메뉴 건너뛰기




Volumn 23, Issue 22-23, 2012, Pages 1596-1606

Binap-silver salts as chiral catalysts for the enantioselective 1,3-dipolar cycloaddition of azomethine ylides and alkenes

Author keywords

[No Author keywords available]

Indexed keywords

1,2 BIS(PHENYLSULFONYL)ETHYLENE; ALKENE; AZOMETHINE YLIDE DERIVATIVE; CRISPINE; HARMICINE; MALEIMIDE DERIVATIVE; SILVER DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84870286784     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2012.10.015     Document Type: Article
Times cited : (30)

References (38)
  • 2
    • 0026003250 scopus 로고
    • For the pioneering catalytic enantioselective 1,3-DC work carried out by Grigg et al., see P. Allway, and R. Grigg Tetrahedron Lett. 32 1991 5817 5820.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 5817-5820
    • Allway, P.1    Grigg, R.2
  • 4
    • 33947231700 scopus 로고    scopus 로고
    • The enantioselective 1,3-DC of azomethine ylides is a prolific area in organic synthesis and is frequently reviewed. For selected recent examples, see: H. Pellissier Tetrahedron 63 2007 3235 3285.
    • (2007) Tetrahedron , vol.63 , pp. 3235-3285
    • Pellissier, H.1
  • 15
    • 33646453057 scopus 로고    scopus 로고
    • 4 catalyzed the reaction with phenyl vinyl sulfone (up to 26% ee)
    • 4 catalyzed the reaction with phenyl vinyl sulfone (up to 26% ee). T. Llamas, R. Gómez-Arrayás, and J.C. Carretero Org. Lett. 8 2006 1795 1798.
    • (2006) Org. Lett. , vol.8 , pp. 1795-1798
    • Llamas, T.1    Gómez-Arrayás, R.2    Carretero, J.C.3
  • 16
    • 0347916937 scopus 로고    scopus 로고
    • 2 catalyzed the reaction with maleimides (up to 64-65% ee of the corresponding exo-adduct)
    • 2 catalyzed the reaction with maleimides (up to 64-65% ee of the corresponding exo-adduct). Y. Oderaotoshi, W. Cheng, S. Fujitomi, Y. Kasano, S. Minakata, and M. Komatsu Org. Lett. 5 2003 5043 5046.
    • (2003) Org. Lett. , vol.5 , pp. 5043-5046
    • Oderaotoshi, Y.1    Cheng, W.2    Fujitomi, S.3    Kasano, Y.4    Minakata, S.5    Komatsu, M.6
  • 17
    • 77956697078 scopus 로고    scopus 로고
    • 2 catalyzed the reaction with maleimides, maleates, acrylates, vinylic sulfones, etc. (up to 99% ee)., and corringendum, 2010, 21, 2559
    • 2 catalyzed the reaction with maleimides, maleates, acrylates, vinylic sulfones, etc. (up to 99% ee). M. Martín-Rodríguez, C. Nájera, J.M. Sansano, and F.L. Wu Tetrahedron: Asymmetry 21 2010 1184 1186 and corringendum, 2010, 21, 2559.
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 1184-1186
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3    Wu, F.L.4
  • 19
    • 79960781694 scopus 로고    scopus 로고
    • 2 has been studied and compared with several silver complexes in the elaboration of the key precursor of the 2nd generation GSK-inhibitors of the virus responsible for hepatitis C
    • 2 has been studied and compared with several silver complexes in the elaboration of the key precursor of the 2nd generation GSK-inhibitors of the virus responsible for hepatitis C: M. Martín-Rodríguez, C. Nájera, J.M. Sansano, A. de Cózar, and F.P. Cossío Beilstein J. Org. Chem. 7 2011 988 996.
    • (2011) Beilstein J. Org. Chem. , vol.7 , pp. 988-996
    • Martín-Rodríguez, M.1    Nájera, C.2    Sansano, J.M.3    De Cózar, A.4    Cossío, F.P.5
  • 20
    • 35548957834 scopus 로고    scopus 로고
    • For enantioselective gold(I)-catalyzed cycloadditions dealing with azlactones see: A.D. Melhado, M. Luparia, and F.D. Toste J. Am. Chem. Soc. 129 2007 12638 12639.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12638-12639
    • Melhado, A.D.1    Luparia, M.2    Toste, F.D.3
  • 23
    • 84871234587 scopus 로고    scopus 로고
    • Unpublished estimated data calculated by F. P. Cossío and A. de Cózar (University of the Basque Country)
    • Unpublished estimated data calculated by F. P. Cossío and A. de Cózar (University of the Basque Country).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.