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Volumn 48, Issue 36, 2007, Pages 6252-6257

Organocatalytic asymmetric multi-component [C+NC+CC] synthesis of highly functionalized pyrrolidine derivatives

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOMALONATE DERIVATIVE; ALDEHYDE; ALPHA ALDEHYDE; BETA ALDEHYDE; CARBON; FUNCTIONAL GROUP; MALONIC ACID DERIVATIVE; MOLECULAR SCAFFOLD; NITROGEN; ORGANIC COMPOUND; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34547682312     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.07.031     Document Type: Article
Times cited : (113)

References (82)
  • 14
    • 33947231700 scopus 로고    scopus 로고
    • For reviews on 1,3-dipolar cycloadditions see:
    • For reviews on 1,3-dipolar cycloadditions see:. Pellissier H. Tetrahedron 63 (2007) 3235
    • (2007) Tetrahedron , vol.63 , pp. 3235
    • Pellissier, H.1
  • 74
    • 29944442929 scopus 로고    scopus 로고
    • For other examples of this approach see: and references therein
    • For other examples of this approach see:. Garner P., and Kaniskan H.U. J. Org. Chem. 70 (2005) 10868 and references therein
    • (2005) J. Org. Chem. , vol.70 , pp. 10868
    • Garner, P.1    Kaniskan, H.U.2
  • 75
    • 17144366282 scopus 로고    scopus 로고
    • For an excellent review on the importance of developing asymmetric multi-component reactions see:
    • For an excellent review on the importance of developing asymmetric multi-component reactions see:. Ramon D.J., and Yus M. Angew. Chem., Int. Ed. 44 (2005) 1602
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 1602
    • Ramon, D.J.1    Yus, M.2
  • 76
    • 34547666630 scopus 로고    scopus 로고
    • note
    • After completion of this manuscript an excellent paper by Vicario et al. (Vicario, J. L.; Reboredo, S.; Badia, D.; Carrillo L. Angew. Chem., Int. Ed. 2007, early view) appeared on the web on 30th May describing an organocatalytic reaction between a preformed azomethine ylide derived from diethyl 2-aminomalonate and enals. Notably, catalyst 11 did not catalyze the reaction under their reaction conditions.
  • 79
    • 34547672792 scopus 로고    scopus 로고
    • note
    • R = major enantiomer 15.7 min, minor enantiomer 10.7 min.
  • 80
    • 34547668470 scopus 로고    scopus 로고
    • note
    • 6) requires m/z 412.1755, found 412.1740.
  • 81
    • 34547690773 scopus 로고    scopus 로고
    • note
    • 4) requires m/z 312.1230, found 312.1239.
  • 82
    • 33845279732 scopus 로고    scopus 로고
    • note
    • 4Na) requires m/z 362.1363, found 362.1372. The data matched those for previously reported 16d see: Tsuge, O.; Kanemasa, S.; Yoshioka, M. J. Org. Chem. 1988, 53, 1384.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.