메뉴 건너뛰기




Volumn 531, Issue 7595, 2016, Pages 459-465

Direct synthesis of Z-alkenyl halides through catalytic cross-metathesis

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ALKENYL GROUP; BROMIDE; CHLORIDE; ETHYLENE; HALIDE; MOLYBDENUM; BIOLOGICAL PRODUCT; FLUORIDE;

EID: 84961637348     PISSN: 00280836     EISSN: 14764687     Source Type: Journal    
DOI: 10.1038/nature17396     Document Type: Article
Times cited : (152)

References (50)
  • 1
    • 84860625099 scopus 로고    scopus 로고
    • Biosynthetically intriguing chlorinated lipophilic metabolites from geographically distant tropical marine cyanobacteria
    • Nunnery J. K., et al. Biosynthetically intriguing chlorinated lipophilic metabolites from geographically distant tropical marine cyanobacteria. J. Org. Chem. 77, 4198-4208 (2012
    • (2012) J. Org. Chem , vol.77 , pp. 4198-4208
    • Nunnery, J.K.1
  • 2
    • 84879460795 scopus 로고    scopus 로고
    • Stimulators of adipogenesis from the marine sponge Xestospongia testudinaria
    • Akiyama T., et al. Stimulators of adipogenesis from the marine sponge Xestospongia testudinaria. Tetrahedron 69, 6560-6564 (2013
    • (2013) Tetrahedron , vol.69 , pp. 6560-6564
    • Akiyama, T.1
  • 3
    • 84862065162 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling: A historical contextual perspective to the 2010 Nobel Prize
    • Johansson Seechurn C. C. C., Kitching M. O., Colacot T. J., & Sniekus V. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. Angew. Chem. Int. Ed. 51, 5062-5085 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5062-5085
    • Johansson Seechurn, C.C.C.1    Kitching, M.O.2    Colacot, T.J.3    Sniekus, V.4
  • 5
    • 85027959027 scopus 로고    scopus 로고
    • Successful fluorine-containing herbicide agrochemicals
    • Fujiwara T., & O?Hagan D. Successful fluorine-containing herbicide agrochemicals. J. Fluor. Chem. 167, 16-29 (2014
    • (2014) J. Fluor. Chem , vol.167 , pp. 16-29
    • Fujiwara, T.1    Ohagan, D.2
  • 6
    • 79959421993 scopus 로고    scopus 로고
    • Organic fluorine compounds: A great opportunity for enhanced materials properties
    • Berger R., Resnati G., Metrangolo P., Weber E., & Hulliger J. Organic fluorine compounds: a great opportunity for enhanced materials properties. Chem. Soc. Rev. 40, 3496-3508 (2011
    • (2011) Chem. Soc. Rev , vol.40 , pp. 3496-3508
    • Berger, R.1    Resnati, G.2    Metrangolo, P.3    Weber, E.4    Hulliger, J.5
  • 7
    • 0023144723 scopus 로고
    • Synthesis and evaluation of mono-, di-, and trifluoroethenyl-GABA derivatives as GABA-T inhibitors
    • Kolb M., Barth J., Heydt J.-G., & Jung M. J. Synthesis and evaluation of mono-, di-, and trifluoroethenyl-GABA derivatives as GABA-T inhibitors. J. Med. Chem. 30, 267-272 (1987
    • (1987) J. Med. Chem , vol.30 , pp. 267-272
    • Kolb, M.1    Barth, J.2    Heydt, J.-G.3    Jung, M.J.4
  • 8
    • 0029964692 scopus 로고    scopus 로고
    • Unusual mechanistic difference in the activation of γ-aminobutyric acid aminotransferase by (E)-and (Z)-4-amino-6-fluoro-5-hexenoic acid
    • Silverman R. B., Bichler K. A., & Leon A. J. Unusual mechanistic difference in the activation of γ-aminobutyric acid aminotransferase by (E)-and (Z)-4-amino-6-fluoro-5-hexenoic acid. J. Am. Chem. Soc. 118, 1253-1261 (1996
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 1253-1261
    • Silverman, R.B.1    Bichler, K.A.2    Leon, A.J.3
  • 9
    • 4544303838 scopus 로고    scopus 로고
    • Fluorinated phenylcyclopropylamines as inhibitors of monoamine oxidases
    • Rosen T. C., Yoshida S., Kirk K. L., & Haufe G. Fluorinated phenylcyclopropylamines as inhibitors of monoamine oxidases. ChemBioChem 5, 1033-1043 (2004
    • (2004) ChemBioChem , vol.5 , pp. 1033-1043
    • Rosen, T.C.1    Yoshida, S.2    Kirk, K.L.3    Haufe, G.4
  • 10
    • 0038034652 scopus 로고    scopus 로고
    • Synthesis of functionalized vinylboronates via ruthenium-catalyzed cross-metathesis and subsequent conversion to vinyl halides
    • Morrill C., & Grubbs R. H. Synthesis of functionalized vinylboronates via ruthenium-catalyzed cross-metathesis and subsequent conversion to vinyl halides. J. Org. Chem. 68, 6031-6034 (2003
    • (2003) J. Org. Chem , vol.68 , pp. 6031-6034
    • Morrill, C.1    Grubbs, R.H.2
  • 11
  • 12
    • 61349086037 scopus 로고    scopus 로고
    • Convenient one-pot synthesis of (E)-β-aryl vinyl halides from benzyl bromides and dihalomethanes
    • Bull J. A., Mousseau J. J., & Charette A. B. Convenient one-pot synthesis of (E)-β-aryl vinyl halides from benzyl bromides and dihalomethanes. Org. Lett. 10, 5485-5488 (2008
    • (2008) Org. Lett , vol.10 , pp. 5485-5488
    • Bull, J.A.1    Mousseau, J.J.2    Charette, A.B.3
  • 13
    • 77955564531 scopus 로고    scopus 로고
    • Α-Selective Ni-catalyzed hydroalumination of aryl-and alkyl-substituted terminal alkynes: Practical syntheses of internal vinyl aluminums, halides, or boronates
    • Gao F., & Hoveyda A. H. α-Selective Ni-catalyzed hydroalumination of aryl-and alkyl-substituted terminal alkynes: practical syntheses of internal vinyl aluminums, halides, or boronates. J. Am. Chem. Soc. 132, 10961-10963 (2010
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 10961-10963
    • Gao, F.1    Hoveyda, A.H.2
  • 14
    • 0001647908 scopus 로고
    • A stereoselective synthesis of (Z)-1-iodo-1-alkenes
    • Stork G., & Zhao K. A stereoselective synthesis of (Z)-1-iodo-1-alkenes. Tetrahedr. Lett. 30, 2173-2174 (1989
    • (1989) Tetrahedr. Lett , vol.30 , pp. 2173-2174
    • Stork, G.1    Zhao, K.2
  • 15
    • 0027471607 scopus 로고
    • Highly cis-selective Wittig reactions employing α-heterosubstituted ylids
    • Zhang X.-P., & Schlosser M. Highly cis-selective Wittig reactions employing α-heterosubstituted ylids. Tetrahedr. Lett. 34, 1925-1928 (1993
    • (1993) Tetrahedr. Lett , vol.34 , pp. 1925-1928
    • Zhang, X.-P.1    Schlosser, M.2
  • 16
    • 80052828252 scopus 로고    scopus 로고
    • Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations
    • Crane E. A., Zabawa T. P., Farmer R. L., & Scheidt K. A. Enantioselective synthesis of (-)-exiguolide by iterative stereoselective dioxinone-directed Prins cyclizations. Angew. Chem. Int. Ed. 50, 9112-9115 (2011
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9112-9115
    • Crane, E.A.1    Zabawa, T.P.2    Farmer, R.L.3    Scheidt, K.A.4
  • 17
    • 79952577870 scopus 로고    scopus 로고
    • Stereoselective synthesis of both stereoisomers of β-fluorostyrene derivatives from a common intermediate
    • Landelle G., Turcotte-Savard M.-C., Angers L., & Paquin J. F. Stereoselective synthesis of both stereoisomers of β-fluorostyrene derivatives from a common intermediate. Org. Lett. 13, 1568-1571 (2011
    • (2011) Org. Lett , vol.13 , pp. 1568-1571
    • Landelle, G.1    Turcotte-Savard, M.-C.2    Angers, L.3    Paquin, J.F.4
  • 18
    • 21844480112 scopus 로고    scopus 로고
    • Chromium mediated stereoselective synthesis of (Z)-1-fluoro-2-alkenyl alkyl and trialkylsilyl ethers from dibromofluoromethylcarbinyl ethers
    • Nakagawa M., Saito A., Soga A., Yamamoto N., & Taguchi T. Chromium mediated stereoselective synthesis of (Z)-1-fluoro-2-alkenyl alkyl and trialkylsilyl ethers from dibromofluoromethylcarbinyl ethers. Tetrahedr. Lett. 46, 5257-5261 (2005
    • (2005) Tetrahedr. Lett , vol.46 , pp. 5257-5261
    • Nakagawa, M.1    Saito, A.2    Soga, A.3    Yamamoto, N.4    Taguchi, T.5
  • 19
    • 0034709380 scopus 로고    scopus 로고
    • Rhodium-or iridium-catalyzed trans-hydroboration of terminal alkynes, giving (Z)-1-alkenylboron compounds
    • Ohmura T., Yamamoto Y., & Miyaura N. Rhodium-or iridium-catalyzed trans-hydroboration of terminal alkynes, giving (Z)-1-alkenylboron compounds. J. Am. Chem. Soc. 122, 4990-4991 (2000
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 4990-4991
    • Ohmura, T.1    Yamamoto, Y.2    Miyaura, N.3
  • 20
    • 51549113575 scopus 로고    scopus 로고
    • Highly stereoselective synthesis of cis-alkenyl pinacolatoboronates and potassium cis-alkenyltrifluoroborates via a hydroboration/protodeboronation approach
    • Molander G. A., & Ellis N. M. Highly stereoselective synthesis of cis-alkenyl pinacolatoboronates and potassium cis-alkenyltrifluoroborates via a hydroboration/protodeboronation approach. J. Org. Chem. 73, 6841-6844 (2008
    • (2008) J. Org. Chem , vol.73 , pp. 6841-6844
    • Molander, G.A.1    Ellis, N.M.2
  • 21
    • 84876719402 scopus 로고    scopus 로고
    • Synthesis of Z-(pinacolato)allylboron and Z-(pinacolato) alkenylboron compounds through stereoselective catalytic cross-metathesis
    • Kiesewetter E. T., et al. Synthesis of Z-(pinacolato)allylboron and Z-(pinacolato) alkenylboron compounds through stereoselective catalytic cross-metathesis. J. Am. Chem. Soc. 135, 6026-6029 (2013
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 6026-6029
    • Kiesewetter, E.T.1
  • 22
    • 84906667949 scopus 로고    scopus 로고
    • Ruthenium-catalyzed Z-selective metathesis catalysts with modified cyclometalated carbene ligands
    • Bronner S. M., Herbert M. B., Patel P. R., Marx V. M., & Grubbs R. H. Ruthenium-catalyzed Z-selective metathesis catalysts with modified cyclometalated carbene ligands. Chem. Sci. 5, 4091-4098 (2014
    • (2014) Chem. Sci , vol.5 , pp. 4091-4098
    • Bronner, S.M.1    Herbert, M.B.2    Patel, P.R.3    Marx, V.M.4    Grubbs, R.H.5
  • 23
    • 0008449129 scopus 로고
    • Vinylic organoboranes 15 mercuration of 2-alkenyl-1 3, 2-benzodioxaboroles and boronic acids a convenient stereospecific procedure for the conversion of alkynes into (e)-1-halo-1-alkenes via mercuric salts
    • Brown H. C., Larock R. C., Gupta S. K., Rajagopalan S., & Bhat N. G. Vinylic organoboranes. 15. Mercuration of 2-alkenyl-1, 3, 2-benzodioxaboroles and boronic acids. A convenient stereospecific procedure for the conversion of alkynes into (E)-1-halo-1-alkenes via mercuric salts. J. Org. Chem. 54, 6079-6084 (1989
    • (1989) J. Org. Chem , vol.54 , pp. 6079-6084
    • Brown, H.C.1    Larock, R.C.2    Gupta, S.K.3    Rajagopalan, S.4    Bhat, N.G.5
  • 24
    • 0030032996 scopus 로고    scopus 로고
    • Mild conversion of alkenyl boronic acids to alkenyl halides with halosuccinimides
    • Petasis N. A., & Zavialov I. A. Mild conversion of alkenyl boronic acids to alkenyl halides with halosuccinimides. Tetrahedr. Lett. 37, 567-570 (1996
    • (1996) Tetrahedr. Lett , vol.37 , pp. 567-570
    • Petasis, N.A.1    Zavialov, I.A.2
  • 25
    • 0347784942 scopus 로고
    • Oxidation of thioesters to sulfoxides by iodine II catalytic role of some carboxylic acid anions
    • Gensch K. H., Pitman I. H., & Higuchi T. Oxidation of thioesters to sulfoxides by iodine. II. Catalytic role of some carboxylic acid anions. J. Am. Chem. Soc. 90, 2096-2104 (1968
    • (1968) J. Am. Chem. Soc , vol.90 , pp. 2096-2104
    • Gensch, K.H.1    Pitman, I.H.2    Higuchi, T.3
  • 27
    • 84912551734 scopus 로고    scopus 로고
    • Catalytic Z-selective cross-meta thesis in complex molecule synthesis: A convergent stereoselective route to disorazole C1
    • Speed A. W. H., Mann S. J., Obrien R. V., Schrock R. R., & Hoveyda A. H. Catalytic Z-selective cross-metathesis in complex molecule synthesis: a convergent stereoselective route to disorazole C1. J. Am. Chem. Soc. 136, 16136-16139 (2014
    • (2014) J. Am. Chem. Soc , vol.136 , pp. 16136-16139
    • Speed, A.W.H.1    Mann, S.J.2    Obrien, R.V.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 28
    • 80054865601 scopus 로고    scopus 로고
    • Anti-inflammatory effects of fatty acids isolated from Chromolaena odorata
    • Hanh T. T. H., Hang D. T. T., Minh C. V., & Dat N. T. Anti-inflammatory effects of fatty acids isolated from Chromolaena odorata. Asian Pac. J. Trop. Med. 4, 760-763 (2011
    • (2011) Asian Pac. J. Trop. Med , vol.4 , pp. 760-763
    • Hanh, T.T.H.1    Hang, D.T.T.2    Minh, C.V.3    Dat, N.T.4
  • 29
    • 23044484321 scopus 로고    scopus 로고
    • First stereoselective syntheses of (-)-siphonodiol and (-)-tetrahydrosiphonodiol, bioactive polyacetylenes from marine sponges
    • López S., Fernández-Trillo F., Midón P., Castedo L., & Saá C. First stereoselective syntheses of (-)-siphonodiol and (-)-tetrahydrosiphonodiol, bioactive polyacetylenes from marine sponges. J. Org. Chem. 70, 6346-6352 (2005
    • (2005) J. Org. Chem , vol.70 , pp. 6346-6352
    • López, S.1    Fernández-Trillo, F.2    Midón, P.3    Castedo, L.4    Saá, C.5
  • 30
    • 84899018688 scopus 로고    scopus 로고
    • Late-stage fluorination: From fundamentals to application
    • Campbell M. G., & Ritter T. Late-stage fluorination: from fundamentals to application. Org. Process Res. Dev. 18, 474-480 (2014
    • (2014) Org. Process Res. Dev , vol.18 , pp. 474-480
    • Campbell, M.G.1    Ritter, T.2
  • 31
    • 0036784042 scopus 로고    scopus 로고
    • Molecular basis of pimarane compounds as novel activators of large-conductance Ca2+-activated channel α-subunit
    • Imaizumi Y., et al. Molecular basis of pimarane compounds as novel activators of large-conductance Ca2+-activated channel α-subunit. Mol. Pharmacol. 62, 836-846 (2002
    • (2002) Mol. Pharmacol , vol.62 , pp. 836-846
    • Imaizumi, Y.1
  • 32
    • 34347267209 scopus 로고    scopus 로고
    • Olefin metathesis reactions with vinyl halides: Formation observation interception and fate of the ruthenium-monohalomethylidene moiety
    • Macnaughtan M. L., Johnson M. J. A., & Kampf J. W. Olefin metathesis reactions with vinyl halides: formation, observation, interception, and fate of the ruthenium-monohalomethylidene moiety. J. Am. Chem. Soc. 129, 7708-7709 (2007
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 7708-7709
    • Macnaughtan, M.L.1    Johnson, M.J.A.2    Kampf, J.W.3
  • 34
    • 66149131397 scopus 로고    scopus 로고
    • Cross-metathesis of vinyl halides scope and limitations of rutheniumbased catalysts
    • Macnaughtan M. L., Gary J. B., Gerlach D. L., Johnson M. J. A., & Kamf J. W. Cross-metathesis of vinyl halides. Scope and limitations of rutheniumbased catalysts. Organometallics 28, 2880-2887 (2009
    • (2009) Organometallics , vol.28 , pp. 2880-2887
    • Macnaughtan, M.L.1    Gary, J.B.2    Gerlach, D.L.3    Johnson, M.J.A.4    Kamf, J.W.5
  • 35
    • 79953031273 scopus 로고    scopus 로고
    • Catalytic Z-selective olefin metathesis for natural product synthesis
    • Meek S. J., Obrien R. V., Llaveria J., Schrock R. R., & Hoveyda A. H. Catalytic Z-selective olefin metathesis for natural product synthesis. Nature 471, 461-466 (2011
    • (2011) Nature , vol.471 , pp. 461-466
    • Meek, S.J.1    Obrien, R.V.2    Llaveria, J.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 36
    • 79959245404 scopus 로고    scopus 로고
    • Bond energies in models of the Schrock metathesis catalyst
    • Vasiliu M., Li S., Arduengo A. J. III, & Dixon D. A. Bond energies in models of the Schrock metathesis catalyst. J. Phys. Chem. C 115, 12106-12120 (2011
    • (2011) J. Phys. Chem. C , vol.115 , pp. 12106-12120
    • Vasiliu, M.1    Li, S.2    Arduengo, A.J.3    Dixon, D.A.4
  • 37
    • 84873815391 scopus 로고    scopus 로고
    • Highly active ruthenium metathesis catalysts exhibiting unprecedented activity and Z selectivity
    • Rosebrugh L. E., Herbert M. B., Marx V. M., Keitz B. K., & Grubbs R. H. Highly active ruthenium metathesis catalysts exhibiting unprecedented activity and Z selectivity. J. Am. Chem. Soc. 135, 1276-1279 (2013
    • (2013) J. Am. Chem. Soc , vol.135 , pp. 1276-1279
    • Rosebrugh, L.E.1    Herbert, M.B.2    Marx, V.M.3    Keitz, B.K.4    Grubbs, R.H.5
  • 38
    • 84923197587 scopus 로고    scopus 로고
    • High-value alcohols and higher-oxidation-state compounds by catalytic Z-selective cross-metathesis
    • Koh M. J., et al. High-value alcohols and higher-oxidation-state compounds by catalytic Z-selective cross-metathesis. Nature 517, 181-186 (2015
    • (2015) Nature , vol.517 , pp. 181-186
    • Koh, M.J.1
  • 39
    • 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
  • 41
    • 79957681266 scopus 로고    scopus 로고
    • Highly selective methods for synthesis of internal (α-) vinylboronates through efficient nhc-cu-catalyzed hydroboration of terminal alkynes utility in synthesis and mechanistic basis for selectivity
    • Jang H., Zhugralin A. R., Lee Y., & Hoveyda A. H. Highly selective methods for synthesis of internal (α-) vinylboronates through efficient NHC-Cu-catalyzed hydroboration of terminal alkynes. Utility in synthesis and mechanistic basis for selectivity. J. Am. Chem. Soc. 133, 7859-7871 (2011
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 7859-7871
    • Jang, H.1    Zhugralin, A.R.2    Lee, Y.3    Hoveyda, A.H.4
  • 42
    • 84902089766 scopus 로고    scopus 로고
    • Evolution of catalytic enantioselective olefin meta thesis: From ancillary transformation to purveyor of stereochemical identity
    • Hoveyda A. H. Evolution of catalytic enantioselective olefin metathesis: from ancillary transformation to purveyor of stereochemical identity. J. Org. Chem. 79, 4763-4792 (2014
    • (2014) J. Org. Chem , vol.79 , pp. 4763-4792
    • Hoveyda, A.H.1
  • 43
    • 84921797141 scopus 로고    scopus 로고
    • Olefin metathesis reactions with fluorinated substrates, catalysts, and solvents
    • Fustero S., Simón-Fuentes A., Barrio P., & Haufe G. Olefin metathesis reactions with fluorinated substrates, catalysts, and solvents. Chem. Rev. 115, 871-930 (2015
    • (2015) Chem. Rev , vol.115 , pp. 871-930
    • Fustero, S.1    Simón-Fuentes, A.2    Barrio, P.3    Haufe, G.4
  • 44
    • 84914178348 scopus 로고    scopus 로고
    • Preparation of macrocyclic Z-enoates and (E, Z)-or (Z, E)-dienoates through catalytic stereoselective ring-closing metathesis
    • Zhang H., Yu E. C., Torker S., Schrock R. R., & Hoveyda A. H. Preparation of macrocyclic Z-enoates and (E, Z)-or (Z, E)-dienoates through catalytic stereoselective ring-closing metathesis. J. Am. Chem. Soc. 136, 16493-16496 (2014
    • (2014) J. Am. Chem. Soc , vol.136 , pp. 16493-16496
    • Zhang, H.1    Yu, E.C.2    Torker, S.3    Schrock, R.R.4    Hoveyda, A.H.5
  • 45
    • 34250705242 scopus 로고    scopus 로고
    • Chiral N-heterocyclic carbenes in natural product syn thesis: Application of Ru-catalyzed asymmetric ring-opening/cross-metathesis and Cu-catalyzed allylic alkylation to total synthesis of baconipyrone C
    • Gillingham D. G., & Hoveyda A. H. Chiral N-heterocyclic carbenes in natural product synthesis: application of Ru-catalyzed asymmetric ring-opening/cross-metathesis and Cu-catalyzed allylic alkylation to total synthesis of baconipyrone C. Angew. Chem. Int. Ed. 46, 3860-3864 (2007
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 3860-3864
    • Gillingham, D.G.1    Hoveyda, A.H.2
  • 46
    • 79551531085 scopus 로고    scopus 로고
    • Impact of second-generation anti-psychotics and perphenazine on depressive symptoms in a randomized trial for chronic schizophrenia
    • Addington D. E., et al. Impact of second-generation anti-psychotics and perphenazine on depressive symptoms in a randomized trial for chronic schizophrenia. J. Clin. Psychiatry 72, 75-80 (2011
    • (2011) J. Clin. Psychiatry , vol.72 , pp. 75-80
    • Addington, D.E.1
  • 48
    • 67649467487 scopus 로고    scopus 로고
    • Fluorination of boronic acids mediated by silver(I) triflate
    • Furuya T., & Ritter T. Fluorination of boronic acids mediated by silver(I) triflate. Org. Lett. 11, 2860-2863 (2009
    • (2009) Org. Lett , vol.11 , pp. 2860-2863
    • Furuya, T.1    Ritter, T.2
  • 49
    • 0021162058 scopus 로고
    • Alkaline degradation and determination by high-performance liquid chromatography
    • Haginaka J., Yasuda H., Uno T., & Nakagawa T. Alkaline degradation and determination by high-performance liquid chromatography. Chem. Pharm. Bull. 32, 2752-2758 (1984
    • (1984) Chem. Pharm. Bull , vol.32 , pp. 2752-2758
    • Haginaka, J.1    Yasuda, H.2    Uno, T.3    Nakagawa, T.4
  • 50
    • 84883199606 scopus 로고    scopus 로고
    • High oxidation state molybdenum imido heteroatomsubstituted alkyliene complexes
    • Townsend E. M., et al. High oxidation state molybdenum imido heteroatomsubstituted alkyliene complexes. Organometallics 32, 4612-4617 (2013
    • (2013) Organometallics , vol.32 , pp. 4612-4617
    • Townsend, E.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.