메뉴 건너뛰기




Volumn 436, Issue 7054, 2005, Pages 1139-1140

Catalytic enantioselective reactions driven by photoinduced electron transfer

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; HYDROGEN BONDS; LIGHT ABSORPTION; MOLECULAR STRUCTURE; SOLAR ENERGY; STOICHIOMETRY;

EID: 24144502430     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/nature03955     Document Type: Article
Times cited : (409)

References (15)
  • 1
    • 10044254637 scopus 로고    scopus 로고
    • The complex architecture of oxygenic photosynthesis
    • Nelson, N. & Ben-Shem, A. The complex architecture of oxygenic photosynthesis. Nature Rev. Mol. Cell Biol. 5, 971-982 (2004).
    • (2004) Nature Rev. Mol. Cell Biol. , vol.5 , pp. 971-982
    • Nelson, N.1    Ben-Shem, A.2
  • 4
    • 0037055113 scopus 로고    scopus 로고
    • Highly enantioselective intra- And intermolecular [2+2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: Host-guest interactions, product configuration, and the origin of the stereoselectivity in solution
    • Bach, T., Bergmann, H., Grosch, B. & Harms, K. Highly enantioselective intra- and intermolecular [2+2] photocycloaddition reactions of 2-quinolones mediated by a chiral lactam host: Host-guest interactions, product configuration, and the origin of the stereoselectivity in solution. J. Am. Chem. Soc. 124, 7982-7990 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 7982-7990
    • Bach, T.1    Bergmann, H.2    Grosch, B.3    Harms, K.4
  • 6
    • 85020071329 scopus 로고    scopus 로고
    • (eds Inoue, Y. & Ramamurthy, V.) (M. Dekker, New York)
    • Inoue, Y. in Molecular and Supramoiecuiar Photochemistry Vol. 11 (eds Inoue, Y. & Ramamurthy, V.) 129-177 (M. Dekker, New York, 2004).
    • (2004) Molecular and Supramoiecuiar Photochemistry , vol.11 , pp. 129-177
    • Inoue, Y.1
  • 7
    • 0033601065 scopus 로고    scopus 로고
    • Trapped optically active (E)-cycloheptene generated by enantiodifferentiating Z-E photoisomerization of cycloheptene sensitized by chiral aromatic esters
    • Hoffmann, R. & Inoue, Y. Trapped optically active (E)-cycloheptene generated by enantiodifferentiating Z-E photoisomerization of cycloheptene sensitized by chiral aromatic esters. J. Am. Chem. Soc. 121, 10702-10710 (1999).
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 10702-10710
    • Hoffmann, R.1    Inoue, Y.2
  • 8
    • 0037433567 scopus 로고    scopus 로고
    • Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1- alkenes photosensitized by saccharide naphthalenecarboxylates
    • Asaoka, S., Wada, T. & Inoue, Y. Microenvironmental polarity control of electron-transfer photochirogenesis. Enantiodifferentiating polar addition of 1,1-diphenyl-1-alkenes photosensitized by saccharide naphthalenecarboxylates. J. Am. Chem. Soc. 125, 3008-3027 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 3008-3027
    • Asaoka, S.1    Wada, T.2    Inoue, Y.3
  • 9
    • 0000435361 scopus 로고
    • Radical cyclization reactions of α-silyl amine α,β- unsaturated ketone and ester systems promoted by single electron transfer photosensitization
    • Jeon, Y. T., Lee, C.-P. & Mariano, P. S. Radical cyclization reactions of α-silyl amine α,β-unsaturated ketone and ester systems promoted by single electron transfer photosensitization. J. Am. Chem. Soc. 113, 8847-8863 (1991).
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 8847-8863
    • Jeon, Y.T.1    Lee, C.-P.2    Mariano, P.S.3
  • 10
    • 0033934707 scopus 로고    scopus 로고
    • Highly efficient and stereoselective radical addition of tertiary amines to electron-deficient alkenes - Application to the enantioselective synthesis of necine bases
    • Bertrand, S., Hoffmann, N. & Pete, J.-P. Highly efficient and stereoselective radical addition of tertiary amines to electron-deficient alkenes-Application to the enantioselective synthesis of necine bases. Eur. J. Org. Chem., 2227-2238 (2000).
    • (2000) Eur. J. Org. Chem. , pp. 2227-2238
    • Bertrand, S.1    Hoffmann, N.2    Pete, J.-P.3
  • 11
    • 0037013591 scopus 로고    scopus 로고
    • Enantioselective Norrish-Yang cyclization reactions of N-(ω-oxoalkyl)substituted imidazolidinones in solution and in the solid state
    • Bach, T., Aechtner, T. & Neumüller, B. Enantioselective Norrish-Yang cyclization reactions of N-(ω-oxoalkyl)substituted imidazolidinones in solution and in the solid state. Chem. Eur. J. 8, 2464-2475 (2002).
    • (2002) Chem. Eur. J. , vol.8 , pp. 2464-2475
    • Bach, T.1    Aechtner, T.2    Neumüller, B.3
  • 12
    • 8844275954 scopus 로고    scopus 로고
    • Hydrogen bond mediated enantioselectivity of radical reactions
    • Aechtner, T., Dressel, T. & Bach, T. Hydrogen bond mediated enantioselectivity of radical reactions. Angew. Chem. Int. Edn Engl. 43, 5849-5851 (2004).
    • (2004) Angew. Chem. Int. Edn Engl. , vol.43 , pp. 5849-5851
    • Aechtner, T.1    Dressel, T.2    Bach, T.3
  • 13
    • 0036034678 scopus 로고    scopus 로고
    • Optical rotation: Recent advances in determining the absolute configuration
    • Polavarapu, P. L. Optical rotation: Recent advances in determining the absolute configuration. Chirality 14, 768-781 (2002).
    • (2002) Chirality , vol.14 , pp. 768-781
    • Polavarapu, P.L.1
  • 14
    • 0037431283 scopus 로고    scopus 로고
    • Systematic investigation of modern quantum chemical methods to predict electronic circular dichroism spectra
    • Diedrich, C. & Grimme, S. Systematic investigation of modern quantum chemical methods to predict electronic circular dichroism spectra. J. Phys. Chem. A 107, 2524-2539 (2003).
    • (2003) J. Phys. Chem. A , vol.107 , pp. 2524-2539
    • Diedrich, C.1    Grimme, S.2
  • 15
    • 0842328916 scopus 로고    scopus 로고
    • 1H-NMR shift reagent for the ee determination of chiral lactams, quinolones, and oxazolidinones
    • 1H-NMR shift reagent for the ee determination of chiral lactams, quinolones, and oxazolidinones. J. Org. Chem. 69, 970-973 (2004).
    • (2004) J. Org. Chem. , vol.69 , pp. 970-973
    • Bergmann, H.1    Grosch, B.2    Sitterberg, S.3    Bach, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.