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Volumn 16, Issue 48, 2010, Pages 14232-14240

Asymmetric hydrogenation of minimally functionalised terminal olefins: An alternative sustainable and direct strategy for preparing enantioenriched hydrocarbons

Author keywords

carbene ligands; hydrogenation; iridium; olefins; P ligands

Indexed keywords

ASYMMETRIC HYDROGENATION; CARBENE LIGANDS; CATALYST DESIGNS; CATALYTIC PRECURSORS; CATALYTIC SYSTEM; IMINOPHOSPHORANES; LANTHANIDES; LATEST DEVELOPMENT; P LIGANDS; TERMINAL OLEFINS;

EID: 78651234242     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001909     Document Type: Review
Times cited : (92)

References (70)
  • 1
    • 78651254162 scopus 로고    scopus 로고
    • For metal-mediated decarbonylation of aldehydes, see
    • For metal-mediated decarbonylation of aldehydes, see
  • 3
    • 37349031135 scopus 로고    scopus 로고
    • for a deracemisation by using chiral auxiliaries, see
    • Angew. Chem. Int. Ed. 2007, 46, 9331-9334; for a deracemisation by using chiral auxiliaries, see
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 9331-9334
  • 7
    • 20644452249 scopus 로고    scopus 로고
    • for a cross-coupling reaction of chiral alkylsilanes with aryl triflates, see
    • Angew. Chem. Int. Ed. 2005, 44, 3588-3591; for a cross-coupling reaction of chiral alkylsilanes with aryl triflates, see
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3588-3591
  • 8
    • 54149115435 scopus 로고
    • for an asymmetric carbometallation of terminal olefins, see
    • Y. Hatanaka, T. Hiyama, J. Am. Chem. Soc. 1990, 112, 7793-7794; for an asymmetric carbometallation of terminal olefins, see
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 7793-7794
    • Hatanaka, Y.1    Hiyama, T.2
  • 9
    • 0000375175 scopus 로고    scopus 로고
    • for asymmetric hydroboration of terminal olefins, see
    • P. Wipf, S. Ribe, Org. Lett. 2000, 2, 1713-1716; for asymmetric hydroboration of terminal olefins, see
    • (2000) Org. Lett. , vol.2 , pp. 1713-1716
    • Wipf, P.1    Ribe, S.2
  • 14
    • 0003445429 scopus 로고    scopus 로고
    • (Eds.: E.N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Heidelberg
    • J. M. Brown, in Comprehensive Asymmetric Catalysis, Vol.1 (Eds.:, E.N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, Heidelberg, 1999.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1
    • Brown, J.M.1
  • 15
    • 78651237377 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see
  • 21
  • 26
    • 33747233073 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 5194-5197
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 5194-5197
  • 41
    • 78651240038 scopus 로고    scopus 로고
    • Unpublished results (i.e., for 2-phenylbut-1-ene, ees up to 41%)
    • Unpublished results (i.e., for 2-phenylbut-1-ene, ees up to 41%).
  • 46
    • 67649649888 scopus 로고    scopus 로고
    • Recently, a Ir/phosphine-pinene catalyst precursor has provided enantioselectivities up to 90% in the reduction of few vinylphosphinates, see
    • Recently, a Ir/phosphine-pinene catalyst precursor has provided enantioselectivities up to 90% in the reduction of few vinylphosphinates, see:, X. Meng, X. Li, D. Xu, Tetrahedron: Asymmetry 2009, 20, 1402-1406.
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 1402-1406
    • Meng, X.1    Li, X.2    Xu, D.3
  • 49
    • 78651233441 scopus 로고    scopus 로고
    • See, for instance
    • See, for instance
  • 51
  • 56
    • 78651248506 scopus 로고    scopus 로고
    • For some representative examples, see
    • For some representative examples, see
  • 61
  • 68
    • 34547737512 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 5971-5974.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5971-5974


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.