, Oxford University Press, Oxford, UK.
    • (1998)
    • Anastas, P.T.1    Warner, J.C.2
  • 141
    • 3042961533 scopus 로고
    • Die organischen Katalysatoren und ihre Beziehungen zu den Fermenten (Organic Catalysts and their Relation to the Enzymes)
    • 2nd edn, Springer, Berlin
    • Langenbeck, W. (1949) Die organischen Katalysatoren und ihre Beziehungen zu den Fermenten (Organic Catalysts and their Relation to the Enzymes), 2nd edn, Springer, Berlin.
    • (1949)
    • Langenbeck, W.1
  • 160
    • 0004152486 scopus 로고    scopus 로고
    • Water-A Matrix of Life
    • 2nd edn, Royal Society of Chemistry, Cambridge, UK
    • Franks, F. (2000) Water-A Matrix of Life, 2nd edn, Royal Society of Chemistry, Cambridge, UK.
    • (2000)
    • Franks, F.1
  • 163
    • 0041378065 scopus 로고    scopus 로고
    • Gröger, H. (2003) Chem. Rev., 103, 2795-2827.
    • (2003) Chem. Rev. , vol.103 , pp. 2795-2827
    • Gröger, H.1
  • 171
    • 54149111407 scopus 로고    scopus 로고
    • Huang, Y. (2007) Synlett, 14, 2304-2305.
    • (2007) Synlett , vol.14 , pp. 2304-2305
    • Huang, Y.1
  • 192
    • 0001595852 scopus 로고
    • Otera, J. (1993) Chem. Rev., 93, 1449-1470.
    • (1993) Chem. Rev. , vol.93 , pp. 1449-1470
    • Otera, J.1
  • 203
    • 77952107224 scopus 로고
    • Organic Synthesis Collective
    • HCN was generated by the method of Ziegler. Alternatively, the generation of HCN in situ by reaction of TMSCN and MeOH afforded identical results, (eds H. Gilman and A.H. Blatt), John Wiley & Sons, Inc., New York
    • HCN was generated by the method of Ziegler. Alternatively, the generation of HCN in situ by reaction of TMSCN and MeOH afforded identical results. Ziegler, K. (1932) Organic Synthesis Collective, Volume 1 (eds H. Gilman and A.H. Blatt), John Wiley & Sons, Inc., New York, p. 314.
    • (1932) , vol.1 , pp. 314
    • Ziegler, K.1
  • 250
    • 0001280431 scopus 로고    scopus 로고
    • Both enantiomers of trans-1,2- aminocyclohexanephosphine were readily accessed on a multi-gram scale using a modification of the literature procedure
    • Both enantiomers of trans-1,2- aminocyclohexanephosphine were readily accessed on a multi-gram scale using a modification of the literature procedure: Caiazzo, A., Dalili, S. and Yudin, A.K. (2002) Org. Lett., 4, 2597-2600.
    • (2002) Org. Lett. , vol.4 , pp. 2597-2600
    • Caiazzo, A.1    Dalili, S.2    Yudin, A.K.3
  • 275
    • 49649083136 scopus 로고    scopus 로고
    • Chen, Y.-C. (2008) Synlett, 13, 1919-1930.
    • (2008) Synlett , vol.13 , pp. 1919-1930
    • Chen, Y.-C.1


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