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Volumn 4, Issue , 2013, Pages

Cadmium iodide-mediated allenylation of terminal alkynes with ketones

Author keywords

[No Author keywords available]

Indexed keywords

1,5 BISALLENE DERIVATIVE; ALKYNE; ALLENE DERIVATIVE; CADMIUM; CADMIUM IODIDE; KETONE; UNCLASSIFIED DRUG;

EID: 84904558670     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms3450     Document Type: Article
Times cited : (59)

References (54)
  • 1
    • 4544276732 scopus 로고    scopus 로고
    • Synthesis and properties of allenic natural products and pharmaceuticals
    • Hoffmann-Röder, A. & Krause, N. Synthesis and properties of allenic natural products and pharmaceuticals. Angew. Chem. Int. Ed. 43, 1196-1216 (2004).
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 1196-1216
    • Hoffmann-Röder, A.1    Krause, N.2
  • 2
    • 33746940317 scopus 로고    scopus 로고
    • Structures and absolute stereochemistry of nipponallene and neonipponallene, new brominated allenes from the red alga Laurencia nipponica
    • Lyakhova, E. G. et al. Structures and absolute stereochemistry of nipponallene and neonipponallene, new brominated allenes from the red alga Laurencia nipponica. Tetrahedron Lett. 47, 6549-6552 (2006).
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6549-6552
    • Lyakhova, E.G.1
  • 3
    • 61349137576 scopus 로고    scopus 로고
    • The brosimum allene: A structural revision
    • Hu, G., Liu, K. & Williams, L. J. The brosimum allene: a structural revision. Org. Lett. 10, 5493-5496 (2008).
    • (2008) Org. Lett. , vol.10 , pp. 5493-5496
    • Hu, G.1    Liu, K.2    Williams, L.J.3
  • 4
    • 84870862154 scopus 로고    scopus 로고
    • Concise substrate-controlled asymmetric total syntheses of dioxabicyclic marine natural products with 2,10-dioxabicyclo-[7.3.0]dodecene and 2,9-dioxabicyclo[6.3.0]undecene skeletons
    • Kim, M. J., Sohn, T., Kim, D. & Paton, R. S. Concise substrate-controlled asymmetric total syntheses of dioxabicyclic marine natural products with 2,10-dioxabicyclo-[7.3.0]dodecene and 2,9-dioxabicyclo[6.3.0]undecene skeletons. J. Am. Chem. Soc. 134, 20178-20188 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20178-20188
    • Kim, M.J.1    Sohn, T.2    Kim, D.3    Paton, R.S.4
  • 5
    • 0141765945 scopus 로고    scopus 로고
    • Transition metal-catalyzed/mediated reaction of allenes with a nucleophilic functionality connected to the α-carbon atom
    • Ma, S. Transition metal-catalyzed/mediated reaction of allenes with a nucleophilic functionality connected to the α-carbon atom. Acc. Chem. Res. 36, 701-712 (2003).
    • (2003) Acc. Chem. Res. , vol.36 , pp. 701-712
    • Ma, S.1
  • 6
    • 22944485617 scopus 로고    scopus 로고
    • Some typical advances in the synthetic applications of allenes
    • Ma, S. Some typical advances in the synthetic applications of allenes. Chem. Rev. 105, 2829-2871 (2005).
    • (2005) Chem. Rev. , vol.105 , pp. 2829-2871
    • Ma, S.1
  • 7
    • 38749110788 scopus 로고    scopus 로고
    • Recent advances in the chemistry of allenes
    • Ma, S. Recent advances in the chemistry of allenes. Aldrichimica Acta 40, 91-102 (2007).
    • (2007) Aldrichimica Acta , vol.40 , pp. 91-102
    • Ma, S.1
  • 8
    • 70350323591 scopus 로고    scopus 로고
    • Electrophilic addition and cyclization reactions of allenes
    • Ma, S. Electrophilic addition and cyclization reactions of allenes. Acc. Chem. Res. 42, 1679-1688 (2009).
    • (2009) Acc. Chem. Res. , vol.42 , pp. 1679-1688
    • Ma, S.1
  • 9
    • 84858780394 scopus 로고    scopus 로고
    • Allenes in catalytic asymmetric synthesis and natural product syntheses
    • Yu, S. & Ma, S. Allenes in catalytic asymmetric synthesis and natural product syntheses. Angew. Chem. Int. Ed. 51, 3074-3112 (2012).
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 3074-3112
    • Yu, S.1    Ma, S.2
  • 10
    • 4544245050 scopus 로고    scopus 로고
    • Pd-catalyzed coupling reactions involving propargylic/allenylic species
    • Ma, S. Pd-catalyzed coupling reactions involving propargylic/allenylic species. Eur. J. Org. Chem. 1175-1183 (2004).
    • (2004) Eur. J. Org. Chem. , pp. 1175-1183
    • Ma, S.1
  • 11
    • 0000770422 scopus 로고    scopus 로고
    • Cascade radical cyclizations via biradicals generated from enediynes, enyne-Allenes, and enyne-ketenes
    • Wang, K. K. Cascade radical cyclizations via biradicals generated from enediynes, enyne-Allenes, and enyne-ketenes. Chem. Rev. 96, 207-222 (1996).
    • (1996) Chem. Rev. , vol.96 , pp. 207-222
    • Wang, K.K.1
  • 12
    • 0034245863 scopus 로고    scopus 로고
    • Palladium-catalyzed reactions of allenes
    • Zimmer, R., Dinesh, C. U., Nandanan, E. & Khan, F. A. Palladium-catalyzed reactions of allenes. Chem. Rev. 100, 3067-3125 (2000).
    • (2000) Chem. Rev. , vol.100 , pp. 3067-3125
    • Zimmer, R.1    Dinesh, C.U.2    Nandanan, E.3    Khan, F.A.4
  • 13
    • 0034675566 scopus 로고    scopus 로고
    • New and selective metal catalyzed reactions of allenes
    • Hashmi, A. S. K. New and selective metal catalyzed reactions of allenes. Angrew. Chem. Int. Ed. 39, 3590-3593 (2000).
    • (2000) Angrew. Chem. Int. Ed , vol.39 , pp. 3590-3593
    • Hashmi, A.S.K.1
  • 14
    • 0038301132 scopus 로고    scopus 로고
    • Allenes from cyclopropanes and their use in organic synthesis-recent developments
    • Sydnes, L. K. Allenes from cyclopropanes and their use in organic synthesis-recent developments. Chem. Rev. 103, 1133-1150 (2003).
    • (2003) Chem. Rev. , vol.103 , pp. 1133-1150
    • Sydnes, L.K.1
  • 15
    • 0037395377 scopus 로고    scopus 로고
    • Cationic cyclopentannelation of allene ethers
    • Tius, M. A. Cationic cyclopentannelation of allene ethers. Acc. Chem. Res. 36, 284-290 (2003).
    • (2003) Acc. Chem. Res. , vol.36 , pp. 284-290
    • Tius, M.A.1
  • 16
    • 0142213273 scopus 로고    scopus 로고
    • The emergence of allenamides in organic synthesis
    • Wei, L.-L., Xiong, H. & Hsung, R. P. The emergence of allenamides in organic synthesis. Acc. Chem. Res. 36, 773-782 (2003).
    • (2003) Acc. Chem. Res. , vol.36 , pp. 773-782
    • Wei, L.-L.1    Xiong, H.2    Hsung, R.P.3
  • 17
    • 1942456717 scopus 로고    scopus 로고
    • Allenic compounds and isothiocyanates as key building units in the synthesis of heterocycles
    • Brandsma, L. & Nedolya, N. A. Allenic compounds and isothiocyanates as key building units in the synthesis of heterocycles. Synthesis 735-745 (2004).
    • (2004) Synthesis , pp. 735-745
    • Brandsma, L.1    Nedolya, N.A.2
  • 18
    • 61849124839 scopus 로고    scopus 로고
    • Sugars, alkaloids, and heteroaromatics: Exploring heterocyclic chemistry with alkoxyallenes
    • Brasholz, M., Reissig, H.-U. & Zimmer, R. Sugars, alkaloids, and heteroaromatics: exploring heterocyclic chemistry with alkoxyallenes. Acc. Chem. Res. 42, 45-56 (2009).
    • (2009) Acc. Chem. Res. , vol.42 , pp. 45-56
    • Brasholz, M.1    Reissig, H.-U.2    Zimmer, R.3
  • 19
    • 0023837402 scopus 로고
    • Synthesis of the bicyclic core of the esperamicin/calichemicin class of antitumor agents
    • Schreiber, S. L. & Kiessling, L. L. Synthesis of the bicyclic core of the esperamicin/calichemicin class of antitumor agents. J. Am. Chem. Soc. 110, 631-633 (1988).
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 631-633
    • Schreiber, S.L.1    Kiessling, L.L.2
  • 20
    • 24144468234 scopus 로고    scopus 로고
    • What can a metal catalyst do with allenes? One-step formation of steroid scaffolds from readily available starting materials
    • Ma, S. et al. What can a metal catalyst do with allenes? One-step formation of steroid scaffolds from readily available starting materials. Angew. Chem. Int. Ed. 44, 5275-5278 (2005).
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 5275-5278
    • Ma, S.1
  • 21
    • 70349859708 scopus 로고    scopus 로고
    • Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A
    • Ghosh, P., Zhang, Y., Emge, T. J. & Williams, L. J. Modeling a macrocyclic bis[spirodiepoxide] strategy to erythronolide A. Org. Lett. 11, 4402-4405 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 4402-4405
    • Ghosh, P.1    Zhang, Y.2    Emge, T.J.3    Williams, L.J.4
  • 22
    • 74949137044 scopus 로고    scopus 로고
    • A concise synthesis of (-)- and (+)-trans-whisky lactones
    • Jiang, X., Fu, C. & Ma, S. A concise synthesis of (-)- and (+)-trans-whisky lactones. Eur. J. Org. Chem. 687-693 (2009).
    • (2009) Eur. J. Org. Chem. , pp. 687-693
    • Jiang, X.1    Fu, C.2    Ma, S.3
  • 23
    • 81255166935 scopus 로고    scopus 로고
    • General Au-catalyzed benzannulation towards naturally occurring carbazole alkaloids from methoxypropadiene
    • Kong, W., Fu, C. & Ma, S. General Au-catalyzed benzannulation towards naturally occurring carbazole alkaloids from methoxypropadiene. Chem. Eur. J. 17, 13134-13137 (2011).
    • (2011) Chem. Eur. J , vol.17 , pp. 13134-13137
    • Kong, W.1    Fu, C.2    Ma, S.3
  • 24
    • 84862195347 scopus 로고    scopus 로고
    • Highly selective mild stepwise allylation of N-methoxybenzamides with allenes
    • Zeng, R., Fu, C. & Ma, S. Highly selective mild stepwise allylation of N-methoxybenzamides with allenes. J. Am. Chem. Soc. 134, 9597-9600 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9597-9600
    • Zeng, R.1    Fu, C.2    Ma, S.3
  • 25
    • 84864407860 scopus 로고    scopus 로고
    • One-pot approach to installing eight-membered rings onto indoles
    • Zhu, C., Zhang, X., Lian, X. & Ma, S. One-pot approach to installing eight-membered rings onto indoles. Angew. Chem. Int. Ed. 51, 7817-7820 (2012).
    • (2012) Angew. Chem. Int. Ed , vol.51 , pp. 7817-7820
    • Zhu, C.1    Zhang, X.2    Lian, X.3    Ma, S.4
  • 26
    • 8444234639 scopus 로고    scopus 로고
    • Synthesis of allenes with organometallic reagents
    • Krause, N. & Hoffmann-Röder, A. Synthesis of allenes with organometallic reagents. Tetrahedron 60, 11671-11694 (2004).
    • (2004) Tetrahedron , vol.60 , pp. 11671-11694
    • Krause, N.1    Hoffmann-Röder, A.2
  • 27
    • 33947667037 scopus 로고    scopus 로고
    • Synthesizing allenes today (1982-2006)
    • Brummond, K. M. & DeForrest, J. E. Synthesizing allenes today (1982-2006). Synthesis 795-818 (2007).
    • (2007) Synthesis , pp. 795-818
    • Brummond, K.M.1    DeForrest, J.E.2
  • 28
    • 62849093017 scopus 로고    scopus 로고
    • Catalytic enantioselective synthesis of axially chiral allenes
    • Ogasawara, M. Catalytic enantioselective synthesis of axially chiral allenes. Tetrahedron: Asymmetry 20, 259-271 (2009).
    • (2009) Tetrahedron: Asymmetry , vol.20 , pp. 259-271
    • Ogasawara, M.1
  • 29
    • 79955164155 scopus 로고    scopus 로고
    • How easy are the syntheses of allenes?
    • Yu, S. & Ma, S. How easy are the syntheses of allenes? Chem. Commun. 47, 5384-5418 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 5384-5418
    • Yu, S.1    Ma, S.2
  • 30
    • 0344012926 scopus 로고    scopus 로고
    • Iron-catalyzed cross-coupling reactions: Efficient synthesis of 2,3-allenol derivatives
    • Fürstner, A. & Méndez, M. Iron-catalyzed cross-coupling reactions: efficient synthesis of 2,3-allenol derivatives. Angew. Chem. Int. Ed. 42, 5355-5357 (2003).
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 5355-5357
    • Fürstner, A.1    Méndez, M.2
  • 31
    • 2442419095 scopus 로고    scopus 로고
    • Synthesis of allenes via palladium-catalyzed hydrogen-transfer reactions: Propargylic amines as an allenyl anion equivalent
    • Nakamura, H., Kamakura, T., Ishikura, M. & Biellmann, J.-F. Synthesis of allenes via palladium-catalyzed hydrogen-transfer reactions: propargylic amines as an allenyl anion equivalent. J. Am. Chem. Soc. 126, 5958-5959 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5958-5959
    • Nakamura, H.1    Kamakura, T.2    Ishikura, M.3    Biellmann, J.-F.4
  • 32
    • 34248146411 scopus 로고    scopus 로고
    • Small but effective: Copper hydride catalyzed synthesis of α-hydroxyallenes
    • Deutsch, C., Lipshutz, B. H. & Krause, N. Small but effective: copper hydride catalyzed synthesis of α-hydroxyallenes. Angew. Chem. Int. Ed. 46, 1650-1653 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1650-1653
    • Deutsch, C.1    Lipshutz, B.H.2    Krause, N.3
  • 34
    • 67650517372 scopus 로고    scopus 로고
    • Enantioselective synthesis of chiral allenoates by Guanidine-catalyzed isomerization of 3-alkynoates
    • Liu, H., Leow, D., Huang, K.-W. & Tan, C.-H. Enantioselective synthesis of chiral allenoates by Guanidine-catalyzed isomerization of 3-alkynoates. J. Am. Chem. Soc. 131, 7212-7213 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 7212-7213
    • Liu, H.1    Leow, D.2    Huang, K.-W.3    Tan, C.-H.4
  • 35
    • 70349124215 scopus 로고    scopus 로고
    • Allene synthesis via C-C fragmentation: Method and mechanistic insight
    • Kolakowski, R. V., Manpadi, M., Zhang, Y., Emge, T. J. & Williams, L. J. Allene synthesis via C-C fragmentation: method and mechanistic insight. J. Am. Chem. Soc. 131, 12910-12911 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 12910-12911
    • Kolakowski, R.V.1    Manpadi, M.2    Zhang, Y.3    Emge, T.J.4    Williams, L.J.5
  • 36
    • 77952863831 scopus 로고    scopus 로고
    • Gold(I)-catalyzed rearrangement of propargyl benzyl ethers: A practical method for the generation and in situ transformation of substituted allenes
    • Bolte, B., Odabachian, Y. & Gagosz, F. Gold(I)-catalyzed rearrangement of propargyl benzyl ethers: a practical method for the generation and in situ transformation of substituted allenes. J. Am. Chem. Soc. 132, 7294-7296 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 7294-7296
    • Bolte, B.1    Odabachian, Y.2    Gagosz, F.3
  • 38
    • 0000153311 scopus 로고
    • One-step homologation of acetylenes to allenes: 4-hydroxynona-1,2-diene
    • Crabbé, P., Nassim, B. & Robert-Lopes, M.-T. One-step homologation of acetylenes to allenes: 4-hydroxynona-1,2-diene. Org. Synth. 63, 203-204 (1985).
    • (1985) Org. Synth. , vol.63 , pp. 203-204
    • Crabbé, P.1    Nassim, B.2    Robert-Lopes, M.-T.3
  • 39
    • 64349105023 scopus 로고    scopus 로고
    • An efficient synthesis of terminal allenes from terminal 1-alkynes
    • Kuang, J. & Ma, S. An efficient synthesis of terminal allenes from terminal 1-alkynes. J. Org. Chem. 74, 1763-1765 (2009).
    • (2009) J. Org. Chem. , vol.74 , pp. 1763-1765
    • Kuang, J.1    Ma, S.2
  • 40
    • 84877747927 scopus 로고    scopus 로고
    • CuI-catalyzed synthesis of functionalized terminal allenes from 1-alkynes
    • Luo, H. & Ma, S. CuI-catalyzed synthesis of functionalized terminal allenes from 1-alkynes. Eur. J. Org. Chem. 3041-3048 (2013).
    • (2013) Eur. J. Org. Chem. , pp. 3041-3048
    • Luo, H.1    Ma, S.2
  • 41
    • 77249148886 scopus 로고    scopus 로고
    • One-pot synthesis of 1,3-disubstituted allenes from 1-alkynes, aldehydes, and morpholine
    • Kuang, J. & Ma, S. One-pot synthesis of 1,3-disubstituted allenes from 1-alkynes, aldehydes, and morpholine. J. Am. Chem. Soc. 132, 1786-1787 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1786-1787
    • Kuang, J.1    Ma, S.2
  • 42
    • 35348920555 scopus 로고    scopus 로고
    • Allene formation by gold catalyzed cross-coupling of masked carbenes and vinylidenes
    • Lavallo, V., Frey, G. D., Kousar, S., Donnadieu, B. & Bertrand, G. Allene formation by gold catalyzed cross-coupling of masked carbenes and vinylidenes. Proc. Natl Acad. Sci. USA 104, 13569-13573 (2007).
    • (2007) Proc. Natl Acad. Sci. USA , vol.104 , pp. 13569-13573
    • Lavallo, V.1    Frey, G.D.2    Kousar, S.3    Donnadieu, B.4    Bertrand, G.5
  • 43
    • 79251568604 scopus 로고    scopus 로고
    • Coupling of N-tosylhydrazones with terminal alkynes catalyzed by copper(I): Synthesis of trisubstituted allenes
    • Xiao, Q., Xia, Y., Li, H., Zhang, Y. & Wang, J. Coupling of N-tosylhydrazones with terminal alkynes catalyzed by copper(I): synthesis of trisubstituted allenes. Angew. Chem. Int. Ed. 50, 1114-1117 (2011).
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 1114-1117
    • Xiao, Q.1    Xia, Y.2    Li, H.3    Zhang, Y.4    Wang, J.5
  • 44
    • 79651474664 scopus 로고    scopus 로고
    • Highly efficient cadmium-catalyzed three-component coupling of an aldehyde, alkyne, and amine via C-H activation under microwave conditions
    • Raghuvanshi, D. S. & Singh, K. N. Highly efficient cadmium-catalyzed three-component coupling of an aldehyde, alkyne, and amine via C-H activation under microwave conditions. Synlett. 3, 373-377 (2011).
    • (2011) Synlett , vol.3 , pp. 373-377
    • Raghuvanshi, D.S.1    Singh, K.N.2
  • 45
    • 0034805417 scopus 로고    scopus 로고
    • Chemoselective dithioacetalisation of carbonyl compounds under solvent-free conditions
    • Laskar, D. D., Prajapati, D. & Sandhu, J. S. Chemoselective dithioacetalisation of carbonyl compounds under solvent-free conditions. J. Chem. Research (S) 313-315 (2001).
    • (2001) J. Chem. Research (S) , pp. 313-315
    • Laskar, D.D.1    Prajapati, D.2    Sandhu, J.S.3
  • 46
    • 84858760279 scopus 로고    scopus 로고
    • Copper (I) iodide-catalyzed one-step preparation of functionalized allenes from terminal alkynes: Amine effect
    • Kuang, J., Luo, H. & Ma, S. Copper (I) iodide-catalyzed one-step preparation of functionalized allenes from terminal alkynes: amine effect. Adv. Synth. Catal. 354, 933-944 (2012).
    • (2012) Adv. Synth. Catal , vol.354 , pp. 933-944
    • Kuang, J.1    Luo, H.2    Ma, S.3
  • 47
    • 75649145831 scopus 로고    scopus 로고
    • Silver(I)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions
    • Lo, V. K.-Y., Zhou, C.-Y., Wong, M.-K. & Che, C.-M. Silver(I)-mediated highly enantioselective synthesis of axially chiral allenes under thermal and microwave-assisted conditions. Chem. Commun. 46, 213-215 (2010).
    • (2010) Chem. Commun. , vol.46 , pp. 213-215
    • Lo, V.K.-Y.1    Zhou, C.-Y.2    Wong, M.-K.3    Che, C.-M.4
  • 48
    • 38949112395 scopus 로고    scopus 로고
    • Gold-catalyzed highly enantioselective synthesis of axially chiral allenes
    • Lo, V. K.-Y., Zhou, C.-Y. & Che, C.-M. Gold-catalyzed highly enantioselective synthesis of axially chiral allenes. Org. Lett. 10, 517-519 (2008).
    • (2008) Org. Lett. , vol.10 , pp. 517-519
    • Lo, V.K.-Y.1    Zhou, C.-Y.2    Che, C.-M.3
  • 49
    • 35048860971 scopus 로고    scopus 로고
    • 2-catalyzed monomeric and dimeric cycloisomerization of propargylic 2,3-dienoates. Establishment of α,β-unsaturated δ-lactone rings by cyclometallation
    • 2-catalyzed monomeric and dimeric cycloisomerization of propargylic 2,3-dienoates. establishment of α,β-unsaturated δ-lactone rings by cyclometallation. J. Am. Chem. Soc. 129, 11600-11607 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 11600-11607
    • Jiang, X.1    Ma, S.2
  • 50
    • 0001613006 scopus 로고    scopus 로고
    • Ruthenium-catalyzed cyclic carbonylation of allenyl alcohols. Selective synthesis of γ- and δ-lactones
    • Yoneda, E., Kaneko, T., Zhang, S.-W., Onitsuka, K. & Takahashi, S. Ruthenium-catalyzed cyclic carbonylation of allenyl alcohols. selective synthesis of γ- and δ-lactones. Org. Lett. 2, 441-443 (2000).
    • (2000) Org. Lett. , vol.2 , pp. 441-443
    • Yoneda, E.1    Kaneko, T.2    Zhang, S.-W.3    Onitsuka, K.4    Takahashi, S.5
  • 51
    • 53149126046 scopus 로고    scopus 로고
    • Two-step allylic carbon insertion between ketone carbonyl and α carbons giving a-quaternary α-vinyl ketones
    • He, J.-Q., Shibata, D., Ohno, C. & Okamoto, S. Two-step allylic carbon insertion between ketone carbonyl and α carbons giving a-quaternary α-vinyl ketones. Tetrahedron Lett. 49, 6724-6727 (2008).
    • (2008) Tetrahedron Lett. , vol.49 , pp. 6724-6727
    • He, J.-Q.1    Shibata, D.2    Ohno, C.3    Okamoto, S.4
  • 52
    • 84870039306 scopus 로고    scopus 로고
    • 3-catalyzed cyclization of α-sulfonamido-allenes with aldehydes - The substituent effect
    • 3-catalyzed cyclization of α-sulfonamido-allenes with aldehydes - the substituent effect. Chem. Commun. 48, 12074-12076 (2012).
    • (2012) Chem. Commun. , vol.48 , pp. 12074-12076
    • Cheng, J.1    Tang, X.2    Yu, Y.3    Ma, S.4
  • 53
    • 84875948368 scopus 로고    scopus 로고
    • 3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes
    • 3-Catalyzed Cyclization of β-Sulfonamidoallenes or β-Allenols and Aldehydes. ACS Catal. 3, 663-666 (2013).
    • (2013) ACS Catal , vol.3 , pp. 663-666
    • Cheng, J.1    Tang, X.2    Ma, S.3
  • 54
    • 84862213126 scopus 로고    scopus 로고
    • Gold-catalyzed isomerization of unactivated allenes into 1,3-dienes under ambient conditions
    • Ting, C.-M., Hsu, Y.-L. & Liu, R.-S. Gold-catalyzed isomerization of unactivated allenes into 1,3-dienes under ambient conditions. Chem. Commun. 48, 6577-6579 (2012).
    • (2012) Chem. Commun. , vol.48 , pp. 6577-6579
    • Ting, C.-M.1    Hsu, Y.-L.2    Liu, R.-S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.