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Volumn 50, Issue 41, 2011, Pages 9680-9683

Direct asymmetric α benzoyloxylation of cyclic ketones

Author keywords

asymmetric catalysis; ketones; organocatalysis; oxidation; synthetic methods

Indexed keywords

ASYMMETRIC CATALYSIS; BENZOYL PEROXIDE; CYCLIC KETONES; ENANTIOSELECTIVE; ORGANOCATALYSIS; OXYGEN SOURCES; PRIMARY AMINES; SYNTHETIC METHODS;

EID: 80053523826     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201104244     Document Type: Article
Times cited : (68)

References (51)
  • 6
    • 77649206387 scopus 로고    scopus 로고
    • For recent reviews of organocatalyzed asymmetric α oxygenation of carbonyls, see: T. Vilaivan, W. Bhanthumnavin, Molecules 2010, 15, 917
    • (2010) Molecules , vol.15 , pp. 917
    • Vilaivan, T.1    Bhanthumnavin, W.2
  • 20
    • 70449449836 scopus 로고    scopus 로고
    • A single report describes a stoichiometric use of the carbonyl reagent using nitrosotoluene:, Reaction-specific optimization and higher catalyst loading to achieve a method stoichiometric in aldehyde has also been employed two steps into a total synthesis
    • A single report describes a stoichiometric use of the carbonyl reagent using nitrosotoluene:, P. Jiao, H. Yamamoto, Synlett 2009, 2685. Reaction-specific optimization and higher catalyst loading to achieve a method stoichiometric in aldehyde has also been employed two steps into a total synthesis
    • (2009) Synlett , pp. 2685
    • Jiao, P.1    Yamamoto, H.2
  • 27
    • 79960265175 scopus 로고    scopus 로고
    • also see: benzoyloxylation of oxindoles using a calcium phosphate catalyst
    • also see: benzoyloxylation of oxindoles using a calcium phosphate catalyst:, Z. Zhang, W. Zheng, J. C. Antilla, Angew. Chem. 2011, 123, 1167
    • (2011) Angew. Chem. , vol.123 , pp. 1167
    • Zhang, Z.1    Zheng, W.2    Antilla, J.C.3
  • 35
    • 79959992875 scopus 로고    scopus 로고
    • To the best of our knowledge, there are no reports on the use of primary amine catalysis for the enantioselective α oxygenation of carbonyl compounds. A recent publication describing the use of a primary amine catalyst in the reaction between α-unbranched aldehydes and nitrosobenzene reports exclusive N selectivity.
    • To the best of our knowledge, there are no reports on the use of primary amine catalysis for the enantioselective α oxygenation of carbonyl compounds. A recent publication describing the use of a primary amine catalyst in the reaction between α-unbranched aldehydes and nitrosobenzene reports exclusive N selectivity:, L. Qin, L. Li, L. Yi, C.-S. Da, Y.-F. Zhou, Chirality 2011, 23, 527.
    • (2011) Chirality , vol.23 , pp. 527
    • Qin, L.1    Li, L.2    Yi, L.3    Da, C.-S.4    Zhou, Y.-F.5
  • 38
    • 67549137639 scopus 로고    scopus 로고
    • For a review of cinchona-derived primary amines in organocatalysis, see
    • L.-W. Xu, J. Luoa, Y. Lu, Chem. Commun. 2009, 1807. For a review of cinchona-derived primary amines in organocatalysis, see
    • (2009) Chem. Commun. , pp. 1807
    • Xu, L.-W.1    Luoa, J.2    Lu, Y.3
  • 39
    • 49649083136 scopus 로고    scopus 로고
    • For selected examples of enamine catalysis by primary cinchona-alkaloid-derived amines, see
    • Y.-C. Chen, Synlett 2008, 1919. For selected examples of enamine catalysis by primary cinchona-alkaloid-derived amines, see
    • (2008) Synlett , pp. 1919
    • Chen, Y.-C.1
  • 48
    • 33344454722 scopus 로고    scopus 로고
    • For a synthesis of α-hydroxylcholestanone using nitrosobenzene and proline catalysis, see.
    • For a synthesis of α-hydroxylcholestanone using nitrosobenzene and proline catalysis, see:, S. A. Snyder, E. J. Corey, Tetrahedron Lett. 2006, 47, 2083.
    • (2006) Tetrahedron Lett. , vol.47 , pp. 2083
    • Snyder, S.A.1    Corey, E.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.