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Volumn 51, Issue 49, 2012, Pages 12330-12333

N-Heterocyclic-carbene-catalyzed asymmetric oxidative hetero-diels-alder reactions with simple aliphatic aldehydes

Author keywords

asymmetric catalysis; cycloaddition; lactams; N heterocyclic carbene; oxidation

Indexed keywords

ALIPHATIC ALDEHYDES; ASYMMETRIC CATALYSIS; ENANTIOSELECTIVE APPROACH; ENOLATE INTERMEDIATES; HETERO-DIELS-ALDER REACTIONS; LACTAMS; N-HETEROCYCLIC CARBENES;

EID: 84870485888     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201206490     Document Type: Article
Times cited : (158)

References (61)
  • 19
    • 84870564957 scopus 로고    scopus 로고
    • T.-Y. Jian, P.-L. Shao, S. Ye
    • T.-Y. Jian, P.-L. Shao, S. Ye
  • 20
    • 79751470981 scopus 로고    scopus 로고
    • Chem. Commun. 2011, 47, 2381-2383
    • (2011) Chem. Commun. , vol.47 , pp. 2381-2383
  • 32
    • 78649563244 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 9266-9269
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9266-9269
  • 35
    • 84861633806 scopus 로고    scopus 로고
    • Chi and co-workers has recently demonstrated an oxidative approach to converting β-methyl enals into dienolate/azolium intermediates and their subsequent conversion into -lactones. See
    • Chi and co-workers has recently demonstrated an oxidative approach to converting β-methyl enals into dienolate/azolium intermediates and their subsequent conversion into -lactones. See:, J. Mo, X. Chen, Y. R. Chi, J. Am. Chem. Soc. 2012, 134, 8810-8813.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 8810-8813
    • Mo, J.1    Chen, X.2    Chi, Y.R.3
  • 39
    • 84855978945 scopus 로고    scopus 로고
    • Phenazine and riboflavin are known to oxidize the alkyl Breslow intermediate to acyl azolium. See:, T. Uno, T. Inokuma, Y. Takemoto, Chem. Commun. 2012, 48, 1901-1903.
    • (2012) Chem. Commun. , vol.48 , pp. 1901-1903
    • Uno, T.1    Inokuma, T.2    Takemoto, Y.3
  • 41
    • 70349942669 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 10119-10122
    • (2008) Angew. Chem. , vol.120 , pp. 10119-10122
  • 42
    • 57549095456 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 9971-9974. For alternative organocatalytic [4+2] reactions, see
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9971-9974
  • 44
    • 70349769741 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5474-5477
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5474-5477
  • 46
    • 84859538802 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 3653-3657.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 3653-3657
  • 51
    • 84861896956 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 5904-5906. For related work, see
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5904-5906


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.