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Volumn 505, Issue 7483, 2014, Pages 386-390

Erratum: Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling (Nature (2014) 505 (386-390) DOI: 10.1038/nature12781);Asymmetric synthesis from terminal alkenes by cascades of diboration and cross-coupling

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALCOHOL; ALKENE DERIVATIVE; AMINE; FUNCTIONAL GROUP; OXIDIZING AGENT; REDUCING AGENT;

EID: 84892589818     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature13040     Document Type: Erratum
Times cited : (190)

References (30)
  • 1
    • 0033740673 scopus 로고    scopus 로고
    • Selectivity in propene polymerization with metallocene catalysts
    • Resconi, L., Cavallo, L., Fait, A. & Piemontesi, F. Selectivity in propene polymerization with metallocene catalysts. Chem. Rev. 100, 1253-1345 (2000)
    • (2000) Chem. Rev , vol.100 , pp. 1253-1345
    • Resconi, L.1    Cavallo, L.2    Fait, A.3    Piemontesi, F.4
  • 2
    • 67650422263 scopus 로고    scopus 로고
    • Highly asymmetric cobalt-catalyzed aziridination of alkenes with trichloroethoxysulfonyl azide (TcesN3)
    • Subbarayan, V., Ruppel, J. V., Zhu, S., Perman, J. A. & Zhang, X. P. Highly asymmetric cobalt-catalyzed aziridination of alkenes with trichloroethoxysulfonyl azide (TcesN3). Chem. Commun. 4266-4268 (2009)
    • (2009) Chem. Commun , pp. 4266-4268
    • Subbarayan, V.1    Ruppel, J.V.2    Zhu, S.3    Perman, J.A.4    Zhang, X.P.5
  • 3
    • 85007835900 scopus 로고
    • Catalytic asymmetric synthesis of optically active 2-alkanols via hydrosilylation of 1-alkenes with a chiral monophosphinepalladium catalyst
    • Uozumi, Y. & Hayashi, T. Catalytic asymmetric synthesis of optically active 2-alkanols via hydrosilylation of 1-alkenes with a chiral monophosphinepalladium catalyst. J. Am. Chem. Soc. 113, 9887-9888 (1991)
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 9887-9888
    • Uozumi, Y.1    Hayashi, T.2
  • 4
    • 0032494390 scopus 로고    scopus 로고
    • A new class of planar2chiral ligands: Synthesis of a C2-symmetric bisazaferrocene and its application in the enantioselective Cu(I)-catalyzed cyclopropanation of olefins
    • Lo, M. M.-C. & Fu, G. C. A new class of planar2chiral ligands: synthesis of a C2-symmetric bisazaferrocene and its application in the enantioselective Cu(I)-catalyzed cyclopropanation of olefins. J.Am. Chem. Soc. 120, 10270-10271 (1998)
    • (1998) J.Am. Chem. Soc , vol.120 , pp. 10270-10271
    • Lo, M.M.-C.1    Fu, G.C.2
  • 5
    • 33750247077 scopus 로고    scopus 로고
    • A newligand class for the asymmetric dihydroxylation of olefins
    • Becker, H.&Sharpless, K. B.A newligand class for the asymmetric dihydroxylation of olefins. Angew. Chem. Int. Edn Engl. 35, 448-451 (1996)
    • (1996) Angew Chem. Int. Edn Engl , vol.35 , pp. 448-451
    • Becker, H.1    Sharpless, K.B.2
  • 6
    • 84857938093 scopus 로고    scopus 로고
    • An asymmetric hydroformylation catalyst that delivers branched aldehydes from alkyl alkenes
    • Noonan, G. M., Fuentes, J. A., Cobley, C. J. & Clarke, M. L. An asymmetric hydroformylation catalyst that delivers branched aldehydes from alkyl alkenes. Angew. Chem. Int. Edn Engl. 51, 2477-2480 (2012)
    • (2012) Angew. Chem. Int. Edn Engl , vol.51 , pp. 2477-2480
    • Noonan, G.M.1    Fuentes, J.A.2    Cobley, C.J.3    Clarke, M.L.4
  • 7
    • 84881052216 scopus 로고    scopus 로고
    • Scope andmechanismof the Pt-catalyzed enantioselective diboration ofmonosubstituted alkenes
    • Coombs, J. R.,Haefner, F., Kliman, L. T.&Morken, J. P. Scope andmechanismof the Pt-catalyzed enantioselective diboration ofmonosubstituted alkenes. J.Am. Chem. Soc. 135, 11222-11231 (2013)
    • (2013) J.Am. Chem. Soc , vol.135 , pp. 11222-11231
    • Coombs, R.1    Haefner, J.F.2    Kliman, L.T.3    Morken, J.P.4
  • 8
    • 0742304172 scopus 로고    scopus 로고
    • Catalytic asymmetric carbohydroxylation of alkenes by a tandem diboration/Suzuki cross-coupling/ oxidation reaction
    • Miller, S. P., Morgan, J. B., Nepveux, F. J. & Morken, J. P. Catalytic asymmetric carbohydroxylation of alkenes by a tandem diboration/Suzuki cross-coupling/ oxidation reaction. Org. Lett. 6, 131-133 (2004)
    • (2004) Org. Lett , vol.6 , pp. 131-133
    • Miller, S.P.1    Morgan, J.B.2    Nepveux, F.J.3    Morken, J.P.4
  • 9
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura, N. & Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 95, 2457-2483 (1995)
    • (1995) Chem. Rev , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 10
    • 79952656192 scopus 로고    scopus 로고
    • Advances in transition metal (Pd, Ni, Fe)-catalyzed cross coupling reactions using alkyl-organometallics as reaction partners
    • Jana, R., Pathak, T. P. & Sigman, M. S. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross coupling reactions using alkyl-organometallics as reaction partners. Chem. Rev. 111, 1417-1492 (2011)
    • (2011) Chem. Rev , vol.111 , pp. 1417-1492
    • Jana, R.1    Pathak, T.P.2    Sigman, M.S.3
  • 11
    • 73249139284 scopus 로고    scopus 로고
    • Vicinal diboronates in high enantiomeric purity through tandem site-selective NHC-Cu-catalyzed boron-copper additions to terminal alkynes
    • Lee, Y., Jang, H. & Hoveyda, A. H. Vicinal diboronates in high enantiomeric purity through tandem site-selective NHC-Cu-catalyzed boron-copper additions to terminal alkynes. J. Am. Chem. Soc. 131, 18234-18235 (2009)
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 18234-18235
    • Lee, Y.1    Jang, H.2    Hoveyda, A.H.3
  • 12
    • 79951832916 scopus 로고    scopus 로고
    • Distinguishing between pathways for transmetallation in Suzuki-Miyaura reactions
    • Carrow, B. P.&Hartwig, J. F. Distinguishing between pathways for transmetallation in Suzuki-Miyaura reactions. J. Am. Chem. Soc. 133, 2116-2119 (2011)
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 2116-2119
    • Carrow, B.P.1    Hartwig, J.F.2
  • 13
    • 79951662418 scopus 로고    scopus 로고
    • Kinetic data for the transmetalation/reductive elimination in palladium-catalyzed Suzuki-Miyaura reactions: Unexpected triple role of hydroxide ions used as base
    • Amatore, C., Jutand, A. & Le Duc, G. Kinetic data for the transmetalation/reductive elimination in palladium-catalyzed Suzuki-Miyaura reactions: unexpected triple role of hydroxide ions used as base. Chemistry 17, 2492-2503 (2011)
    • (2011) Chemistry , vol.17 , pp. 2492-2503
    • Amatore, C.1    Jutand, A.2    Le Duc, G.3
  • 14
    • 0000971633 scopus 로고    scopus 로고
    • Alkylboranes in the Suzuki-Miyaura coupling: Stereochemical and mechanistic studies
    • Matos, K. & Soderquist, J. A. Alkylboranes in the Suzuki-Miyaura coupling: stereochemical and mechanistic studies. J. Org. Chem. 63, 461-470 (1998)
    • (1998) J. Org. Chem , vol.63 , pp. 461-470
    • Matos, K.1    Soderquist, J.A.2
  • 15
    • 0002965803 scopus 로고
    • Cross-coupling reaction of alkyl- or arylboronic acid esters with organic halides induced by thallium(I) salts and palladium catalyst
    • Sato, M., Miyaura, N. & Suzuki, A. Cross-coupling reaction of alkyl- or arylboronic acid esters with organic halides induced by thallium(I) salts and palladium catalyst. Chem. Lett. 18, 1405-1408 (1989)
    • (1989) Chem. Lett , vol.18 , pp. 1405-1408
    • Sato, M.1    Miyaura, N.2    Suzuki, A.3
  • 16
    • 0035920614 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross coupling of lithium n-alkylborates
    • Zou, G. & Falck, J. R. Suzuki-Miyaura cross coupling of lithium n-alkylborates. Tetrahedr. Lett. 42, 5817-5819 (2001)
    • (2001) Tetrahedr. Lett , vol.42 , pp. 5817-5819
    • Zou, G.1    Falck, J.R.2
  • 17
    • 12344337689 scopus 로고    scopus 로고
    • Monoligated palladium species as catalysts in cross-coupling reactions
    • Christmann, U. & Vilar, R. Monoligated palladium species as catalysts in cross-coupling reactions. Angew. Chem. Int. Edn Engl. 44, 366-374 (2005)
    • (2005) Angew. Chem. Int. Edn Engl , vol.44 , pp. 366-374
    • Christmann, U.1    Vilar, R.2
  • 18
    • 84855464257 scopus 로고    scopus 로고
    • Alkylboronic esters from copper-catalyzed borylation of primary and secondary alkyl halides and pseudohalides
    • Yang, C.-T. et al. Alkylboronic esters from copper-catalyzed borylation of primary and secondary alkyl halides and pseudohalides. Angew. Chem. Int. Edn Engl. 51, 528-532 (2012)
    • (2012) Angew. Chem. Int. Edn Engl , vol.51 , pp. 528-532
    • Yang, C.-T.1
  • 19
    • 24944477864 scopus 로고    scopus 로고
    • Efficient Pd-catalyzed amination of heteroaryl halides
    • Charles, M. D., Schultz, P. & Buchwald, S. L. Efficient Pd-catalyzed amination of heteroaryl halides. Org. Lett. 7, 3965-3968 (2005)
    • (2005) Org. Lett , vol.7 , pp. 3965-3968
    • Charles, M.D.1    Schultz, P.2    Buchwald, S.L.3
  • 21
    • 77955574719 scopus 로고    scopus 로고
    • Chemoselective and regiospecific Suzuki coupling on a multisubstituted sp3 carbon in 1,1-diborylalkanes at room temperature
    • Endo, K., Ohkubo, T., Hirokami, M. & Shibata, T. Chemoselective and regiospecific Suzuki coupling on a multisubstituted sp3 carbon in 1,1-diborylalkanes at room temperature. J. Am. Chem. Soc. 132, 11033-11035 (2010)
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 11033-11035
    • Endo, K.1    Ohkubo, T.2    Hirokami, M.3    Shibata, T.4
  • 22
    • 0000311321 scopus 로고    scopus 로고
    • Transmetalation of alkylboranes to palladiumin the Suzuki coupling reaction proceeds with retention of stereochemistry
    • Ridgway, B. H.&Woerpel, K. A. Transmetalation of alkylboranes to palladiumin the Suzuki coupling reaction proceeds with retention of stereochemistry. J. Org. Chem. 63, 458-460 (1998)
    • (1998) J. Org. Chem , vol.63 , pp. 458-460
    • Ridgway, B.H.1    Woerpel, K.A.2
  • 23
    • 83755178261 scopus 로고    scopus 로고
    • Catalytic enantioselective allylation of carbonyl compounds and imines
    • Yus, M., González-Gómez, J. C. & Foubelo, F. Catalytic enantioselective allylation of carbonyl compounds and imines. Chem. Rev. 111, 7774-7854 (2011)
    • (2011) Chem. Rev , vol.111 , pp. 7774-7854
    • Yus, M.1    González-Gómez, J.C.2    Foubelo, F.3
  • 24
    • 84873635491 scopus 로고    scopus 로고
    • Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols
    • Silverio, D. L. et al. Simple organic molecules as catalysts for enantioselective synthesis of amines and alcohols. Nature 494, 216-221 (2013)
    • (2013) Nature , vol.494 , pp. 216-221
    • Silverio, D.L.1
  • 26
    • 84867338504 scopus 로고    scopus 로고
    • Direct stereospecific amination of alkyl and aryl pinacol boronates
    • Mlynarski, S. N., Karns, A. S. & Morken, J. P. Direct stereospecific amination of alkyl and aryl pinacol boronates. J. Am. Chem. Soc. 134, 16449-16451 (2012)
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 16449-16451
    • Mlynarski, S.N.1    Karns, A.S.2    Morken, J.P.3
  • 27
    • 0001175929 scopus 로고
    • Lithium: Efficient generation and capture by boronic esters and a simple preparation of diisopropyl (chloromethyl)boronate
    • Sadhu, K. M. & Matteson, D. S. (Chloromethyl)lithium: efficient generation and capture by boronic esters and a simple preparation of diisopropyl (chloromethyl)boronate. Organometallics 4, 1687-1689 (1985)
    • (1985) Organometallics , vol.4 , pp. 1687-1689
    • Sadhu, K.M.1    Matteson, D.S.2
  • 28
    • 84985520733 scopus 로고
    • 3-Phenylpropylamines: A new class of systemic fungicides
    • Himmele, W. & Pommer, E.-H. 3-Phenylpropylamines: a new class of systemic fungicides. Angew. Chem. Int. Edn Engl. 19, 184-189 (1980)
    • (1980) Angew. Chem. Int. Edn Engl , vol.19 , pp. 184-189
    • Himmele, W.1    Pommer, E.-H.2
  • 29
    • 0027527574 scopus 로고
    • An efficient enantioselective total synthesis of antitumor lignans: Synthesis of enantiomerically pure 4-hydroxyalkanenitriles via an enzymatic reaction
    • Itoh, T., Chika, J., Takagi, Y. & Nishiyama, S. An efficient enantioselective total synthesis of antitumor lignans: synthesis of enantiomerically pure 4-hydroxyalkanenitriles via an enzymatic reaction. J. Org. Chem. 58, 5717-5723 (1993)
    • (1993) J. Org. Chem , vol.58 , pp. 5717-5723
    • Itoh, T.1    Chika, J.2    Takagi, Y.3    Nishiyama, S.4


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