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Volumn 4, Issue 2, 2007, Pages 115-124

An update on catalytic enantioselective alkylations of indoles

Author keywords

Alkylation; Asymmetric catalysis; Friedel crafts; Indoles

Indexed keywords

ACTIVATION ANALYSIS; ADDITION REACTIONS; BIOACTIVITY; ORGANOMETALLICS;

EID: 34248664085     PISSN: 1570193X     EISSN: None     Source Type: Journal    
DOI: 10.2174/157019307780599270     Document Type: Article
Times cited : (23)

References (61)
  • 4
    • 85189268396 scopus 로고    scopus 로고
    • Sundberg, R.J, Ed, Academic Press, London
    • (a) Sundberg, R.J., Ed.; Indoles, Academic Press, London, 1996.
    • (1996) Indoles
  • 6
    • 85189266812 scopus 로고    scopus 로고
    • For examples of simple monodentate enones as electrophiles for enantioselective indole alkylations see: (a) Bandini, M, Fagioli, F, Melchiorre, P, Melloni, A, Umani-Ronchi, A. Tetrahedron Lett, 2003, 44, 5843
    • For examples of simple monodentate enones as electrophiles for enantioselective indole alkylations see: (a) Bandini, M.; Fagioli, F.; Melchiorre, P.; Melloni, A.; Umani-Ronchi, A. Tetrahedron Lett., 2003, 44, 5843.
  • 8
    • 85017640581 scopus 로고    scopus 로고
    • For seminal studies concerning the enantioselective organocatalyzed 1,4-conjugate addition of electron-ring aromatics to enals see: a
    • For seminal studies concerning the enantioselective organocatalyzed 1,4-conjugate addition of electron-ring aromatics to enals see: (a) Paras, N.A.; MacMillan, D.W.C. J. Am. Chem. Soc., 2001, 123, 4370.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 4370
    • Paras, N.A.1    MacMillan, D.W.C.2
  • 22
    • 0036625219 scopus 로고    scopus 로고
    • For a recent review on bifunctional catalysts in asymmetric transformations see
    • For a recent review on bifunctional catalysts in asymmetric transformations see: Shibasaki, M.; Yoshikawa, N. Chem. Rev., 2002, 102, 2187.
    • (2002) Chem. Rev , vol.102 , pp. 2187
    • Shibasaki, M.1    Yoshikawa, N.2
  • 26
    • 85189279986 scopus 로고    scopus 로고
    • Only one example of FC nitroalkenes bearing an alkyl group at the β-position was reported (Y: 57%, ee: 70%).
    • Only one example of FC nitroalkenes bearing an alkyl group at the β-position was reported (Y: 57%, ee: 70%).
  • 35
    • 1442360753 scopus 로고    scopus 로고
    • Grubbs, R.H, Ed, Wiley-VCH, Weinheim
    • (a) Handbook of Metathesis, Grubbs, R.H., Ed.; Wiley-VCH, Weinheim, 2003.
    • (2003) Handbook of Metathesis
  • 38
    • 25144440011 scopus 로고    scopus 로고
    • For some representative examples see: a
    • For some representative examples see: (a) Zeng, X.-F.; Ji, S.-J.; Wang, S.-Y. Tetrahedron, 2005, 61, 10235.
    • (2005) Tetrahedron , vol.61 , pp. 10235
    • Zeng, X.-F.1    Ji, S.-J.2    Wang, S.-Y.3
  • 60
    • 33744510833 scopus 로고    scopus 로고
    • Dyker, G, Ed, Wiley-VCH, Weinheim
    • Handbook of C-H Transformations, Dyker, G., Ed.; Wiley-VCH, Weinheim, 2005.
    • (2005) Handbook of C-H Transformations


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.