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Volumn 126, Issue 38, 2004, Pages 11804-11805

Organocatalytic asymmetric aza-Friedel-Crafts alkylation of furan

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; CARBONYL DERIVATIVE; FURAN 2 YLAMINE; FURAN DERIVATIVE; HYDROGEN; NITROGEN DERIVATIVE; PHOSPHORIC ACID; UNCLASSIFIED DRUG;

EID: 4644355914     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja046185h     Document Type: Article
Times cited : (364)

References (71)
  • 1
    • 0026418434 scopus 로고
    • Reviews on atom economy: (a) Trost, B. M. Science 1991, 254, 1471.
    • (1991) Science , vol.254 , pp. 1471
    • Trost, B.M.1
  • 10
  • 15
    • 4644369191 scopus 로고    scopus 로고
    • (h) Special issue on Enantioselective Organocatalysis: Acc. Chem. Res. 2004, 37, no. 8.
    • (2004) Acc. Chem. Res. , vol.37 , Issue.8
  • 16
    • 0345825852 scopus 로고    scopus 로고
    • For selected recent examples of enantioselective organocatalysis via enamine formation, see: (a) Vignola, N.; List, B. J. Am. Chem. Soc. 2004, 126, 450.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 450
    • Vignola, N.1    List, B.2
  • 28
    • 0346865819 scopus 로고    scopus 로고
    • For a review on Brønsted acid catalysis, see: Schreiner, P. R. Chem. Soc. Rev. 2003, 32, 289.
    • (2003) Chem. Soc. Rev. , vol.32 , pp. 289
    • Schreiner, P.R.1
  • 29
    • 0000728050 scopus 로고    scopus 로고
    • For recent examples of chiral Brønsted acid catalysis, see the following. Neutral thiourea derivatives: (a) Su, J. T.; Vachal, P.; Jacobsen. E. N. Adv. Synth. Catal. 2001, 343, 197.
    • (2001) Adv. Synth. Catal. , vol.343 , pp. 197
    • Su, J.T.1    Vachal, P.2    Jacobsen, E.N.3
  • 42
    • 2342521907 scopus 로고    scopus 로고
    • Uraguchi, D.; Terada, M. J. Am. Chem. Soc. 2004, 126, 5356. A similar phosphoric acid has been used for the Mukaiyama-type Mannich reaction; see: Akiyama, T.; Itoh, J.; Yokota, K.; Fuchibe, K. Angew. Chem., Int. Ed. 2004, 43, 1566.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5356
    • Uraguchi, D.1    Terada, M.2
  • 43
    • 2342570203 scopus 로고    scopus 로고
    • Uraguchi, D.; Terada, M. J. Am. Chem. Soc. 2004, 126, 5356. A similar phosphoric acid has been used for the Mukaiyama-type Mannich reaction; see: Akiyama, T.; Itoh, J.; Yokota, K.; Fuchibe, K. Angew. Chem., Int. Ed. 2004, 43, 1566.
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 1566
    • Akiyama, T.1    Itoh, J.2    Yokota, K.3    Fuchibe, K.4
  • 44
    • 0037680718 scopus 로고    scopus 로고
    • Reviews on stereoselective F-C reactions: (a) Jørgensen, K. A. Synthesis 2003, 1117.
    • (2003) Synthesis , pp. 1117
    • Jørgensen, K.A.1
  • 46
    • 0033533951 scopus 로고    scopus 로고
    • For examples of Lewis acid-catalyzed asymmetric 1,2-aza-F-C reactions, see: (a) Johannsen, M. Chem. Commun. 1999, 2233.
    • (1999) Chem. Commun. , pp. 2233
    • Johannsen, M.1
  • 54
    • 0034807741 scopus 로고    scopus 로고
    • For enantioselective organocatalytic 1,4-F-C alkylations of aromatic and heteroaromatic compounds, see: (a) Paras, N. A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2001, 123, 4370.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 4370
    • Paras, N.A.1    MacMillan, D.W.C.2
  • 68
    • 4644267375 scopus 로고    scopus 로고
    • note
    • Investigations of the transition states of the present and previous reactions are underway.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.