메뉴 건너뛰기




Volumn 6, Issue , 2015, Pages

Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; CARBENE; HEXANE;

EID: 84949526866     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms10041     Document Type: Article
Times cited : (25)

References (66)
  • 3
    • 33745742273 scopus 로고    scopus 로고
    • Chiral auxiliaries - Principles and recent applications
    • Gnas, Y. & Glorius, F. Chiral auxiliaries - principles and recent applications. Synthesis 12, 1899-1930 (2006
    • (2006) Synthesis , vol.12 , pp. 1899-1930
    • Gnas, Y.1    Glorius, F.2
  • 4
    • 0030810476 scopus 로고    scopus 로고
    • Pseudoephedrine as a practical chiral auxiliary for the synthesis of highly enantiomerically enriched carboxylic acids, alcohols, aldehydes, and ketones
    • Myers, A. G. et al. Pseudoephedrine as a practical chiral auxiliary for the synthesis of highly enantiomerically enriched carboxylic acids, alcohols, aldehydes, and ketones. J. Am. Chem. Soc. 119, 6496-6511 (1997
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 6496-6511
    • Myers, A.G.1
  • 5
    • 11844283363 scopus 로고    scopus 로고
    • Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)Cl: Access to enantiomerically enriched allcarbon quaternary centers
    • Doyle, A. G. & Jacobsen, E. N. Enantioselective alkylations of tributyltin enolates catalyzed by Cr(salen)Cl: access to enantiomerically enriched allcarbon quaternary centers. J. Am. Chem. Soc. 127, 62-63 (2005
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 62-63
    • Doyle, A.G.1    Jacobsen, E.N.2
  • 6
    • 79957865972 scopus 로고    scopus 로고
    • A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts synthesis of catalyst libraries and evaluation of catalyst activity
    • Denmark, S. E., Gould, N. D. & Wolf, L. M. A systematic investigation of quaternary ammonium ions as asymmetric phase-transfer catalysts. synthesis of catalyst libraries and evaluation of catalyst activity. J. Org. Chem. 76, 4260-4336 (2011
    • (2011) J. Org. Chem , vol.76 , pp. 4260-4336
    • Denmark, S.E.1    Gould, N.D.2    Wolf, L.M.3
  • 7
    • 38349148300 scopus 로고    scopus 로고
    • Recent development and application of chiral phase-transfer catalysts
    • Hashimoto, T. & Maruoka, K. Recent development and application of chiral phase-transfer catalysts. Chem. Rev. 107, 5656-5682 (2007
    • (2007) Chem. Rev , vol.107 , pp. 5656-5682
    • Hashimoto, T.1    Maruoka, K.2
  • 8
    • 0345825852 scopus 로고    scopus 로고
    • Catalytic asymmetric intramolecular a-Alkylation of aldehydes
    • Vignola, N. & List, B. Catalytic asymmetric intramolecular a-Alkylation of aldehydes. J. Am. Chem. Soc. 126, 450-451 (2004
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 450-451
    • Vignola, N.1    List, B.2
  • 9
    • 84890926781 scopus 로고    scopus 로고
    • The catalytic asymmetric a-benzylation of aldehydes
    • List, B. et al. The catalytic asymmetric a-benzylation of aldehydes. Angew. Chem. Int. Ed. Engl 53, 282-285 (2014
    • (2014) Angew. Chem. Int. Ed. Engl , vol.53 , pp. 282-285
    • List, B.1
  • 10
    • 77955816969 scopus 로고    scopus 로고
    • Enantioselective catalytic a-Alkylation of aldehydes via an SN1 pathway
    • Brown, A. R., Kuo, W.-H. & Jacobsen, E. N. Enantioselective catalytic a-Alkylation of aldehydes via an SN1 pathway. J. Am. Chem. Soc. 132, 9286-9288 (2010
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 9286-9288
    • Brown, A.R.1    Kuo, W.-H.2    Jacobsen, E.N.3
  • 11
    • 55249108726 scopus 로고    scopus 로고
    • Prolinecatalyzed asymmetric formal a-Alkylation of aldehydes via vinylogous iminium ion intermediates generated from arylsulfonyl indoles
    • Shaikh, R. R., Mazzanti, A., Petrini, M., Bartoli, G. & Melchiorre, P. Prolinecatalyzed asymmetric formal a-Alkylation of aldehydes via vinylogous iminium ion intermediates generated from arylsulfonyl indoles. Angew. Chem. Int. Ed. Engl. 47, 8707-8710 (2010
    • (2010) Angew. Chem. Int. Ed. Engl , vol.47 , pp. 8707-8710
    • Shaikh, R.R.1    Mazzanti, A.2    Petrini, M.3    Bartoli, G.4    Melchiorre, P.5
  • 13
    • 54749100733 scopus 로고    scopus 로고
    • Organocatalytic asymmetric domino reactions: A cascade consisting of a michael addition and an aldehyde a-Alkylation
    • Enders, D., Wang, C. & Bats, J. W. Organocatalytic asymmetric domino reactions: a cascade consisting of a michael addition and an aldehyde a-Alkylation. Angew. Chem. Int. Ed. Engl. 47, 7539-7542 (2008
    • (2008) Angew. Chem. Int. Ed. Engl , vol.47 , pp. 7539-7542
    • Enders, D.1    Wang, C.2    Bats, J.W.3
  • 14
    • 80051747006 scopus 로고    scopus 로고
    • Highly enantioselective a Alkylation of aldehydes with 1, 3-benzodithiolylium tetrafluoroborate: A formal organocatalytic a Alkylation of aldehydes by the carbenium ion
    • Gualandi, A., Emer, E., Capdevila, M. G. & Cozzi, P. G. Highly enantioselective a Alkylation of aldehydes with 1, 3-benzodithiolylium tetrafluoroborate: a formal organocatalytic a Alkylation of aldehydes by the carbenium ion. Angew. Chem. Int. Ed. Engl. 50, 7842-7846 (2011
    • (2011) Angew. Chem. Int. Ed. Engl , vol.50 , pp. 7842-7846
    • Gualandi, A.1    Emer, E.2    Capdevila, M.G.3    Cozzi, P.G.4
  • 15
    • 84855535325 scopus 로고    scopus 로고
    • Enantio- and diastereoselective organocatalytic a-Alkylation of aldehydes with 3-substituted 2-(bromomethyl)acrylates
    • Jiménez, J. et al. Enantio- and diastereoselective organocatalytic a-Alkylation of aldehydes with 3-substituted 2-(bromomethyl)acrylates. J. Org. Chem. 77, 747-753 (2012
    • (2012) J. Org. Chem , vol.77 , pp. 747-753
    • Jiménez, J.1
  • 16
    • 53849138773 scopus 로고    scopus 로고
    • One-pot organocatalytic domino michael/a-Alkylation reactions: Direct catalytic enantioselective cyclopropanation and cyclopentanation reactions
    • Ibrahem, I. et al. One-pot organocatalytic domino michael/a-Alkylation reactions: direct catalytic enantioselective cyclopropanation and cyclopentanation reactions. Chem. Eur. J 14, 7867-7879 (2008
    • (2008) Chem. Eur. J. , vol.14 , pp. 7867-7879
    • Ibrahem, I.1
  • 17
    • 33646573235 scopus 로고    scopus 로고
    • Direct catalytic intermolecular a-Allylic alkylation of aldehydes by combination of transition-metal and organocatalysis
    • Ibrahem, I. & Córdova, A. Direct catalytic intermolecular a-Allylic alkylation of aldehydes by combination of transition-metal and organocatalysis. Angew. Chem. Int. Ed. Engl. 45, 1952-1956 (2006
    • (2006) Angew. Chem. Int. Ed. Engl , vol.45 , pp. 1952-1956
    • Ibrahem, I.1    Córdova, A.2
  • 18
    • 84873978454 scopus 로고    scopus 로고
    • C-Alkylation of chiral tropane- and homotropane-derived enamines
    • Hodgson, D. M., Charlton, A., Paton, R. S. & Thompson, A. L. C-Alkylation of chiral tropane- and homotropane-derived enamines. J. Org. Chem. 78, 1508-1518 (2013
    • (2013) J. Org. Chem , vol.78 , pp. 1508-1518
    • Hodgson, D.M.1    Charlton, A.2    Paton, R.S.3    Thompson, A.L.4
  • 19
    • 84930225184 scopus 로고    scopus 로고
    • Enantioselective organocatalytic alkylation of aldehydes and enals driven by the direct photoexcitation of enamines
    • Silvi, M., Arceo, E., Jurberg, I. D., Cassani, C. & Melchiorre, P. Enantioselective organocatalytic alkylation of aldehydes and enals driven by the direct photoexcitation of enamines. J. Am. Chem. Soc. 137, 6120-6123 (2015
    • (2015) J. Am. Chem. Soc , vol.137 , pp. 6120-6123
    • Silvi, M.1    Arceo, E.2    Jurberg, I.D.3    Cassani, C.4    Melchiorre, P.5
  • 20
    • 84904788203 scopus 로고    scopus 로고
    • The direct anti-Markovnikov addition of mineral acids to styrenes
    • Wilger, D. J., Grandjean, J. M., Lammert, T. & Nicewicz, D. A. The direct anti-Markovnikov addition of mineral acids to styrenes. Nat. Chem 6, 720-726 (2014
    • (2014) Nat. Chem , vol.6 , pp. 720-726
    • Wilger, D.J.1    Grandjean, J.M.2    Lammert, T.3    Nicewicz, D.A.4
  • 22
    • 0001781293 scopus 로고    scopus 로고
    • Cyclopropane derivatives and their diverse biological activities
    • Salaün, J. Cyclopropane derivatives and their diverse biological activities. Top. Curr. Chem. 207, 1-67 (2000
    • (2000) Top. Curr. Chem , vol.207 , pp. 1-67
    • Salaün, J.1
  • 23
    • 70350512114 scopus 로고    scopus 로고
    • Heterocycles from cyclopropanes: Applications in natural product synthesis
    • Carson, C. A. & Kerr, M. A. Heterocycles from cyclopropanes: applications in natural product synthesis. Chem. Soc. Rev. 38, 3051-3060 (2009
    • (2009) Chem. Soc. Rev , vol.38 , pp. 3051-3060
    • Carson, C.A.1    Kerr, M.A.2
  • 24
    • 70350515235 scopus 로고    scopus 로고
    • Application of donor/acceptor-carbenoids to the synthesis of natural products
    • Davies, H. M. L. & Denton, J. R. Application of donor/acceptor-carbenoids to the synthesis of natural products. Chem. Soc. Rev. 38, 3061-3071 (2009
    • (2009) Chem. Soc. Rev , vol.38 , pp. 3061-3071
    • Davies, H.M.L.1    Denton, J.R.2
  • 25
    • 84870981240 scopus 로고    scopus 로고
    • Recent applications of cyclopropane-based strategies to natural product synthesis
    • Tang, P. & Qin, Y. Recent applications of cyclopropane-based strategies to natural product synthesis. Synthesis 44, 2969-2984 (2012
    • (2012) Synthesis , vol.44 , pp. 2969-2984
    • Tang, P.1    Qin, Y.2
  • 27
    • 33748765777 scopus 로고    scopus 로고
    • Enantioselective catalytic intramolecular cyclopropanation using modified cinchona alkaloid organocatalysts
    • Johansson, C. C. C. et al. Enantioselective catalytic intramolecular cyclopropanation using modified cinchona alkaloid organocatalysts. Angew. Chem. Int. Ed. Engl. 45, 6024-6028 (2006
    • (2006) Angew. Chem. Int. Ed. Engl , vol.45 , pp. 6024-6028
    • Johansson, C.C.C.1
  • 28
    • 77249149393 scopus 로고    scopus 로고
    • Intramolecular Simmons-Smith cyclopropanation studies into the reactivity of alkyl-substituted zinc carbenoids, effect of directing groups and synthesis of bicyclo[n.1.0]alkanes
    • Bull, J. A. & Charette, A. B. Intramolecular Simmons-Smith cyclopropanation. studies into the reactivity of alkyl-substituted zinc carbenoids, effect of directing groups and synthesis of bicyclo[n.1.0]alkanes. J. Am. Chem. Soc. 132, 1895-1902 (2010
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 1895-1902
    • Bull, J.A.1    Charette, A.B.2
  • 29
    • 84915746246 scopus 로고    scopus 로고
    • Enantioselective iron-catalyzed intramolecular cyclopropanation reactions
    • Shen, J.-J. et al. Enantioselective iron-catalyzed intramolecular cyclopropanation reactions. Angew. Chem. Int. Ed. Engl. 53, 13188-13191 (2014
    • (2014) Angew. Chem. Int. Ed. Engl , vol.53 , pp. 13188-13191
    • Shen, J.-J.1
  • 30
    • 3242691284 scopus 로고    scopus 로고
    • Platinum-and gold-catalyzed cycloisomerization reactions of hydroxylated enynes
    • Mamane, V., Gress, T., Krause, H. & Fürstner, A. Platinum- and gold-catalyzed cycloisomerization reactions of hydroxylated enynes. J. Am. Chem. Soc. 126, 8654-8655 (2004
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 8654-8655
    • Mamane, V.1    Gress, T.2    Krause, H.3    Fürstner, A.4
  • 31
    • 3242713858 scopus 로고    scopus 로고
    • PtCl2-catalyzed cycloisomerizations of 5-en-1-yn-3-ol systems
    • Harrak, Y. et al. PtCl2-catalyzed cycloisomerizations of 5-en-1-yn-3-ol systems. J. Am. Chem. Soc. 126, 8656-8657 (2004
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 8656-8657
    • Harrak, Y.1
  • 32
    • 4444291533 scopus 로고    scopus 로고
    • Catalaytic isomerization of 1, 5-enynes to bicyclo[3.1.0]hexenes
    • Luzung, M. R., Markham, J. P. & Toste, F. D. Catalaytic isomerization of 1, 5-enynes to bicyclo[3.1.0]hexenes. J. Am. Chem. Soc. 126, 10858-10859 (2004
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 10858-10859
    • Luzung, M.R.1    Markham, J.P.2    Toste, F.D.3
  • 33
    • 33749505253 scopus 로고    scopus 로고
    • Gold(I) catalyzed isomerization of 5-en-2-yn-1-yl acetates: An efficient access to acetoxy bicyclo[3.1.0]hexenes and 2-cycloalken-1-ones
    • Buzas, A. & Gagosz, F. Gold(I) catalyzed isomerization of 5-en-2-yn-1-yl acetates: an efficient access to acetoxy bicyclo[3.1.0]hexenes and 2-cycloalken-1-ones. J. Am. Chem. Soc. 128, 12614-12615 (2006
    • (2006) J. Am. Chem. Soc , vol.128 , pp. 12614-12615
    • Buzas, A.1    Gagosz, F.2
  • 34
    • 80052306516 scopus 로고    scopus 로고
    • Copper-mediated aerobic synthesis of 3-Azabicyclo[3.1.0]hex-2-enes and 4-Carbonylpyrroles from N-Allyl/propargyl enamine carboxylates
    • Toh, K. K., Wang, Y.-F., Ng, E. P. J. & Chiba, S. Copper-mediated aerobic synthesis of 3-Azabicyclo[3.1.0]hex-2-enes and 4-Carbonylpyrroles from N-Allyl/propargyl enamine carboxylates. J. Am. Chem. Soc. 133, 13942-13945 (2011
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 13942-13945
    • Toh, K.K.1    Wang, Y.-F.2    Ng, E.P.J.3    Chiba, S.4
  • 35
    • 34247542965 scopus 로고    scopus 로고
    • A palladium-catalyzed cyclization-oxidation sequence: Synthesis of Bicyclo[3.1.0]hexanes and evidence for SN2 C-O bond formation
    • Tong, X., Beller, M. & Tse, M. K. A palladium-catalyzed cyclization-oxidation sequence: synthesis of Bicyclo[3.1.0]hexanes and evidence for SN2 C-O bond formation. J. Am. Chem. Soc. 129, 4906-4907 (2007
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 4906-4907
    • Tong, X.1    Beller, M.2    Tse, M.K.3
  • 36
    • 34248577469 scopus 로고    scopus 로고
    • Synthesis of cyclopropanes via Pd(II/IV)-catalyzed reactions of Enynes
    • Welbes, L. L., Lyons, T. W., Cychosz, K. A. & Sanford, M. S. Synthesis of cyclopropanes via Pd(II/IV)-catalyzed reactions of Enynes. J. Am. Chem. Soc. 129, 5836-5837 (2007
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 5836-5837
    • Welbes, L.L.1    Lyons, T.W.2    Cychosz, K.A.3    Sanford, M.S.4
  • 37
    • 68249145558 scopus 로고    scopus 로고
    • PdII/PdIV catalytic enantioselective synthesis of Bicyclo[3.1.0]hexanes via oxidative cyclization of Enynes
    • Tsujihara, T., Takenaka, K., Onitsuka, K., Hatanaka, M. & Sasai, H. PdII/PdIV catalytic enantioselective synthesis of Bicyclo[3.1.0]hexanes via oxidative cyclization of Enynes. J. Am. Chem. Soc. 131, 3452-3453 (2009
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 3452-3453
    • Tsujihara, T.1    Takenaka, K.2    Onitsuka, K.3    Hatanaka, M.4    Sasai, H.5
  • 38
    • 84901706076 scopus 로고    scopus 로고
    • Enantioselective cycloisomerization of 1, 6-Enynes to Bicyclo[3.1.0]hexanes catalyzed by rhodium and benzoic acid
    • Masutomi, K., Noguchi, K. & Tanaka, K. Enantioselective cycloisomerization of 1, 6-Enynes to Bicyclo[3.1.0]hexanes catalyzed by rhodium and benzoic acid. J. Am. Chem. Soc. 136, 7627-7630 (2014
    • (2014) J. Am. Chem. Soc , vol.136 , pp. 7627-7630
    • Masutomi, K.1    Noguchi, K.2    Tanaka, K.3
  • 39
    • 0034654216 scopus 로고    scopus 로고
    • Proline-catalyzed direct asymmetric aldol reactions
    • List, B., Lerner, R. A. & Barbas, III C. F. Proline-catalyzed direct asymmetric aldol reactions. J. Am. Chem. Soc. 122, 2395-2396 (2000
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 2395-2396
    • List, B.1    Lerner, R.A.2    Barbas, C.F.3
  • 40
    • 0034600250 scopus 로고    scopus 로고
    • New strategies for organic catalysis: The first highly enantioselective organocatalytic diels-Alder reaction
    • Ahrendt, K. A., Borths, C. J. & MacMillan, D. W. C. New strategies for organic catalysis: the first highly enantioselective organocatalytic diels-Alder reaction. J. Am. Chem. Soc. 122, 4243-4244 (2000
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 4243-4244
    • Ahrendt, K.A.1    Borths, C.J.2    MacMillan, D.W.C.3
  • 41
    • 84879542001 scopus 로고    scopus 로고
    • New strategies for organic catalysis: Enantioselective intramolecular aldehyde a-Alkylation with simple olefins: Direct access to homo-ene products
    • Comito, R. J., Finelli, F. G. & MacMillan, D. W. C. New strategies for organic catalysis: enantioselective intramolecular aldehyde a-Alkylation with simple olefins: direct access to homo-ene products. J. Am. Chem. Soc. 135, 9358-9361 (2013
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 9358-9361
    • Comito, R.J.1    Finelli, F.G.2    MacMillan, D.W.C.3
  • 42
    • 34447533890 scopus 로고    scopus 로고
    • A simple organocatalytic enantioselective cyclopropanation of a, b-unsaturated aldehydes
    • Rios, R. et al. A simple organocatalytic enantioselective cyclopropanation of a, b-unsaturated aldehydes. Adv. Synth. Catal. 349, 1028-1032 (2007
    • (2007) Adv. Synth. Catal , vol.349 , pp. 1028-1032
    • Rios, R.1
  • 43
    • 34848814187 scopus 로고    scopus 로고
    • Organocatalytic enantioselective cascade michael-Alkylation reactions: Synthesis of chiral cyclopropanes and investigation of unexpected organocatalyzed stereoselective ring opening of cyclopropanes
    • Xie, H., Zu, L., Li, H., Wang, J. & Wang, W. Organocatalytic enantioselective cascade michael-Alkylation reactions: synthesis of chiral cyclopropanes and investigation of unexpected organocatalyzed stereoselective ring opening of cyclopropanes. J. Am. Chem. Soc. 129, 10886-10894 (2007
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 10886-10894
    • Xie, H.1    Zu, L.2    Li, H.3    Wang, J.4    Wang, W.5
  • 44
    • 44249107850 scopus 로고    scopus 로고
    • Organocatalytic asymmetric nitrocyclopropanation of a, b-unsaturated aldehydes
    • Vesely, J., Zhao, G.-L., Bartoszewicz, A. & Córdova, A. Organocatalytic asymmetric nitrocyclopropanation of a, b-unsaturated aldehydes. Tetrahedon Lett 49, 4209-4212 (2008
    • (2008) Tetrahedon Lett , vol.49 , pp. 4209-4212
    • Vesely, J.1    Zhao, G.-L.2    Bartoszewicz, A.3    Córdova, A.4
  • 45
    • 14944346768 scopus 로고    scopus 로고
    • Organocatalytic asymmetric nitrocyclopropanation of a, b-unsaturated aldehydes
    • Kunz, R. K. & MacMillan, D. W. C. Organocatalytic asymmetric nitrocyclopropanation of a, b-unsaturated aldehydes. J. Am. Chem. Soc. 127, 3240-3241 (2005
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 3240-3241
    • Kunz, R.K.1    MacMillan, D.W.C.2
  • 46
    • 84890743941 scopus 로고    scopus 로고
    • Direct a-vinylidenation of aldehydes and subsequent cascade: Gold and amine catalysts work synergistically
    • Wang, Z., Li, X. & Huang, Y. Direct a-vinylidenation of aldehydes and subsequent cascade: gold and amine catalysts work synergistically. Angew. Chem. Int. Ed. Engl. 52, 14219-14223 (2013
    • (2013) Angew. Chem. Int. Ed. Engl , vol.52 , pp. 14219-14223
    • Wang, Z.1    Li, X.2    Huang, Y.3
  • 48
    • 1842450587 scopus 로고    scopus 로고
    • Direct and enantioselective organocatalytic a-chlorination of aldehydes
    • Brochu, M. P., Brown, S. P. & MacMillan, D. W. C. Direct and enantioselective organocatalytic a-chlorination of aldehydes. J. Am. Chem. Soc. 126, 4108-4109 (2004
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 4108-4109
    • Brochu, M.P.1    Brown, S.P.2    MacMillan, D.W.C.3
  • 50
    • 20944444147 scopus 로고    scopus 로고
    • Enantioselective organocatalytic afluorination of aldehydes
    • Beeson, T. D. & MacMillan, D. W. C. Enantioselective organocatalytic afluorination of aldehydes. J. Am. Chem. Soc. 127, 8826-8828 (2005
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 8826-8828
    • Beeson, T.D.1    MacMillan, D.W.C.2
  • 51
    • 17144415210 scopus 로고    scopus 로고
    • Direct organocatalytic a-fluorination of aldehydes and ketones
    • Enders, D. & Hüttl, M. R. M. Direct organocatalytic a-fluorination of aldehydes and ketones. Synlett 6, 991-993 (2005
    • (2005) Synlett , vol.6 , pp. 991-993
    • Enders, D.1    Hüttl, M.R.M.2
  • 52
  • 53
    • 27144454544 scopus 로고    scopus 로고
    • Organocatalytic asymmetric a-bromination of aldehydes and ketones
    • Bertelsen, S. et al. Organocatalytic asymmetric a-bromination of aldehydes and ketones. Chem. Commun. 4821-4823 (2005
    • (2005) Chem. Commun , pp. 4821-4823
    • Bertelsen, S.1
  • 54
    • 41149147540 scopus 로고    scopus 로고
    • Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst
    • Kano, T., Ueda, M. & Maruoka, K. Direct asymmetric iodination of aldehydes using an axially chiral bifunctional amino alcohol catalyst. J. Am. Chem. Soc. 130, 3728-3729 (2008
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 3728-3729
    • Kano, T.1    Ueda, M.2    Maruoka, K.3
  • 55
    • 80155179849 scopus 로고    scopus 로고
    • Transforming terpene-derived aldehydes into 1, 2-epoxides via asymmetric a-chlorination: Subsequent epoxide opening with carbon nucleophiles
    • Winter, P. et al. Transforming terpene-derived aldehydes into 1, 2-epoxides via asymmetric a-chlorination: subsequent epoxide opening with carbon nucleophiles. Chem. Commun. 47, 12200-12202 (2011
    • (2011) Chem. Commun , vol.47 , pp. 12200-12202
    • Winter, P.1
  • 56
    • 84893822371 scopus 로고    scopus 로고
    • A formal, one-pot b-chlorination of primary alcohols and its utilization in the transformation of terpene feedstock and the synthesis of a c2-symmetrical terminal bis-epoxide
    • Swatschek, J., Grothues, L., Bauer, J. O., Strohmann, C. & Christmann, M. A formal, one-pot b-chlorination of primary alcohols and its utilization in the transformation of terpene feedstock and the synthesis of a c2-symmetrical terminal bis-epoxide. J. Org. Chem. 79, 976-983 (2014
    • (2014) J. Org. Chem , vol.79 , pp. 976-983
    • Swatschek, J.1    Grothues, L.2    Bauer, J.O.3    Strohmann, C.4    Christmann, M.5
  • 57
    • 29844457732 scopus 로고    scopus 로고
    • A general organocatalyst for direct a-functionalization of aldehydes: Stereoselective C-C, C-N, C-F, C-Br, and C-S bondforming reactions scope and mechanistic insights
    • Franzén, J. et al. A general organocatalyst for direct a-functionalization of aldehydes: stereoselective C-C, C-N, C-F, C-Br, and C-S bondforming reactions. scope and mechanistic insights. J. Am. Chem. Soc. 127, 18296-18304 (2005
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 18296-18304
    • Franzén, J.1
  • 58
    • 0000844109 scopus 로고    scopus 로고
    • Reductive amination of aldehydes and ketones with sodium triacetoxyborohydride studies on direct and indirect reductive amination procedures1
    • Abdel-Magid, A. F., Carson, K. G., Harris, B. D., Maryanoff, C. A. & Shah, R. D. Reductive amination of aldehydes and ketones with sodium triacetoxyborohydride. studies on direct and indirect reductive amination procedures1. J. Org. Chem. 61, 3849-3862 (1996
    • (1996) J. Org. Chem , vol.61 , pp. 3849-3862
    • Abdel-Magid, A.F.1    Carson, K.G.2    Harris, B.D.3    Maryanoff, C.A.4    Shah, R.D.5
  • 59
    • 0345391556 scopus 로고
    • The utility of phosphonate carbanions in olefin synthesis
    • Wadsworth, W. S. & Emmons, Jr W. D. The utility of phosphonate carbanions in olefin synthesis. J. Am. Chem. Soc. 83, 1733-1738 (1961
    • (1961) J. Am. Chem. Soc , vol.83 , pp. 1733-1738
    • Wadsworth, W.S.1    Emmons, W.D.2
  • 60
    • 0346688599 scopus 로고    scopus 로고
    • Further improvements of the synthesis of alkynes from aldehydes
    • Roth, G., Liepold, B., Müller, S. & Bestmann, H. J. Further improvements of the synthesis of alkynes from aldehydes. Synthesis 1, 59-62 (2004
    • (2004) Synthesis , vol.1 , pp. 59-62
    • Roth, G.1    Liepold, B.2    Müller, S.3    Bestmann, H.J.4
  • 61
    • 33947485009 scopus 로고
    • Dimethyloxosulfonium methylide ((CH3)2SOCH2) and dimethylsulfonium methylide ((CH3)2SCH2) Formation and application to organic synthesis
    • Corey, E. J. & Chaykovsky, M. Dimethyloxosulfonium methylide ((CH3)2SOCH2) and dimethylsulfonium methylide ((CH3)2SCH2). Formation and application to organic synthesis. J. Am. Chem. Soc. 87, 1353-1364 (1965
    • (1965) J. Am. Chem. Soc , vol.87 , pp. 1353-1364
    • Corey, E.J.1    Chaykovsky, M.2
  • 62
    • 33947441366 scopus 로고
    • A simple modification of the Wolff-Kishner reduction
    • Huang, M. A simple modification of the Wolff-Kishner reduction. J. Am. Chem. Soc. 68, 2487-2488 (1946
    • (1946) J. Am. Chem. Soc , vol.68 , pp. 2487-2488
    • Huang, M.1
  • 63
    • 84958613487 scopus 로고
    • Die 1, 4-Eliminierung unter Fragmentierung
    • Grob, C. A. & Baumann, W. Die 1, 4-Eliminierung unter Fragmentierung. Helv. Chim. Acta. 38, 594-610 (1955
    • (1955) Helv. Chim. Acta , vol.38 , pp. 594-610
    • Grob, C.A.1    Baumann, W.2
  • 64
    • 84857208523 scopus 로고    scopus 로고
    • Mukaiyama- Michael reactions with acrolein and methacrolein: A catalytic enantioselective synthesis of the C17-C28 fragment of pectenotoxins
    • Kemppainen, E. K., Sahoo, G., Valkonen, A. & Pihko, P. M. Mukaiyama- Michael reactions with acrolein and methacrolein: a catalytic enantioselective synthesis of the C17-C28 fragment of pectenotoxins. Org. Lett. 14, 1086-1089 (2012
    • (2012) Org. Lett , vol.14 , pp. 1086-1089
    • Kemppainen, E.K.1    Sahoo, G.2    Valkonen, A.3    Pihko, P.M.4
  • 65
    • 67649506359 scopus 로고    scopus 로고
    • Asymmetric tandem michael addition-wittig reaction to cyclohexenone annulation
    • Liu, Y.-K., Ma, C., Jiang, K., Liu, T.-Y. & Chen, Y.-C. Asymmetric tandem michael addition-wittig reaction to cyclohexenone annulation. Org. Lett. 11, 2848-2851 (2009
    • (2009) Org. Lett , vol.11 , pp. 2848-2851
    • Liu, Y.-K.1    Ma, C.2    Jiang, K.3    Liu, T.-Y.4    Chen, Y.-C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.