메뉴 건너뛰기




Volumn 46, Issue 6, 2010, Pages 904-906

Diastereoselective and enantioselective Mukaiyama aldol reactions of α-ketoesters using hydrogen bond catalysis

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; ALCOHOL DERIVATIVE; ALPHA KETOESTER; ESTER DERIVATIVE; KETONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 75649088899     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b919929b     Document Type: Article
Times cited : (46)

References (44)
  • 2
    • 84889375944 scopus 로고    scopus 로고
    • J. Christoffers and A. Baro, Wiley-VCH, Weinheim, Germany, For reviews of recent developments on the creation of chiral tertiary alcohols by nucleophilic additions to ketone carbonyls, see
    • For reviews of recent developments on the creation of chiral tertiary alcohols by nucleophilic additions to ketone carbonyls, see: Quaternary Stereocenters: Challenges and Solutions for Organic Synthesis, ed., J. Christoffers, and, A. Baro, Wiley-VCH, Weinheim, Germany, 2005
    • (2005) Quaternary Stereocenters: Challenges and Solutions for Organic Synthesis, Ed.
  • 4
    • 0037165679 scopus 로고    scopus 로고
    • Enantioselective Mukaiyama aldol reactions of ketones
    • Enantioselective Mukaiyama aldol reactions of ketones: S. E. Denmark Y. Fan J. Am. Chem. Soc. 2002 124 4233 4234
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 4233-4234
    • Denmark, S.E.1    Fan, Y.2
  • 7
    • 0030580328 scopus 로고    scopus 로고
    • For examples of diastereoselective pyruvate aldol reactions, see
    • For examples of diastereoselective pyruvate aldol reactions, see: I. C. Jacobson G. P. Reddy Tetrahedron Lett. 1996 37 8263 8266
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8263-8266
    • Jacobson, I.C.1    Reddy, G.P.2
  • 11
    • 0004764938 scopus 로고
    • Enantioselective pyruvate aldol reactions promoted by stoichiometric chiral metal complexes
    • Enantioselective pyruvate aldol reactions promoted by stoichiometric chiral metal complexes: S. Kobayashi I. Hachiya J. Org. Chem. 1992 57 1324 1328
    • (1992) J. Org. Chem. , vol.57 , pp. 1324-1328
    • Kobayashi, S.1    Hachiya, I.2
  • 13
    • 9244221087 scopus 로고    scopus 로고
    • Enantioselective pyruvate Mukaiyama aldol reactions promoted by substoichiometric metal complexes
    • Enantioselective pyruvate Mukaiyama aldol reactions promoted by substoichiometric metal complexes: M. Langner C. Bolm Angew. Chem., Int. Ed. 2004 43 5984 5987
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 5984-5987
    • Langner, M.1    Bolm, C.2
  • 17
    • 71549172794 scopus 로고    scopus 로고
    • After this work had been accepted for publication, an additional example of Lewis acid catalyzed enantioselective Mukaiyama aldol reaction of α-ketoesters appeared in press:
    • After this work had been accepted for publication, an additional example of Lewis acid catalyzed enantioselective Mukaiyama aldol reaction of α-ketoesters appeared in press: J. Le Engers B. L. Pagenkopf Eur. J. Org. Chem. 2009 6109 6111
    • (2009) Eur. J. Org. Chem. , pp. 6109-6111
    • Le Engers, J.1    Pagenkopf, B.L.2
  • 18
    • 33845196489 scopus 로고    scopus 로고
    • For representative examples of natural products containing this motif, see: footnote 5 in reference 7(c) Kinamycins:
    • For representative examples of natural products containing this motif, see: footnote 5 in reference 7(c) Kinamycins: X. Lei J. A. Porco, Jr. J. Am. Chem. Soc. 2006 128 14790 14791
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 14790-14791
    • Lei, X.1    Porco, Jr.J.A.2
  • 25
  • 29
    • 53549096325 scopus 로고    scopus 로고
    • P. I. Dalko, Wiley-VCH, Weinheim Recent reviews on enantioselective reactions catalyzed by chiral hydrogen bond donors
    • Recent reviews on enantioselective reactions catalyzed by chiral hydrogen bond donors: J. D. McGilvra, V. B. Gondi and V. H. Rawal, in Enantioselective organocatalysis, ed., P. I. Dalko, Wiley-VCH, Weinheim, 2007, pp. 189-254
    • (2007) Enantioselective Organocatalysis, Ed. , pp. 189-254
    • McGilvra, J.D.1    Gondi, V.B.2    Rawal, V.H.3
  • 33
    • 0000714570 scopus 로고    scopus 로고
    • For selected examples of hydrogen bond catalyzed asymmetric reactions of ketones from other labs, see
    • For selected examples of hydrogen bond catalyzed asymmetric reactions of ketones from other labs, see: T. Schuster M. Bauch G. Düerner M. W. Göebel Org. Lett. 2000 2 179 181
    • (2000) Org. Lett. , vol.2 , pp. 179-181
    • Schuster, T.1    Bauch, M.2    Düerner, G.3    Göebel, M.W.4
  • 37
    • 0242432417 scopus 로고    scopus 로고
    • Prior work from this lab on hydrogen bond catalyzed asymmetric reactions of carbonyl electrophiles
    • Prior work from this lab on hydrogen bond catalyzed asymmetric reactions of carbonyl electrophiles: Y. Huang A. K. Unni A. N. Thadani V. H. Rawal Nature 2003 424 146 146
    • (2003) Nature , vol.424 , pp. 146-146
    • Huang, Y.1    Unni, A.K.2    Thadani, A.N.3    Rawal, V.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.