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Volumn 129, Issue 17, 2007, Pages 5334-5335

Highly stereoselective formal [3 + 3] cycloaddition of enals and azomethine imines catalyzed by N-heterocyclic carbenes

Author keywords

[No Author keywords available]

Indexed keywords

CARBENOID; IMINE;

EID: 34247874549     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0709167     Document Type: Article
Times cited : (291)

References (45)
  • 1
    • 11544346529 scopus 로고    scopus 로고
    • For reviews of intermolecular cycloadditions, see: a
    • For reviews of intermolecular cycloadditions, see: (a) Gothelf, K. V.; Jorgensen, K. A. Chem. Rev. 1998, 98, 863-909.
    • (1998) Chem. Rev , vol.98 , pp. 863-909
    • Gothelf, K.V.1    Jorgensen, K.A.2
  • 14
  • 16
    • 33645410218 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: Schantl, J. G. Sci. Synth. 2004, 27, 731-824.
    • (2004) Sci. Synth , vol.27 , pp. 731-824
    • Schantl, J.G.1
  • 28
    • 85022816667 scopus 로고
    • For early homoenolate studies, see: a
    • For early homoenolate studies, see: (a) Nickhorn, A.; Lambert, J. L. J. Am. Chem. Soc. 1964, 86, 4604-4605.
    • (1964) J. Am. Chem. Soc , vol.86 , pp. 4604-4605
    • Nickhorn, A.1    Lambert, J.L.2
  • 37
    • 0038441546 scopus 로고    scopus 로고
    • For recent formal [3 + 3] cycloadditions, see: (a) Hedley, S. J.; Moran, W. J.; Price, D. A.; Harrity, J. P. A. J. Org. Chem. 2003, 68, 4286-4292.
    • For recent formal [3 + 3] cycloadditions, see: (a) Hedley, S. J.; Moran, W. J.; Price, D. A.; Harrity, J. P. A. J. Org. Chem. 2003, 68, 4286-4292.
  • 43
    • 34247898389 scopus 로고    scopus 로고
    • Azomethine imines lacking the phenyl substituent on the ring afford products, but in reduced yields
    • Azomethine imines lacking the phenyl substituent on the ring afford products, but in reduced yields.
  • 44
    • 34247858148 scopus 로고    scopus 로고
    • The Z(O) enol isomer of I in IV minimizes interactions between the N-mesityl group and the imine phenyl ring.
    • The Z(O) enol isomer of I in IV minimizes interactions between the N-mesityl group and the imine phenyl ring.
  • 45
    • 34247872011 scopus 로고
    • Additional studies on the synthetic utility of these unusual heterocycles are ongoing
    • Laurent, E.; Lee, S. K.; Pellissier, N. J. Chem. Res. Miniprint 1978, 5201-5218. Additional studies on the synthetic utility of these unusual heterocycles are ongoing.
    • (1978) J. Chem. Res. Miniprint , pp. 5201-5218
    • Laurent, E.1    Lee, S.K.2    Pellissier, N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.