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Volumn 49, Issue 24, 2008, Pages 3858-3861

Synthesis of 6-oxacyclopropa[a]indene derivatives starting from Baylis-Hillman adducts via Pd-mediated C(sp3)-H activation

Author keywords

6 Oxacyclopropa a indene; Activation of C(sp3) H bond; Baylis Hillman adducts; Palladium

Indexed keywords

CARBON; CARBOXYLIC ACID DERIVATIVE; HYDROGEN; INDENE DERIVATIVE; PALLADIUM;

EID: 43049174903     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.04.080     Document Type: Article
Times cited : (66)

References (46)
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    • For our recent papers on Pd-mediated reactions involving modified Baylis-Hillman adducts, see:
    • For our recent papers on Pd-mediated reactions involving modified Baylis-Hillman adducts, see:. Gowrisankar S., Lee H.S., Lee K.Y., Lee J.-E., and Kim J.N. Tetrahedron Lett. 48 (2007) 8619-8622
    • (2007) Tetrahedron Lett. , vol.48 , pp. 8619-8622
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  • 4
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    • For the synthesis and synthetic applications of 6-oxacyclopropa[a]indene-1a-carboxylic acid derivatives, see:
    • For the synthesis and synthetic applications of 6-oxacyclopropa[a]indene-1a-carboxylic acid derivatives, see:. Hedley S.J., Ventura D.L., Dominiak P.M., Nygren C.L., and Davies H.M.L. J. Org. Chem. 71 (2006) 5349-5356
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  • 13
    • 33846246048 scopus 로고    scopus 로고
    • For the synthesis of similar cyclopropane-fused ring compounds, see:
    • For the synthesis of similar cyclopropane-fused ring compounds, see:. Nowak I., Cannon J.F., and Robins M.J. J. Org. Chem. 72 (2007) 532-537
    • (2007) J. Org. Chem. , vol.72 , pp. 532-537
    • Nowak, I.1    Cannon, J.F.2    Robins, M.J.3
  • 22
    • 34248173876 scopus 로고    scopus 로고
    • 3)-H bond activation, see:
    • 3)-H bond activation, see:. Ren H., Li Z., and Knochel P. Chem. Asian J. 2 (2007) 416-433
    • (2007) Chem. Asian J. , vol.2 , pp. 416-433
    • Ren, H.1    Li, Z.2    Knochel, P.3
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    • 2942643950 scopus 로고    scopus 로고
    • For the palladium migration and the following aryl coupling reactions, see:
    • For the palladium migration and the following aryl coupling reactions, see:. Huang Q., Fazio A., Dai G., Campo M.A., and Larock R.C. J. Am. Chem. Soc. 126 (2004) 7460-7461
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 7460-7461
    • Huang, Q.1    Fazio, A.2    Dai, G.3    Campo, M.A.4    Larock, R.C.5
  • 41
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    • The mechanism for the formation of compound 4a could be a β-carbon elimination from intermediate I, followed by decarboxylation. The formation of compound 8 could also be regarded similarly. Further studies on the mechanism are currently underway
    • Sasaki K., Kondo Y., and Maruoka K. Angew. Chem., Int. Ed. 40 (2001) 411-414 The mechanism for the formation of compound 4a could be a β-carbon elimination from intermediate I, followed by decarboxylation. The formation of compound 8 could also be regarded similarly. Further studies on the mechanism are currently underway
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 411-414
    • Sasaki, K.1    Kondo, Y.2    Maruoka, K.3
  • 42
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    • note
    • 4S: C, 68.39; H, 5.50; N, 3.32. Found: C, 68.27; H, 5.38; N, 3.26.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.