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Volumn 22, Issue 14-15, 2011, Pages 1536-1541

Asymmetric synthesis of O-alkylated tetronic acid derivatives via an organocatalytic Mannich reaction and subsequent intramolecular cyclization

Author keywords

[No Author keywords available]

Indexed keywords

CINCHONA ALKALOID; ETHYL 4 CHLORO 3 OXOBUTANOATE; IMINE; OXOACID; PROSTAGLANDIN; PYRROLIDINE DERIVATIVE; TERT BUTYL(2 CHLOROPHENYL)(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(2 METHOXYPHENYL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(4 FLUOROPHENYL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(4 METHOXYPHENYL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(FURAN 2 YL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(FURAN 3 YL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)(THIOPHEN 2 YL)METHYLCARBAMATE; TERT BUTYL(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)[4 (TRIFLUOROMETHYL)PHENYL]METHYLCARBAMATE; TERT BUTYL(3 CHLOROPHENYL)(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)METHYLCARBAMATE; TERT BUTYL(4 CHLOROPHENYL)(2 ETHOXY 4 OXO 4,5 DIHYDROFURAN 3 YL)METHYLCARBAMATE; TERTIARY AMINE; TETRONIC ACID DERIVATIVE; THIOUREA; TRIETHYLAMINE; UNCLASSIFIED DRUG;

EID: 80054878047     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.08.022     Document Type: Article
Times cited : (18)

References (47)
  • 1
    • 1642415515 scopus 로고    scopus 로고
    • For reviews of enantioselective Mannich reactions, see
    • For reviews of enantioselective Mannich reactions, see: A. Córdova Acc. Chem. Res. 37 2004 102
    • (2004) Acc. Chem. Res. , vol.37 , pp. 102
    • Córdova, A.1
  • 5
    • 0037495950 scopus 로고    scopus 로고
    • For metal-based chiral catalysts in asymmetric Mannich reactions of 1,3-dicarbonyl compounds, see
    • For metal-based chiral catalysts in asymmetric Mannich reactions of 1,3-dicarbonyl compounds, see: M. Marigo, A. Kjærsgaard, K. Juhl, N. Gathergood, and K.A. Jørgensen Chem. Eur. J. 9 2003 2359
    • (2003) Chem. Eur. J. , vol.9 , pp. 2359
    • Marigo, M.1    Kjærsgaard, A.2    Juhl, K.3    Gathergood, N.4    Jørgensen, K.A.5
  • 8
    • 48849094479 scopus 로고    scopus 로고
    • For reviews of asymmetric organocatalysis, see
    • For reviews of asymmetric organocatalysis, see: A. Dondoni, and A. Massi Angew. Chem., Int. Ed. 47 2008 4638
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 4638
    • Dondoni, A.1    Massi, A.2
  • 13
    • 23844490047 scopus 로고    scopus 로고
    • For selected examples of organocatalytic Mannich reactions, see
    • For selected examples of organocatalytic Mannich reactions, see: S. Lou, B.M. Taoka, A. Ting, and S.E. Schaus J. Am. Chem. Soc. 127 2005 11256
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 11256
    • Lou, S.1    Taoka, B.M.2    Ting, A.3    Schaus, S.E.4
  • 31
    • 42149107087 scopus 로고    scopus 로고
    • For reviews of tetronic acid derivatives, see
    • For reviews of tetronic acid derivatives, see: R. Schobert, and S. Andrea Bioorg. Med. Chem. 16 2008 4203
    • (2008) Bioorg. Med. Chem. , vol.16 , pp. 4203
    • Schobert, R.1    Andrea, S.2
  • 33
    • 0025318925 scopus 로고
    • For the synthesis of chiral tetronic acid derivatives, see
    • For the synthesis of chiral tetronic acid derivatives, see: T. Donald, D.T. Witiak, and A.K. Tehim J. Org. Chem. 55 1990 1112
    • (1990) J. Org. Chem. , vol.55 , pp. 1112
    • Donald, T.1    Witiak, D.T.2    Tehim, A.K.3
  • 44
    • 80054886316 scopus 로고    scopus 로고
    • 2) was 0.0788 (all data). Absolute structure parameter Flack = -0.005(14).
    • 2) was 0.0788 (all data). Absolute structure parameter Flack = -0.005(14).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.