메뉴 건너뛰기




Volumn 62, Issue , 2004, Pages 223-227

Enantioenriched axially chiral β-diketimines: Determination of the IAN-amine barrier to atropisomerization

Author keywords

[No Author keywords available]

Indexed keywords

2 NAPHTHYLAMINE; AMINE; BETA DIKETIMINE DERIVATIVE; IMINE; ISOQUINOLINE DERIVATIVE; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0347090298     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (12)

References (16)
  • 1
    • 0003475697 scopus 로고    scopus 로고
    • A. Abiko, Rev. Heteroatom Chem., 1997, 17, 51; H. Waldmann, Organic Synthesis Highlights II, 1995, 49.
    • (1997) Rev. Heteroatom Chem. , vol.17 , pp. 51
    • Abiko, A.1
  • 4
    • 0033714636 scopus 로고    scopus 로고
    • F. Fache, E. Schulz, M. L. Tommasino, and M. Lemaire, Chem. Rev., 2000, 100, 2159; M. Falorni, Trends in Organic Chemistry, 1993, 41, 351.
    • (1993) Trends in Organic Chemistry , vol.41 , pp. 351
    • Falorni, M.1
  • 5
    • 0000236883 scopus 로고
    • H. Fritischi, U. Leutenegger, and A. Pfaltz, Angew. Chem., 1986, 98, 1028; H. Fritischi, U. Leutenegger, and A. Pfaltz, Helv. Chim. Acta, 1988, 71, 1553; U. Leutenegger, A. Madin, and A. Pfaltz, Angew. Chem., 1989, 101, 61. For a similar strategy, see: M. P. Sibi and Y. Asano, J. Am. Chem. Soc., 2001, 123, 9708.
    • (1986) Angew. Chem. , vol.98 , pp. 1028
    • Fritischi, H.1    Leutenegger, U.2    Pfaltz, A.3
  • 6
    • 84986366730 scopus 로고
    • H. Fritischi, U. Leutenegger, and A. Pfaltz, Angew. Chem., 1986, 98, 1028; H. Fritischi, U. Leutenegger, and A. Pfaltz, Helv. Chim. Acta, 1988, 71, 1553; U. Leutenegger, A. Madin, and A. Pfaltz, Angew. Chem., 1989, 101, 61. For a similar strategy, see: M. P. Sibi and Y. Asano, J. Am. Chem. Soc., 2001, 123, 9708.
    • (1988) Helv. Chim. Acta , vol.71 , pp. 1553
    • Fritischi, H.1    Leutenegger, U.2    Pfaltz, A.3
  • 7
    • 0006098805 scopus 로고
    • H. Fritischi, U. Leutenegger, and A. Pfaltz, Angew. Chem., 1986, 98, 1028; H. Fritischi, U. Leutenegger, and A. Pfaltz, Helv. Chim. Acta, 1988, 71, 1553; U. Leutenegger, A. Madin, and A. Pfaltz, Angew. Chem., 1989, 101, 61. For a similar strategy, see: M. P. Sibi and Y. Asano, J. Am. Chem. Soc., 2001, 123, 9708.
    • (1989) Angew. Chem. , vol.101 , pp. 61
    • Leutenegger, U.1    Madin, A.2    Pfaltz, A.3
  • 8
    • 0035802336 scopus 로고    scopus 로고
    • H. Fritischi, U. Leutenegger, and A. Pfaltz, Angew. Chem., 1986, 98, 1028; H. Fritischi, U. Leutenegger, and A. Pfaltz, Helv. Chim. Acta, 1988, 71, 1553; U. Leutenegger, A. Madin, and A. Pfaltz, Angew. Chem., 1989, 101, 61. For a similar strategy, see: M. P. Sibi and Y. Asano, J. Am. Chem. Soc., 2001, 123, 9708.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9708
    • Sibi, M.P.1    Asano, Y.2
  • 11
    • 0034300043 scopus 로고    scopus 로고
    • Biaryl ligands with low barriers to atropisomerization may still be used in asymmetric synthesis: M. Tudor, J. Becker, P. White, and M. Gagne, Organometallics, 2000, 19, 4376.
    • (2000) Organometallics , vol.19 , pp. 4376
    • Tudor, M.1    Becker, J.2    White, P.3    Gagne, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.