메뉴 건너뛰기




Volumn 49, Issue 29-30, 2008, Pages 4537-4541

Binaphthyl substituted 1,8-bis(dimethylamino)naphthalenes, the first chiral, atropisomeric, proton sponges

Author keywords

1,1 Binaphthyl; 1,8 Bis(dimethylamino)naphthalene; Atropisomers; Chiral proton sponge

Indexed keywords

NAPHTHALENE DERIVATIVE;

EID: 44749085371     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.05.042     Document Type: Article
Times cited : (15)

References (59)
  • 2
    • 44749087719 scopus 로고    scopus 로고
    • For reviews, see:. Rappoport Z. (Ed), J. Wiley & Sons, Chichester Chapter 17
    • For reviews, see:. Pozharskii A.F., and Ozeryanskii V.A. In: Rappoport Z. (Ed). The Chemistry of Anilines (2007), J. Wiley & Sons, Chichester 931-1026 Chapter 17
    • (2007) The Chemistry of Anilines , pp. 931-1026
    • Pozharskii, A.F.1    Ozeryanskii, V.A.2
  • 7
    • 0000958574 scopus 로고
    • Angew. Chem. 100 (1988) 895-909
    • (1988) Angew. Chem. , vol.100 , pp. 895-909
  • 17
    • 2042493111 scopus 로고
    • Angew. Chem. 98 (1986) 460-462
    • (1986) Angew. Chem. , vol.98 , pp. 460-462
  • 19
    • 2042419216 scopus 로고
    • Angew. Chem. 95 (1983) 748-749
    • (1983) Angew. Chem. , vol.95 , pp. 748-749
  • 32
    • 30544447821 scopus 로고    scopus 로고
    • Brønsted acid salts of bis(amidine) ligands derived from (+)-trans-cyclohexane diamine have been used as efficient chiral proton catalysts in enantioselective aza-Henry reactions, but despite features similar to proton sponge, they do not possess an identifiable increase in Brønsted basicity relative to their component functionality:
    • Brønsted acid salts of bis(amidine) ligands derived from (+)-trans-cyclohexane diamine have been used as efficient chiral proton catalysts in enantioselective aza-Henry reactions, but despite features similar to proton sponge, they do not possess an identifiable increase in Brønsted basicity relative to their component functionality:. Hess A.S., Yoder R.A., and Johnston J.N. Synlett (2006) 147-149
    • (2006) Synlett , pp. 147-149
    • Hess, A.S.1    Yoder, R.A.2    Johnston, J.N.3
  • 46
    • 44749088537 scopus 로고    scopus 로고
    • note
    • +/MS and C, H, N analysis). Their synthesis and full characterisation are reported in the Supplementary data.
  • 55
    • 0000718373 scopus 로고    scopus 로고
    • Pu L. Chem. Rev. 98 (1998) 2405-2494
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 58
    • 42949087964 scopus 로고    scopus 로고
    • Dutot, L.; Wright, K.; Gaucher, A.; Wakselman, M.; Mazaleyrat, J.-P.; Peggion, C.; Formaggio, F.; Toniolo, C. J. Am. Chem. Soc. 2008, 130, in press (doi: doi:10.1021/ja800059d).
    • Dutot, L.; Wright, K.; Gaucher, A.; Wakselman, M.; Mazaleyrat, J.-P.; Peggion, C.; Formaggio, F.; Toniolo, C. J. Am. Chem. Soc. 2008, 130, in press (doi: doi:10.1021/ja800059d).
  • 59
    • 43049130704 scopus 로고    scopus 로고
    • Dutot, L.; Wright, K.; Wakselman, M.; Mazaleyrat, J.-P.; Peggion, C.; De Zotti, M.; Formaggio, F.; Toniolo, C. Tetrahedron Lett. 2008, in press (doi: doi:10.1016/j.tetlet.2008.03.087).
    • Dutot, L.; Wright, K.; Wakselman, M.; Mazaleyrat, J.-P.; Peggion, C.; De Zotti, M.; Formaggio, F.; Toniolo, C. Tetrahedron Lett. 2008, in press (doi: doi:10.1016/j.tetlet.2008.03.087).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.