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Volumn 53, Issue 41, 2014, Pages 11041-11045

Kinetic resolution of 1,1-biaryl-2,2-diols and amino alcohols through NHC-catalyzed atroposelective acylation

Author keywords

acylation; axial chirality; enantioselectivity; kinetic resolution; N heterocyclic carbene

Indexed keywords

AMINO ALCOHOLS; CATALYSIS; ENANTIOSELECTIVITY; KINETICS; ORGANIC COMPOUNDS;

EID: 84911138320     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201406192     Document Type: Article
Times cited : (184)

References (82)
  • 6
    • 33746270803 scopus 로고    scopus 로고
    • For selected recent examples, see
    • Angew. Chem. 2005, 117, 5518-5563; For selected recent examples, see
    • (2005) Angew. Chem. , vol.117 , pp. 5518-5563
  • 8
    • 53349134274 scopus 로고    scopus 로고
    • Angew. Chem. 2007, 119, 4025-4028
    • (2007) Angew. Chem. , vol.119 , pp. 4025-4028
  • 12
    • 79960219653 scopus 로고    scopus 로고
    • Angew. Chem. 2011, 123, 5231-5235
    • (2011) Angew. Chem. , vol.123 , pp. 5231-5235
  • 17
    • 84896755712 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 9463-9465
    • (2013) Angew. Chem. , vol.125 , pp. 9463-9465
  • 21
    • 84918811167 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 3758-3761
    • (2014) Angew. Chem. , vol.126 , pp. 3758-3761
  • 23
    • 84925366257 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 5562-5565.
    • (2014) Angew. Chem. , vol.126 , pp. 5562-5565
  • 25
    • 41849139741 scopus 로고    scopus 로고
    • PRPR 45
    • J. M. Brunel, Chem. Rev. 2007, 107, PR 1 -PR 45
    • (2007) Chem. Rev. , vol.107 , pp. 1
    • Brunel, J.M.1
  • 26
    • 84882418057 scopus 로고    scopus 로고
    • (Ed.: Q.-L. Zhou), Wiley, Hoboken For selected review and reports on NOBIN, see
    • M. Shibasaki, S. Matsunaga, in Privileged Chiral Ligands and Catalysts (Ed.:, Q.-L. Zhou,), Wiley, Hoboken, 2011, pp. 295-332; For selected review and reports on NOBIN, see
    • (2011) Privileged Chiral Ligands and Catalysts , pp. 295-332
    • Shibasaki, M.1    Matsunaga, S.2
  • 30
    • 84882392356 scopus 로고    scopus 로고
    • BINAP (2,2-Bis(diphenylphosphino)-1,1-binaphthyl), a privileged chiral ligand in asymmetric catalysis, is prepared from BINOL. For a recent review, see:, in (Ed.: Q.-L. Zhou), Wiley, Hoboken
    • BINAP (2,2-Bis(diphenylphosphino)-1,1-binaphthyl), a privileged chiral ligand in asymmetric catalysis, is prepared from BINOL. For a recent review, see:, T. Ohkuma, N. Kurono, in Privileged Chiral Ligands and Catalysts (Ed.:, Q.-L. Zhou,), Wiley, Hoboken, 2011, pp. 1-53.
    • (2011) Privileged Chiral Ligands and Catalysts , pp. 1-53
    • Ohkuma, T.1    Kurono, N.2
  • 31
    • 85026893086 scopus 로고    scopus 로고
    • For other selected examples using HPLC separation or an interesting mechanochemical approach, see
    • D. Cai, D. L. Hughes, T. R. Verhoeven, P. J. Reider, Org. Synth. 1999, 76, 1-3; For other selected examples using HPLC separation or an interesting mechanochemical approach, see
    • (1999) Org. Synth. , vol.76 , pp. 1-3
    • Cai, D.1    Hughes, D.L.2    Verhoeven, T.R.3    Reider, P.J.4
  • 34
    • 84862195619 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 1672-1675.
    • (2012) Angew. Chem. , vol.124 , pp. 1672-1675
  • 35
    • 77956683709 scopus 로고    scopus 로고
    • For selected examples, see
    • H. Wang, Chirality 2010, 22, 827-837; For selected examples, see
    • (2010) Chirality , vol.22 , pp. 827-837
    • Wang, H.1
  • 43
    • 0000261561 scopus 로고
    • For catalytic asymmetric methods, see
    • R. J. Kazlauskas, J. Am. Chem. Soc. 1989, 111, 4953-4959; For catalytic asymmetric methods, see
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4953-4959
    • Kazlauskas, R.J.1
  • 46
    • 84925365532 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 14450-14453.
    • (2013) Angew. Chem. , vol.125 , pp. 14450-14453
  • 55
    • 38049013578 scopus 로고    scopus 로고
    • Angew. Chem. 2007, 119, 8623-8626
    • (2007) Angew. Chem. , vol.119 , pp. 8623-8626
  • 63
    • 84874270779 scopus 로고    scopus 로고
    • Angew. Chem. 2012, 124, 11854-11866
    • (2012) Angew. Chem. , vol.124 , pp. 11854-11866
  • 70
    • 84882375092 scopus 로고    scopus 로고
    • Angew. Chem. 2013, 125, 1775-1778
    • (2013) Angew. Chem. , vol.125 , pp. 1775-1778
  • 74
    • 17444417515 scopus 로고    scopus 로고
    • For kinetic resolution of cyclic secondary amines using an achiral NHC catalyst and a chiral hydroxamic acids, see
    • T. Kano, K. Sasaki, K. Maruoka, Org. Lett. 2005, 7, 1347-1349; For kinetic resolution of cyclic secondary amines using an achiral NHC catalyst and a chiral hydroxamic acids, see
    • (2005) Org. Lett. , vol.7 , pp. 1347-1349
    • Kano, T.1    Sasaki, K.2    Maruoka, K.3
  • 82
    • 84882395487 scopus 로고    scopus 로고
    • For a recent review, see:, in (Ed.: Q.-L. Zhou), Wiley, Hoboken
    • For a recent review, see:, S.-F. Zhu, Q.-L. Zhou, in Privileged Chiral Ligands and Catalysts (Ed.:, Q.-L. Zhou,), Wiley, Hoboken, 2011, pp. 137-170.
    • (2011) Privileged Chiral Ligands and Catalysts , pp. 137-170
    • Zhu, S.-F.1    Zhou, Q.-L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.