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Volumn 52, Issue 8, 2011, Pages 872-874

Chemoselective 1,3-dipolar cycloadditions of azomethine ylide with conjugated dienes

Author keywords

[No Author keywords available]

Indexed keywords

3 CARBOXY 4 VINYL PYRROLIDINE; ALKENE; AZOMETHINE YLIDE; CARBOXYLIC ACID; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 78751580236     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.12.042     Document Type: Article
Times cited : (13)

References (65)
  • 10
    • 0038576749 scopus 로고    scopus 로고
    • W.H. Pearson, and P. Stoy Synlett 7 2003 903 921 For examples of 1,3 dipolar cycloadditions of nonstabilized azomethine ylides:
    • (2003) Synlett , vol.7 , pp. 903-921
    • Pearson, W.H.1    Stoy, P.2
  • 37
  • 48
    • 78751582595 scopus 로고    scopus 로고
    • version 7.6, Schrödinger, LLC, New York, NY, 2009. A full summary of these calculations is found in the Supplementary Data for this publication
    • Calculations of the HOMO LUMO energies and orbital coefficients have been done with Jaguar, version 7.6, Schrödinger, LLC, New York, NY, 2009. A full summary of these calculations is found in the Supplementary Data for this publication.
    • Calculations of the HOMO LUMO Energies and Orbital Coefficients Have Been Done with Jaguar
  • 59
    • 78751577814 scopus 로고    scopus 로고
    • 1,3-Cycloadditions to nitro olefins and cyan olefins are known
    • 1,3-Cycloadditions to nitro olefins and cyan olefins are known.
  • 65
    • 78751585717 scopus 로고    scopus 로고
    • 1H NMR of the crude mix, (1a/13a 6.7:1) we were unable to definitively determine the relative amount of bis adduct 14a
    • 1H NMR of the crude mix, (1a/13a 6.7:1) we were unable to definitively determine the relative amount of bis adduct 14a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.