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Volumn 136, Issue 39, 2014, Pages 13578-13581

A new iron(III)-salen catalyst for enantioselective Conia-ene carbocyclization

Author keywords

[No Author keywords available]

Indexed keywords

KETONES; SCAFFOLDS;

EID: 84949115941     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja507853f     Document Type: Article
Times cited : (60)

References (29)
  • 24
    • 84862538749 scopus 로고    scopus 로고
    • 3in DCE at 70-80 °C can catalyze Conia-ene cyclization of 4 in the absence of a cocatalyst. See: Chan, L. Y.; Kim, S.; Park, Y.; Lee, P. H. J. Org. Chem. 2012, 77, 5239
    • (2012) J. Org. Chem. , vol.77 , pp. 5239
    • Chan, L.Y.1    Kim, S.2    Park, Y.3    Lee, P.H.4
  • 28
    • 0034637608 scopus 로고    scopus 로고
    • Tricycle 48 can be viewed as a surrogate for the BCD ring system of the mangicols. See: Renner, M. K.; Jensen, P. R.; Fenical, W. J. Org. Chem. 2000, 65, 4843
    • (2000) J. Org. Chem. , vol.65 , pp. 4843
    • Renner, M.K.1    Jensen, P.R.2    Fenical, W.3
  • 29
    • 61449241709 scopus 로고    scopus 로고
    • A similar mechanism has been proposed by Hatakeyama for indium-catalyzed Conia-ene-type carbocyclization (see: Hatakeyama, S. Pure Appl. Chem. 2009, 81, 217). However, alternative mechanisms for metal-catalyzed Conia-ene cyclizations have been considered that do not invoke a metal enolate (see refs 3i, 9, and 10)
    • (2009) Pure Appl. Chem. , vol.81 , pp. 217
    • Hatakeyama, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.