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Volumn 17, Issue 50, 2011, Pages 14267-14272

Microwave-assisted organocatalytic enantioselective intramolecular aza-Michael reaction with α,β-unsaturated ketones

Author keywords

aza Michael reaction; cinchona alkaloids; heterocycles; microwave chemistry; organocatalysis

Indexed keywords

AZA-MICHAEL REACTION; CINCHONA ALKALOID; HETEROCYCLES; MICROWAVE CHEMISTRY; ORGANOCATALYSIS;

EID: 82955174898     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201101292     Document Type: Article
Times cited : (51)

References (89)
  • 36
    • 0037070622 scopus 로고    scopus 로고
    • for examples with hydrazones as nitrogen nucleophiles, see
    • D. J. Guerin, S. J. Miller, J. Am. Chem. Soc. 2002, 124, 2134; for examples with hydrazones as nitrogen nucleophiles, see
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2134
    • Guerin, D.J.1    Miller, S.J.2
  • 37
    • 34247597207 scopus 로고    scopus 로고
    • for examples with nitrogen heterocycles as nucleophiles, see
    • D. Perdicchia, K. A. Jørgensen, J. Org. Chem. 2007, 72, 3565; for examples with nitrogen heterocycles as nucleophiles, see
    • (2007) J. Org. Chem. , vol.72 , pp. 3565
    • Perdicchia, D.1    Jørgensen, K.A.2
  • 45
    • 33644619459 scopus 로고    scopus 로고
    • The first reported participation of enones in an aminocatalyzed aza-Michael reaction dates from 2005
    • The first reported participation of enones in an aminocatalyzed aza-Michael reaction dates from 2005:, H. Sundén, I. Ibrahem, L. Eriksson, A. Cõrdova, Angew. Chem. 2005, 117, 4955
    • (2005) Angew. Chem. , vol.117 , pp. 4955
    • Sundén, H.1    Ibrahem, I.2    Eriksson, L.3    Cõrdova, A.4
  • 46
    • 23744473863 scopus 로고    scopus 로고
    • These authors reported a highly enantioselective proline-catalyzed aza-Diels-Alder reaction proceeding through a tandem Mannich-intramolecular aza-Michael reaction pathway.
    • Angew. Chem. Int. Ed. 2005, 44, 4877. These authors reported a highly enantioselective proline-catalyzed aza-Diels-Alder reaction proceeding through a tandem Mannich-intramolecular aza-Michael reaction pathway.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4877
  • 56
    • 44949251617 scopus 로고    scopus 로고
    • For 9-amino cinchona alkaloid-catalyzed intermolecular aza-Michael reactions, see
    • L.-W. Xu, Y. Lu, Org. Biomol. Chem. 2008, 6, 2047. For 9-amino cinchona alkaloid-catalyzed intermolecular aza-Michael reactions, see
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 2047
    • Xu, L.-W.1    Lu, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.