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Volumn 75, Issue 6, 2010, Pages 2039-2043

N-Heterocyclic carbene-ruthenium complexes for the racemization of chiral Alcohols

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL EQUATIONS; CHIRAL ALCOHOLS; N-HETEROCYCLIC CARBENE LIGANDS; N-HETEROCYCLIC CARBENES; RUTHENIUM COMPLEXES;

EID: 77949808439     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1001005     Document Type: Article
Times cited : (36)

References (59)
  • 11
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    • For a review on enzymatic racemization: (g)
    • For a review on enzymatic racemization: (g) Schnell, B.; Faber, K.; Kroutil, W. Adv. Synth, Catal. 2003, 345, 653-666.
    • (2003) Adv. Synth, Catal. , vol.345 , pp. 653-666
    • Schnell, B.1    Faber, K.2    Kroutil, W.3
  • 12
    • 39649107133 scopus 로고    scopus 로고
    • For a review on racemization catalysts in DKR: (a)
    • For a review on racemization catalysts in DKR: (a) Ahn, Y.; Ko, S.-B.; Kim, M.-J.; Park, J. Coord. Chem Rev. 2008, 252, 647-658.
    • (2008) J. Coord. Chem Rev. , vol.252 , pp. 647-658
    • Ahn, Y.1    Ko, S.-B.2    Kim, M.-J.3
  • 15
    • 33846184753 scopus 로고    scopus 로고
    • Other organometallic species can facilitate racemization processes. For examples of Ir-based systems, see: (a)
    • Other organometallic species can facilitate racemization processes. For examples of Ir-based systems, see: (a) Stirling, M.; Blacker, A. J.; Page, M. I. Tetrahedron Lett. 2007,48, 1247-1250.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 1247-1250
    • Stirling, M.1    Blacker, A.J.2    Page, M.I.3
  • 27
    • 77949803510 scopus 로고    scopus 로고
    • One example of a 16-electron ruthenium complex, a derivative of the Noyori catalyst, has been patented for the DKR reaction: Verzijl, G. K.; De Vries, J. G.; Broxterman, Q. B. WO/2001/090396, 2001.
    • (a) One example of a 16-electron ruthenium complex, a derivative of the Noyori catalyst, has been patented for the DKR reaction: Verzijl, G. K.; De Vries, J. G.; Broxterman, Q. B. WO/2001/090396, 2001.
  • 28
    • 0042335717 scopus 로고    scopus 로고
    • The activity of a putative 16-electron ruthenium species has been reported in alcohol racemization
    • (b) The activity of a putative 16-electron ruthenium species has been reported in alcohol racemization: Ito, M.; Osaku, A.; Kitahara, S.; Hirakawa, M.; Ikariya, T. Tetrahedron Lett 2003, 44, 7521-7523.
    • (2003) Tetrahedron Lett , vol.44 , pp. 7521-7523
    • Ito, M.1    Osaku, A.2    Kitahara, S.3    Hirakawa, M.4    Ikariya, T.5
  • 29
    • 77949824218 scopus 로고    scopus 로고
    • For rare examples of NHC in racemization reaction with Rh and Ir, see refs 3d and 5c.
    • For rare examples of NHC in racemization reaction with Rh and Ir, see refs 3d and 5c.
  • 30
    • 84908659806 scopus 로고    scopus 로고
    • For uses of NHC ligands in late-transition-metal catalysis, see
    • For uses of NHC ligands in late-transition-metal catalysis, see: Díez-González, S.; Marion, N.; Nolan, S. P. Chem. Rev. 2009, 109, 3612-3676.
    • (2009) Chem. Rev. , vol.109 , pp. 3612-3676
    • Díz-González, S.1    Marion, N.2    Nolan, S.P.3
  • 54
    • 77949802502 scopus 로고    scopus 로고
    • For a review on bifunctional catalysts, see: (b)
    • For a review on bifunctional catalysts, see: (b) Bcariya, T.; Blacker, A. J. Acc. Chem. Res. 2007, 40, 1300-1308.
    • (2007) J. Acc. Chem. Res. , vol.40 , pp. 1300-1308
    • Bcariya, T.1    Blacker, A.2
  • 58
    • 9644257463 scopus 로고    scopus 로고
    • For reviews on ruthenium hydride complexes, see: (a)
    • For reviews on ruthenium hydride complexes, see: (a) Clapham, S. E.; Hadzovic, A.; Morris, R. H. Coord. Chem, Rev. 2004, 248, 2201-2237.
    • (2004) Coord. Chem, Rev. , vol.248 , pp. 2201-2237
    • Clapham, S.E.1    Hadzovic, A.2    Morris, R.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.