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Volumn 49, Issue 3, 2009, Pages 377-384

Stereoselective synthesis of tetrasubstituted olefins via palladium-catalyzed three-component coupling of aryl iodides, internal alkynes, and arylboronic acids in supercritical carbon dioxide

Author keywords

Palladium catalyzed; Supercritical carbon dioxide; Tetrasubstituted olefins; Three component coupling

Indexed keywords

ARYL IODIDES; ARYLBORONIC ACIDS; ENVIRONMENTAL-FRIENDLY; INTERNAL ALKYNES; OPTIMIZED REACTION CONDITIONS; STEREO-SELECTIVE SYNTHESIS; SUPERCRITICAL CARBON DIOXIDE; TETRASUBSTITUTED OLEFINS; THREE-COMPONENT COUPLING;

EID: 65649091037     PISSN: 08968446     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.supflu.2009.02.003     Document Type: Article
Times cited : (20)

References (47)
  • 1
    • 33846799213 scopus 로고    scopus 로고
    • Total syntheses of durgamone, nakorone, and abudinol B via biomimetic oxa- and carbacyclizations
    • Tong R., Valentine J.C., McDonald F.E., Cao R., Fang X., and Hardcastle K.I. Total syntheses of durgamone, nakorone, and abudinol B via biomimetic oxa- and carbacyclizations. J. Am. Chem. Soc. 129 (2007) 1050-1051
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1050-1051
    • Tong, R.1    Valentine, J.C.2    McDonald, F.E.3    Cao, R.4    Fang, X.5    Hardcastle, K.I.6
  • 2
    • 33646180381 scopus 로고    scopus 로고
    • Racemic and chiral sulfoxides as potential prodrugs of the COX-2 inhibitors Vioxx and Arcoxia
    • Caturla F., Amat M., Reinoso R.F., Cordoba M., and Warrello G. Racemic and chiral sulfoxides as potential prodrugs of the COX-2 inhibitors Vioxx and Arcoxia. Bioorg. Med. Chem. Lett. 16 (2006) 3209-3212
    • (2006) Bioorg. Med. Chem. Lett. , vol.16 , pp. 3209-3212
    • Caturla, F.1    Amat, M.2    Reinoso, R.F.3    Cordoba, M.4    Warrello, G.5
  • 3
    • 33646455863 scopus 로고    scopus 로고
    • Cyclocarbopalladation of alkynes: a stereoselective method for preparing dibenzoxapine containing tetrasubstituted exocyclic alkenes
    • Yu H., Richey R.N., Carson M.W., and Coghlan M.J. Cyclocarbopalladation of alkynes: a stereoselective method for preparing dibenzoxapine containing tetrasubstituted exocyclic alkenes. Org. Lett. 8 (2006) 1685-1688
    • (2006) Org. Lett. , vol.8 , pp. 1685-1688
    • Yu, H.1    Richey, R.N.2    Carson, M.W.3    Coghlan, M.J.4
  • 4
    • 36849088075 scopus 로고    scopus 로고
    • Stereocontrolled synthesis of tetrasubstituted olefins
    • Flynn A.B., and Ogilvie W.W. Stereocontrolled synthesis of tetrasubstituted olefins. Chem. Rev. 107 (2007) 4698-4745
    • (2007) Chem. Rev. , vol.107 , pp. 4698-4745
    • Flynn, A.B.1    Ogilvie, W.W.2
  • 5
    • 39649113865 scopus 로고    scopus 로고
    • Alkynes as stille reaction pseudohalides: gold- and palladium-cocatalyzed synthesis of tri- and tetra-substituted olefins
    • Shi Y., Peterson S.M., Haberaecker III W.W., and Blum S.A. Alkynes as stille reaction pseudohalides: gold- and palladium-cocatalyzed synthesis of tri- and tetra-substituted olefins. J. Am. Chem. Soc. 130 (2008) 2168-2169
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 2168-2169
    • Shi, Y.1    Peterson, S.M.2    Haberaecker III, W.W.3    Blum, S.A.4
  • 6
    • 34547194244 scopus 로고    scopus 로고
    • Cationic Pd(II)-catalyzed enantioselective cyclization of aroylmethyl 2-alkynoates initiated by carbopalladation of alkynes with arylboronic acids
    • Song J., Shen Q., Xu F., and Lu X. Cationic Pd(II)-catalyzed enantioselective cyclization of aroylmethyl 2-alkynoates initiated by carbopalladation of alkynes with arylboronic acids. Org. Lett. 9 (2007) 2947-2950
    • (2007) Org. Lett. , vol.9 , pp. 2947-2950
    • Song, J.1    Shen, Q.2    Xu, F.3    Lu, X.4
  • 8
    • 13444301240 scopus 로고    scopus 로고
    • Synthesis of tetrasubstituted olefins by Pd-catalyzed addition of arylboronic acids to internal alkynes
    • Zhou C., and Larock R.C. Synthesis of tetrasubstituted olefins by Pd-catalyzed addition of arylboronic acids to internal alkynes. Org. Lett. 7 (2005) 259-262
    • (2005) Org. Lett. , vol.7 , pp. 259-262
    • Zhou, C.1    Larock, R.C.2
  • 9
    • 37249032342 scopus 로고    scopus 로고
    • A highly stereoselective TMSOTf-mediated catalytic carbocupration of alkynoates
    • Mueller A.J., and Jennings M.P. A highly stereoselective TMSOTf-mediated catalytic carbocupration of alkynoates. Org. Lett. 9 (2007) 5327-5329
    • (2007) Org. Lett. , vol.9 , pp. 5327-5329
    • Mueller, A.J.1    Jennings, M.P.2
  • 10
    • 51649120855 scopus 로고    scopus 로고
    • An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes
    • Carson M.W., Giese M.W., and Coghlan M.J. An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes. Org. Lett. 10 (2008) 2701-2704
    • (2008) Org. Lett. , vol.10 , pp. 2701-2704
    • Carson, M.W.1    Giese, M.W.2    Coghlan, M.J.3
  • 11
    • 1642288600 scopus 로고    scopus 로고
    • Highly regio- and stereoselective carbostannylation reaction of fluorine-containing internal acetylenes with allylstannanes
    • Konno T., Takehana T., Chae J., Ishihara T., and Yamanaka H. Highly regio- and stereoselective carbostannylation reaction of fluorine-containing internal acetylenes with allylstannanes. J. Org. Chem. 69 (2004) 2188-2190
    • (2004) J. Org. Chem. , vol.69 , pp. 2188-2190
    • Konno, T.1    Takehana, T.2    Chae, J.3    Ishihara, T.4    Yamanaka, H.5
  • 12
    • 34247496363 scopus 로고    scopus 로고
    • Chromium-catalyzed arylmagnesiation of alkynes
    • Murakami K., Ohmiya H., Yorimitsu H., and Oshima K. Chromium-catalyzed arylmagnesiation of alkynes. Org. Lett. 9 (2007) 1569-1571
    • (2007) Org. Lett. , vol.9 , pp. 1569-1571
    • Murakami, K.1    Ohmiya, H.2    Yorimitsu, H.3    Oshima, K.4
  • 13
    • 0345293203 scopus 로고    scopus 로고
    • Diversity-oriented synthesis of tamoxifen-type tetrasubstituted olefins
    • Itami K., Kamei T., and Yoshida J. Diversity-oriented synthesis of tamoxifen-type tetrasubstituted olefins. J. Am. Chem. Soc. 125 (2003) 14670-14671
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 14670-14671
    • Itami, K.1    Kamei, T.2    Yoshida, J.3
  • 14
    • 0346256824 scopus 로고    scopus 로고
    • Transformation of β-chalcogeno alkenylboranes into tetrasubstituted olefins
    • Gerard J., and Hevesi L. Transformation of β-chalcogeno alkenylboranes into tetrasubstituted olefins. Tetrahedron 60 (2004) 367-381
    • (2004) Tetrahedron , vol.60 , pp. 367-381
    • Gerard, J.1    Hevesi, L.2
  • 15
    • 33644506153 scopus 로고    scopus 로고
    • An efficient CuI-promoted synthesis of tri- and tetrasubstituted alkenes using organozinc species
    • Xue S., He L., Liu Y.-K., Han K.-Z., and Guo Q.-X. An efficient CuI-promoted synthesis of tri- and tetrasubstituted alkenes using organozinc species. Synthesis (2006) 666-674
    • (2006) Synthesis , pp. 666-674
    • Xue, S.1    He, L.2    Liu, Y.-K.3    Han, K.-Z.4    Guo, Q.-X.5
  • 17
    • 0037031622 scopus 로고    scopus 로고
    • Electrotelluration: a new approach to tri- and tetrasubstituted alkenes
    • Marino J.P., and Nguyen H.N. Electrotelluration: a new approach to tri- and tetrasubstituted alkenes. J. Org. Chem. 67 (2002) 6291-6296
    • (2002) J. Org. Chem. , vol.67 , pp. 6291-6296
    • Marino, J.P.1    Nguyen, H.N.2
  • 18
    • 33845528747 scopus 로고    scopus 로고
    • Carbolithiation of diphenylacetylene as a stereoselective route to (Z)-tamoxifen and related tetrasubstituted olefins
    • McKinley N.F., and O'Shea D.F. Carbolithiation of diphenylacetylene as a stereoselective route to (Z)-tamoxifen and related tetrasubstituted olefins. J. Org. Chem. 71 (2006) 9552-9555
    • (2006) J. Org. Chem. , vol.71 , pp. 9552-9555
    • McKinley, N.F.1    O'Shea, D.F.2
  • 19
    • 48249089654 scopus 로고    scopus 로고
    • Dehydrogenative cyclocondensation of aldehydes, alkynes, and dialkylsilanes
    • Baxter R.D., and Montgomery J. Dehydrogenative cyclocondensation of aldehydes, alkynes, and dialkylsilanes. J. Am. Chem. Soc. 130 (2008) 9662-9663
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9662-9663
    • Baxter, R.D.1    Montgomery, J.2
  • 20
    • 34247847728 scopus 로고    scopus 로고
    • Rh(I)-catalyzed carbonylative cyclization reactions of alkynes with 2-bromophenylboronic acids leading to indenones
    • Harada Y., Nakanishi J., Fujihara H., Tobisu M., Fukumoto Y., and Chatani N. Rh(I)-catalyzed carbonylative cyclization reactions of alkynes with 2-bromophenylboronic acids leading to indenones. J. Am. Chem. Soc. 129 (2007) 5766-5771
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5766-5771
    • Harada, Y.1    Nakanishi, J.2    Fujihara, H.3    Tobisu, M.4    Fukumoto, Y.5    Chatani, N.6
  • 21
    • 0021856564 scopus 로고
    • Stereospecific synthesis of (Z)-tamoxifen via carbometalation of alkynylsilanes
    • Miller R.B., and Al-Hassan M.I. Stereospecific synthesis of (Z)-tamoxifen via carbometalation of alkynylsilanes. J. Org. Chem. 50 (1985) 2121-2123
    • (1985) J. Org. Chem. , vol.50 , pp. 2121-2123
    • Miller, R.B.1    Al-Hassan, M.I.2
  • 22
    • 33646379585 scopus 로고    scopus 로고
    • Nickel-catalyzed cross-coupling reaction of niobium(III)-alkyne complexes with aryl iodides
    • Obora Y., Kimura M., Ohtake T., Tokunaga M., and Tsuji Y. Nickel-catalyzed cross-coupling reaction of niobium(III)-alkyne complexes with aryl iodides. Organometallics 25 (2006) 2097-2100
    • (2006) Organometallics , vol.25 , pp. 2097-2100
    • Obora, Y.1    Kimura, M.2    Ohtake, T.3    Tokunaga, M.4    Tsuji, Y.5
  • 23
    • 0344099385 scopus 로고    scopus 로고
    • Cross-coupling reaction of thermally stable titanium(II)-alkyne complexes with aryl halides catalysed by a nickel complex
    • Obora Y., Moriya H., Tokunaga M., and Tsuji Y. Cross-coupling reaction of thermally stable titanium(II)-alkyne complexes with aryl halides catalysed by a nickel complex. Chem. Commun. (2003) 2820-2821
    • (2003) Chem. Commun. , pp. 2820-2821
    • Obora, Y.1    Moriya, H.2    Tokunaga, M.3    Tsuji, Y.4
  • 24
    • 38349179753 scopus 로고    scopus 로고
    • Platinum-catalyzed regio- and stereoselective arylthiolation of internal alkynes
    • Yamashita F., Kuniyasu H., Terao J., and Kambe N. Platinum-catalyzed regio- and stereoselective arylthiolation of internal alkynes. Org. Lett. 10 (2008) 101-104
    • (2008) Org. Lett. , vol.10 , pp. 101-104
    • Yamashita, F.1    Kuniyasu, H.2    Terao, J.3    Kambe, N.4
  • 25
    • 36849083534 scopus 로고    scopus 로고
    • Stereoselective synthesis of (E)- and (Z)-fluoroalkenylboronates using 2-fluoroalkylideneiodonium ylides generated from (2-fluoro-1-alkenyl)iodonium salts
    • Guan T., Yoshida M., and Hara S. Stereoselective synthesis of (E)- and (Z)-fluoroalkenylboronates using 2-fluoroalkylideneiodonium ylides generated from (2-fluoro-1-alkenyl)iodonium salts. J. Org. Chem. 71 (2007) 9617-9621
    • (2007) J. Org. Chem. , vol.71 , pp. 9617-9621
    • Guan, T.1    Yoshida, M.2    Hara, S.3
  • 26
    • 33846111706 scopus 로고    scopus 로고
    • Synthesis of indenes by the transition metal-mediated carboannulation of alkynes
    • Zhang D., Liu Z., Yum E.K., and Larock R.C. Synthesis of indenes by the transition metal-mediated carboannulation of alkynes. J. Org. Chem. 72 (2007) 251-262
    • (2007) J. Org. Chem. , vol.72 , pp. 251-262
    • Zhang, D.1    Liu, Z.2    Yum, E.K.3    Larock, R.C.4
  • 27
    • 33947219004 scopus 로고    scopus 로고
    • Palladium-catalyzed C-P coupling reactions between vinyl triflates and phosphine-boranes: efficient access to vinylphosphine-boranes
    • Julienne D., Lohier J., Delacroix O., and Gaumont A. Palladium-catalyzed C-P coupling reactions between vinyl triflates and phosphine-boranes: efficient access to vinylphosphine-boranes. J. Org. Chem. 72 (2007) 2247-2250
    • (2007) J. Org. Chem. , vol.72 , pp. 2247-2250
    • Julienne, D.1    Lohier, J.2    Delacroix, O.3    Gaumont, A.4
  • 29
    • 33745700301 scopus 로고    scopus 로고
    • Synthesis of substituted carbazoles, indoles, and dibenzofurans by vinylic to aryl palladium migration
    • Zhao J., and Larock R.C. Synthesis of substituted carbazoles, indoles, and dibenzofurans by vinylic to aryl palladium migration. J. Org. Chem. 71 (2006) 5340-5348
    • (2006) J. Org. Chem. , vol.71 , pp. 5340-5348
    • Zhao, J.1    Larock, R.C.2
  • 30
    • 0038608340 scopus 로고    scopus 로고
    • An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins
    • Zhou C., Emrich D.E., and Larock R.C. An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins. Org. Lett. 5 (2003) 1579-1582
    • (2003) Org. Lett. , vol.5 , pp. 1579-1582
    • Zhou, C.1    Emrich, D.E.2    Larock, R.C.3
  • 31
    • 18744378312 scopus 로고    scopus 로고
    • Regio- and stereoselective route to tetrasubstituted olefins by the palladium-catalyzed three-component coupling of aryl iodides, internal alkynes, and arylboronic acids
    • Zhou C., and Larock R.C. Regio- and stereoselective route to tetrasubstituted olefins by the palladium-catalyzed three-component coupling of aryl iodides, internal alkynes, and arylboronic acids. J. Org. Chem. 70 (2005) 3765-3777
    • (2005) J. Org. Chem. , vol.70 , pp. 3765-3777
    • Zhou, C.1    Larock, R.C.2
  • 32
    • 0037191619 scopus 로고    scopus 로고
    • Stereospecific synthesis of highly substituted skipped dienes through multifunctional palladium catalysis
    • Thadani A.N., and Rawal V.H. Stereospecific synthesis of highly substituted skipped dienes through multifunctional palladium catalysis. Org. Lett. 4 (2002) 4317-4320
    • (2002) Org. Lett. , vol.4 , pp. 4317-4320
    • Thadani, A.N.1    Rawal, V.H.2
  • 33
    • 4944233291 scopus 로고    scopus 로고
    • Synthesis of highly substituted 1,3-butadienes by palladium-catalyzed arylation of internal alkynes
    • Satoh T., Ogino S., Miura M., and Nomura M. Synthesis of highly substituted 1,3-butadienes by palladium-catalyzed arylation of internal alkynes. Angew. Chem. Int. Ed. 43 (2004) 5063-5065
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5063-5065
    • Satoh, T.1    Ogino, S.2    Miura, M.3    Nomura, M.4
  • 35
    • 0001185004 scopus 로고    scopus 로고
    • Homogeneous catalysis in supercritical fluids
    • Jessop P.G., Kariya T., and Noyori R. Homogeneous catalysis in supercritical fluids. Chem. Rev. 99 (1999) 475-493
    • (1999) Chem. Rev. , vol.99 , pp. 475-493
    • Jessop, P.G.1    Kariya, T.2    Noyori, R.3
  • 36
    • 14044250857 scopus 로고    scopus 로고
    • Transition metal-catalyzed organic reactions in supercritical carbon dioxide
    • Jiang H.F. Transition metal-catalyzed organic reactions in supercritical carbon dioxide. Curr. Org. Chem. 9 (2005) 289-297
    • (2005) Curr. Org. Chem. , vol.9 , pp. 289-297
    • Jiang, H.F.1
  • 37
    • 23844544959 scopus 로고    scopus 로고
    • PS-BQ: an efficient polymer-supported cocatalyst for the wacker reaction in supercritical carbon dioxide
    • Wang Z.Y., Jiang H.F., Qi C.R., Wang Y.G., Dong Y.S., and Liu H.L. PS-BQ: an efficient polymer-supported cocatalyst for the wacker reaction in supercritical carbon dioxide. Green Chem. 7 (2005) 582-585
    • (2005) Green Chem. , vol.7 , pp. 582-585
    • Wang, Z.Y.1    Jiang, H.F.2    Qi, C.R.3    Wang, Y.G.4    Dong, Y.S.5    Liu, H.L.6
  • 38
    • 33645957688 scopus 로고    scopus 로고
    • Cu(II)-promoted oxidative homocoupling reaction of terminal alkynes in supercritical carbon dioxide
    • Jiang H.F., Tang J.Y., Wang A.Z., Deng G.H., and Yang S.R. Cu(II)-promoted oxidative homocoupling reaction of terminal alkynes in supercritical carbon dioxide. Synthesis (2006) 1155-1161
    • (2006) Synthesis , pp. 1155-1161
    • Jiang, H.F.1    Tang, J.Y.2    Wang, A.Z.3    Deng, G.H.4    Yang, S.R.5
  • 39
    • 33748179720 scopus 로고    scopus 로고
    • Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups in supercritical carbon dioxide: selective control and mechanism
    • Wang Z.Y., Jiang H.F., Ouyang X.Y., Qi C.R., and Yang S.R. Pd(II)-catalyzed acetalization of terminal olefins with electron-withdrawing groups in supercritical carbon dioxide: selective control and mechanism. Tetrahedron 62 (2006) 9846-9854
    • (2006) Tetrahedron , vol.62 , pp. 9846-9854
    • Wang, Z.Y.1    Jiang, H.F.2    Ouyang, X.Y.3    Qi, C.R.4    Yang, S.R.5
  • 40
    • 34250320478 scopus 로고    scopus 로고
    • Copper-catalyzed cross-coupling reactions of bromoalkynols with terminal alkynes in supercritical carbon dioxide
    • Jiang H.F., and Wang A.Z. Copper-catalyzed cross-coupling reactions of bromoalkynols with terminal alkynes in supercritical carbon dioxide. Synthesis (2007) 1649-1654
    • (2007) Synthesis , pp. 1649-1654
    • Jiang, H.F.1    Wang, A.Z.2
  • 41
    • 34748904247 scopus 로고    scopus 로고
    • Palladium-catalyzed C-N bond activation: the synthesis of β-amino acid derivatives from triethylamine and acrylates
    • Zou B., Jiang H.F., and Wang Z.Y. Palladium-catalyzed C-N bond activation: the synthesis of β-amino acid derivatives from triethylamine and acrylates. Eur. J. Org. Chem. (2007) 4600-4604
    • (2007) Eur. J. Org. Chem. , pp. 4600-4604
    • Zou, B.1    Jiang, H.F.2    Wang, Z.Y.3
  • 42
    • 0033532601 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed oxidation of acrylate esters to acetals in supercritical carbon dioxide
    • Jia L.Q., Jiang H.F., and Li J.H. Palladium(II)-catalyzed oxidation of acrylate esters to acetals in supercritical carbon dioxide. Chem. Commun. (1999) 985-986
    • (1999) Chem. Commun. , pp. 985-986
    • Jia, L.Q.1    Jiang, H.F.2    Li, J.H.3
  • 43
    • 35348838961 scopus 로고    scopus 로고
    • Practical synthesis of unsymmetrical tetraarylethylenes and their application for the preparation of [triphenylethylene-spacer- triphenylethylene] triads
    • Banerjee M., Emond S.J., Lindeman S.V., and Rathore R. Practical synthesis of unsymmetrical tetraarylethylenes and their application for the preparation of [triphenylethylene-spacer- triphenylethylene] triads. J. Org. Chem. 72 (2007) 8054-8061
    • (2007) J. Org. Chem. , vol.72 , pp. 8054-8061
    • Banerjee, M.1    Emond, S.J.2    Lindeman, S.V.3    Rathore, R.4
  • 44
    • 0037353477 scopus 로고    scopus 로고
    • Synthesis of polysubstituted alkenes by Heck vinylation or Suzuki cross-coupling reactions in the presence of a tetraphosphane-palladium catalyst
    • Berthiol F., Doucet H., and Santelli M. Synthesis of polysubstituted alkenes by Heck vinylation or Suzuki cross-coupling reactions in the presence of a tetraphosphane-palladium catalyst. Eur. J. Org. Chem. (2003) 1091-1096
    • (2003) Eur. J. Org. Chem. , pp. 1091-1096
    • Berthiol, F.1    Doucet, H.2    Santelli, M.3
  • 45
    • 0343180564 scopus 로고
    • Photochemical reactions of triarylmethyl peroxides(II) α- and β-naphthyldiphenylmethyl peroxide
    • Neckers D.C., Linden S., Taliano R.J., Williams B.L., and Zakrzewski A. Photochemical reactions of triarylmethyl peroxides(II) α- and β-naphthyldiphenylmethyl peroxide. Tetrahedron Lett. 29 (1988) 3029-3032
    • (1988) Tetrahedron Lett. , vol.29 , pp. 3029-3032
    • Neckers, D.C.1    Linden, S.2    Taliano, R.J.3    Williams, B.L.4    Zakrzewski, A.5
  • 46
    • 0042531833 scopus 로고    scopus 로고
    • Toward waste-free production of Heck products with a catalytic palladium system under oxygen
    • Dams M., De Vos D.E., Celen S., and Jacobs P.A. Toward waste-free production of Heck products with a catalytic palladium system under oxygen. Angew. Chem. Int. Ed. 42 (2003) 3512-3515
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 3512-3515
    • Dams, M.1    De Vos, D.E.2    Celen, S.3    Jacobs, P.A.4
  • 47
    • 33845949018 scopus 로고    scopus 로고
    • Insights into the general and efficient cross McMurry reactions between ketones
    • Duan X.F., Zeng J., Lue J.W., and Zhang Z.B. Insights into the general and efficient cross McMurry reactions between ketones. J. Org. Chem. 71 (2006) 9873-9876
    • (2006) J. Org. Chem. , vol.71 , pp. 9873-9876
    • Duan, X.F.1    Zeng, J.2    Lue, J.W.3    Zhang, Z.B.4


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