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Volumn 77, Issue 13, 2012, Pages 5613-5623

Role of reversible dimerization in reactions of amphoteric aziridine aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINES; COVALENT INTERACTIONS; DIMER DISSOCIATION; FURTHER DEVELOPMENT; NUCLEOPHILICITIES; REACTIVITY CONTROL;

EID: 84863633019     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3007418     Document Type: Article
Times cited : (20)

References (62)
  • 34
    • 0002054640 scopus 로고    scopus 로고
    • Aziridines and azirines: Monocyclic
    • In; Katritzky, A. R. Rees, C. W. Scriven, E. F. V. Elsevier: Oxford, Vol.
    • Pearson, W. H.; Lian, B. W.; Bergmeier, S. C. Aziridines and Azirines: Monocyclic. In Comprehensive Heterocyclic Chemistry II; Katritzky, A. R.; Rees, C. W.; Scriven, E. F. V., Eds.; Elsevier: Oxford, 1996; Vol. 1A, p 8.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.1 , pp. 8
    • Pearson, W.H.1    Lian, B.W.2    Bergmeier, S.C.3
  • 37
  • 40
    • 15044358964 scopus 로고    scopus 로고
    • A very interesting case reported by the Somfai group documents α-tosylamino aldehyde with very similar connectivity.
    • A very interesting case reported by the Somfai group documents α-tosylamino aldehyde with very similar connectivity. Restorp, P.; Somfai, P. Org. Lett. 2005, 7, 893-895
    • (2005) Org. Lett. , vol.7 , pp. 893-895
    • Restorp, P.1    Somfai, P.2
  • 51
    • 77955586031 scopus 로고    scopus 로고
    • Chemoselectivepeptidomimetic ligation is the main application of the resulting diamine building blocks
    • Chemoselectivepeptidomimetic ligation is the main application of the resulting diamine building blocks: Assem, N.; Natarajan, A.; Yudin, A. K. J. Am. Chem. Soc. 2010, 132, 10986-10987
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10986-10987
    • Assem, N.1    Natarajan, A.2    Yudin, A.K.3
  • 53
    • 33845191735 scopus 로고    scopus 로고
    • a units in comparison to their corresponding amines. This ensures that the aniline Schiff base is significantly protonated compared to the oxime. The transamination of the more populated protonated aniline imine to the oxime is significantly faster than imine formation with a weakly protonated carbonyl group.
    • a units in comparison to their corresponding amines. This ensures that the aniline Schiff base is significantly protonated compared to the oxime. The transamination of the more populated protonated aniline imine to the oxime is significantly faster than imine formation with a weakly protonated carbonyl group.
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 7581-7584
    • Dirksen, A.1    Hackeng, T.M.2    Dawson, P.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.