메뉴 건너뛰기




Volumn , Issue 10, 2006, Pages 1557-1571

Air- and moisture-stable secondary phosphine oxides as preligands in catalysis

Author keywords

Asymmetric catalysis; Cross coupling; Nucleophilic additions; Phosphorus; Transition metals

Indexed keywords

AIR; CATALYSIS; CATALYSTS; MOISTURE; PHOSPHORUS COMPOUNDS; TRANSITION METALS;

EID: 33744543074     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926427     Document Type: Review
Times cited : (219)

References (150)
  • 1
    • 0003445429 scopus 로고    scopus 로고
    • Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Berlin
    • Comprehensive Asymmetric Catalysis; Jacobsen, E. N.; Pfaltz, A.; Yamamoto, H., Eds.; Springer: Berlin, 1999.
    • (1999) Comprehensive Asymmetric Catalysis
  • 2
    • 84891580093 scopus 로고    scopus 로고
    • Ojima, I., Ed.; Wiley: New York
    • Catalytic Asymmetric Synthesis; Ojima, I., Ed.; Wiley: New York, 2000.
    • (2000) Catalytic Asymmetric Synthesis
  • 13
    • 4143051292 scopus 로고    scopus 로고
    • For the application of nucleophilic N-heterocyclic carbenes in organocatalysis, see: Enders, D.; Balensiefer, T. Acc. Chem. Res. 2004, 37, 534.
    • (2004) Acc. Chem. Res. , vol.37 , pp. 534
    • Enders, D.1    Balensiefer, T.2
  • 19
    • 9244261559 scopus 로고    scopus 로고
    • For a brief highlight article on the use in enantioselective transition-metal-catalyzed transformations, see: Dubrovina, N. V.; Börner, A. Angew. Chem. Int. Ed. 2004, 43, 5883.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5883
    • Dubrovina, N.V.1    Börner, A.2
  • 21
    • 0000134337 scopus 로고
    • Note that electronegative substituents on phosphorus shift the equilibrium to favor the phosphinous acid: Griffiths, J. E.; Burg, A. B. J. Am. Chem. Soc. 1960, 82, 1507.
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 1507
    • Griffiths, J.E.1    Burg, A.B.2
  • 39
    • 0038547968 scopus 로고    scopus 로고
    • Hydrogen-bond-stabilized quasi chelate ligands were employed in rhodium-catalyzed hydroformylation reactions: (a) Breit, B.; Seiche, W. J. Am. Chem. Soc. 2003, 125, 6608.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6608
    • Breit, B.1    Seiche, W.2
  • 69
    • 14644439830 scopus 로고    scopus 로고
    • and references cited therein
    • (b) Gooßen, L. J.; Dezfuli, M. K. Synlett 2005, 445; and references cited therein.
    • (2005) Synlett , pp. 445
    • Gooßen, L.J.1    Dezfuli, M.K.2
  • 71
    • 33744539031 scopus 로고    scopus 로고
    • (E. I. du Pont de Nemours and Company); US Patent 6124462, 2000
    • Li, G. Y. (E. I. du Pont de Nemours and Company); US Patent 6124462, 2000.
    • Li, G.Y.1
  • 76
    • 0011932271 scopus 로고    scopus 로고
    • Loupy, A., Ed.; Wiley-VCH: Weinheim
    • Microwaves in Organic Synthesis; Loupy, A., Ed.; Wiley-VCH: Weinheim, 2002.
    • (2002) Microwaves in Organic Synthesis
  • 90
  • 93
    • 0033619841 scopus 로고    scopus 로고
    • and references cited therein
    • (b) Mowery, M. E.; DeShong, P. Org. Lett. 1999, 1, 2137; and references cited therein.
    • (1999) Org. Lett. , vol.1 , pp. 2137
    • Mowery, M.E.1    DeShong, P.2
  • 100
    • 0242563114 scopus 로고    scopus 로고
    • Astruc, D., Ed.; Wiley-VCH: Weinheim
    • Hartwig, J. F.; In Modern Arene Chemistry; Astruc, D., Ed.; Wiley-VCH: Weinheim, 2002, 107-168.
    • (2002) Modern Arene Chemistry , pp. 107-168
    • Hartwig, J.F.1
  • 107
    • 33744543033 scopus 로고    scopus 로고
    • Diploma thesis; LMU München: Germany
    • Born, R. Diploma thesis; LMU München: Germany, 2004.
    • (2004)
    • Born, R.1
  • 111
    • 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
  • 123
    • 0001892562 scopus 로고    scopus 로고
    • (a) An example of oxidative addition of a chlorodiaza-phospholene to yield a phosphenium complex: Gudat, D.; Haghverdi, A.; Nieger, M. J. Organomet. Chem. 2001, 617-618, 383.
    • (2001) J. Organomet. Chem. , vol.617-618 , pp. 383
    • Gudat, D.1    Haghverdi, A.2    Nieger, M.3
  • 129
    • 0142227985 scopus 로고    scopus 로고
    • It is interesting to speculate whether such a reactivity is of importance for a triaminophosphine recently employed as ligand for cross-coupling reactions: Urgaonkar, S.; Xu, J.-H.; Verkade, J. G. J. Org. Chem. 2003, 68, 8416.
    • (2003) J. Org. Chem. , vol.68 , pp. 8416
    • Urgaonkar, S.1    Xu, J.-H.2    Verkade, J.G.3
  • 147
    • 0036263823 scopus 로고    scopus 로고
    • For highly enantioselective benzoin homo-coupling reactions using a carbene nucleophile, see: Enders, D.; Kallfass, U. Angew. Chem. Int. Ed. 2002, 41, 1743.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1743
    • Enders, D.1    Kallfass, U.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.