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Volumn 46, Issue 39, 2007, Pages 7356-7359

Radicals in asymmetric organocatalysis

Author keywords

Asymmetric catalysis; Carbonyl compounds; Enamines; Organocatalysis; Radicals

Indexed keywords

ACTIVATION ENERGY; AMINES; AMINO ACIDS; MOLECULAR ORBITALS;

EID: 35048898034     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200702834     Document Type: Review
Times cited : (57)

References (47)
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    • For recent reviews on organocatalysis, see: a
    • For recent reviews on organocatalysis, see: a) P. L. Dalko, L. Moisan, Angew. Chem. 2004, 116, 5248;
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    • Ed, P. I. Dalko, Wiley-VCH, Weinheim
    • c) Enantioselective Organocatalysis (Ed.: P. I. Dalko), Wiley-VCH, Weinheim, 2007;
    • (2007) Enantioselective Organocatalysis
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    • Enamine-SOMO activations were presented first on a number of conferences, see: D. W. C. MacMillan: March 31, 2006, Amgen (Thousand Oaks); April 27, 2006 (Manchester); June 13, 2006, IUPAC (Merida); July 25, 2006, IUPAC (Kyoto); September 11, 2006, ACS (San Francisco).
    • Enamine-SOMO activations were presented first on a number of conferences, see: D. W. C. MacMillan: March 31, 2006, Amgen (Thousand Oaks); April 27, 2006 (Manchester); June 13, 2006, IUPAC (Merida); July 25, 2006, IUPAC (Kyoto); September 11, 2006, ACS (San Francisco).
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    • 35048824726 scopus 로고    scopus 로고
    • For recent reviews on α-functionalizations using enamine activation, see: a
    • For recent reviews on α-functionalizations using enamine activation, see: a) M. Marigo, K. A. Jørgensen, Chem. Commun. 2006, 2001;
    • (2001) Chem. Commun , vol.2006
    • Marigo, M.1    Jørgensen, K.A.2
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    • 34250613134 scopus 로고    scopus 로고
    • For recent reviews on β-functionalizations using iminium-ion activation, see: a
    • For recent reviews on β-functionalizations using iminium-ion activation, see: a) S. B. Tsogoeva, Eur. J. Org. Chem. 2007, 1701;
    • (2007) Eur. J. Org. Chem , pp. 1701
    • Tsogoeva, S.B.1
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    • 35048899132 scopus 로고    scopus 로고
    • Melanin is believed to be the longest-existing free radical with a duration of millions of years
    • Melanin is believed to be the longest-existing free radical with a duration of millions of years
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    • For a review on radicals in enzymatic pathways, see
    • For a review on radicals in enzymatic pathways, see: P. A. Frey, A. D. Hegeman, G. H. Reed, Chem. Rev. 2006, 106, 3302.
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    • For highlights: f
    • For highlights: f) P. Wessig, Angew. Chem. 2006, 118, 224;
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    • Angew. Chem. Int. Ed. 2006, 45, 2168;
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    • TEMPO is a persistent radical known to perform coupling reactions with carbon-centered radicals; see: a D. L. Boger, J. A. McKie, J. Org. Chem. 1995, 60, 1271;
    • TEMPO is a persistent radical known to perform coupling reactions with carbon-centered radicals; see: a) D. L. Boger, J. A. McKie, J. Org. Chem. 1995, 60, 1271;
  • 45
  • 46


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.