메뉴 건너뛰기




Volumn 15, Issue 10, 2011, Pages 1625-1643

The construction of five-membered heterocycles by transition metal-catalyzed cyclization of propargylic compounds

Author keywords

Cascade reaction; Cyclization; Heterocycle; Propargylic compound; Transition metal

Indexed keywords

ADDITION REACTIONS; CATALYSIS; CATALYST ACTIVITY; CHEMICAL BONDS; CYCLIZATION; METAL COMPLEXES; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL); THIOPHENE; TRANSITION METAL COMPOUNDS;

EID: 79955044505     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527211795378100     Document Type: Article
Times cited : (20)

References (100)
  • 1
    • 51049114031 scopus 로고    scopus 로고
    • Coinage metal-assisted synthesis of heterocycles
    • Patil, N. T.; Yamamoto, Y. Coinage metal-assisted synthesis of heterocycles. Chem. Rev. 2008, 108, 3395-3442;
    • (2008) Chem. Rev , vol.108 , pp. 3395-3442
    • Patil, N.T.1    Yamamoto, Y.2
  • 2
    • 58449124067 scopus 로고    scopus 로고
    • Metal-catalyzed one-step synthesis: Towards direct alternatives to multistep heterocycle and amino acid derivative formation
    • Arndtsen, B.A. Metal-catalyzed one-step synthesis: towards direct alternatives to multistep heterocycle and amino acid derivative formation. Chem. Eur. J. 2009, 15, 302-313;
    • (2009) Chem. Eur. J , vol.15 , pp. 302-313
    • Arndtsen, B.A.1
  • 3
    • 4444376920 scopus 로고    scopus 로고
    • Transition-metal-catalyzed addition of heteroatom-hydrogen bonds to alkynes
    • Alonso, F.; Beletskaya, I. P.; Yus, M. Transition-metal-catalyzed addition of heteroatom-hydrogen bonds to alkynes. Chem. Rev. 2004, 104, 3079-3159;
    • (2004) Chem. Rev , vol.104 , pp. 3079-3159
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 4
    • 53849089263 scopus 로고    scopus 로고
    • 1, 2-Alkyl migration as a key element in the invention of cascade reactions catalyzed by Ji-acids
    • Crone, B.; Kirsch, S. F. 1, 2-Alkyl migration as a key element in the invention of cascade reactions catalyzed by Ji-acids. Chem. Eur. J. 2008, 14, 3514-3522;
    • (2008) Chem. Eur. J , vol.14 , pp. 3514-3522
    • Crone, B.1    Kirsch, S.F.2
  • 5
    • 33744802336 scopus 로고    scopus 로고
    • Syntheses of poly substituted furans: Recent developments
    • Kirsch, S. F. Syntheses of poly substituted furans: recent developments. Org. Biomol. Chem. 2006, 4, 2076-2080;
    • (2006) Org. Biomol. Chem , vol.4 , pp. 2076-2080
    • Kirsch, S.F.1
  • 6
    • 34047228439 scopus 로고    scopus 로고
    • Recent developments in the metal-catalyzed reactions of metallocarbenoids from propargylic esters
    • Contelles, J. M.; Sorian, E. Recent developments in the metal-catalyzed reactions of metallocarbenoids from propargylic esters. Chem. Eur. J. 2007, 13, 1350-1357;
    • (2007) Chem. Eur. J , vol.13 , pp. 1350-1357
    • Contelles, J.M.1    Sorian, E.2
  • 7
    • 2942557280 scopus 로고    scopus 로고
    • Transition-Metal-catalyzed reactions in heterocyclic synthesis
    • Nakamura I.; Yamamoto, Y. Transition-Metal-catalyzed reactions in heterocyclic synthesis. Chem. Rev. 2004, 104, 2127-2198;
    • (2004) Chem. Rev , vol.104 , pp. 2127-2198
    • Nakamura, I.1    Yamamoto, Y.2
  • 8
    • 51049094897 scopus 로고    scopus 로고
    • Cu-catalyzed azide-alkyne cycloaddition
    • Meldal, M.; Tornøe, C. W. Cu-catalyzed azide-alkyne cycloaddition. Chem. Rev. 2008,108, 2952-3015.
    • (2008) Chem. Rev , vol.108 , pp. 2952-3015
    • Meldal, M.1    Tornøe, C.W.2
  • 9
    • 51049115331 scopus 로고    scopus 로고
    • Asymmetric silver-catalyzed reactions
    • Naodovic, M.; Yamamoto, H. Asymmetric silver-catalyzed reactions. Chem. Rev. 2008, 108, 3132-3148;
    • (2008) Chem. Rev , vol.108 , pp. 3132-3148
    • Naodovic, M.1    Yamamoto, H.2
  • 10
    • 51049094424 scopus 로고    scopus 로고
    • Enantioselective Copper-Catalyzed 1, 3-Dipolar Cycloadditions
    • Stanley, S.M.; Sibi, M.P. Enantioselective Copper-Catalyzed 1, 3-Dipolar Cycloadditions. Chem. Rev. 2008,108, 2887-2902.
    • (2008) Chem. Rev , vol.108 , pp. 2887-2902
    • Stanley, S.M.1    Sibi, M.P.2
  • 11
    • 51049121927 scopus 로고    scopus 로고
    • Gold-catalyzed organic transformations
    • Li, Z.; Brouwer, C; He, C. Gold-catalyzed organic transformations. Chem. Rev. 2008, 108, 3239-3265;
    • (2008) Chem. Rev , vol.108 , pp. 3239-3265
    • Li, Z.1    Brouwer, C.2    He, C.3
  • 12
    • 51249100498 scopus 로고    scopus 로고
    • Alternative synthetic methods through new developments in catalysis by gold
    • Arcadi, A. Alternative synthetic methods through new developments in catalysis by gold. Chem. Rev. 2008,108, 3266-3325;
    • (2008) Chem. Rev , vol.108 , pp. 3266-3325
    • Arcadi, A.1
  • 13
    • 34547510627 scopus 로고    scopus 로고
    • Gold-catalyzed organic reactions
    • Hashmi, A. S. K. Gold-catalyzed organic reactions. Chem. Rev. 2007,107, 3180-3211;
    • (2007) Chem. Rev , vol.107 , pp. 3180-3211
    • Hashmi, A.S.K.1
  • 15
    • 0141615958 scopus 로고    scopus 로고
    • Gold-catalyzed hydroarylation of alkynes
    • Reetz, M. T.; Sommer, K. Gold-catalyzed hydroarylation of alkynes. Eur. J. Org. Chem. 2003, 3485-3496.
    • (2003) Eur. J. Org. Chem , pp. 3485-3496
    • Reetz, M.T.1    Sommer, K.2
  • 16
    • 40949091926 scopus 로고    scopus 로고
    • Recent advances in syntheses of heterocycles and carbocycles via homogeneous gold catalysis. part 1: Heteroatom addition and hydroarylation reactions of alkynes, allenes, and alkenes
    • Shen, H. C. Recent advances in syntheses of heterocycles and carbocycles via homogeneous gold catalysis. part 1: heteroatom addition and hydroarylation reactions of alkynes, allenes, and alkenes. Tetrahedron, 2008, 64, 3885-3903.
    • (2008) Tetrahedron , vol.64 , pp. 3885-3903
    • Shen, H.C.1
  • 17
    • 33947578482 scopus 로고    scopus 로고
    • Relativistic effects in homogeneous gold catalysis
    • Gorin, D. G.; Toste, F. D. Relativistic effects in homogeneous gold catalysis. Nature, 2007, 446, 395-403.
    • (2007) Nature , vol.446 , pp. 395-403
    • Gorin, D.G.1    Toste, F.D.2
  • 18
    • 0037463685 scopus 로고    scopus 로고
    • Stability of the gold(i)-phosphine bond. a comparison with other group 11 elements
    • Schwerdtfeger, P., Hermann, H. L.; Schmidbaur, H. Stability of the gold(i)-phosphine bond. a comparison with other group 11 elements. Inorg. Chem. 2003,42, 1334-1342.
    • (2003) Inorg. Chem , vol.42 , pp. 1334-1342
    • Schwerdtfeger, P.1    Hermann, H.L.2    Schmidbaur, H.3
  • 19
    • 37049155415 scopus 로고
    • Olefin Co-ordination compounds. Part III. Infra-red Spectra and Structure: Attempted Preparation of Acetylene Complexes
    • Chatt, J.; Duncanson, L. A. Olefin Co-ordination compounds. Part III. Infra-red Spectra and Structure: Attempted Preparation of Acetylene Complexes. J. Chem. Soc. 1953, 2939-2947.
    • (1953) J. Chem. Soc , pp. 2939-2947
    • Chatt, J.1    Duncanson, L.A.2
  • 20
    • 37049064829 scopus 로고
    • Directing Effects in inorganic substitution reactions. part i. a hypothesis to explain the trans-effect
    • Chatt, J.; Duncanson, L. A.; Venanzi, L. M. Directing Effects in inorganic substitution reactions. part i. a hypothesis to explain the trans-effect. J. Chem. Soc. 1955, 4456-4460.
    • (1955) J. Chem. Soc , pp. 4456-4460
    • Chatt, J.1    Duncanson, L.A.2    Venanzi, L.M.3
  • 21
    • 51049105959 scopus 로고    scopus 로고
    • Ligand effects in homogeneous au catalysis
    • Gorin, D. J.; Sherry, B. D.; Toste, F. D. Ligand effects in homogeneous au catalysis. Chem. Rev. 2008,108, 3351-3378.
    • (2008) Chem. Rev , vol.108 , pp. 3351-3378
    • Gorin, D.J.1    Sherry, B.D.2    Toste, F.D.3
  • 22
    • 33747272412 scopus 로고    scopus 로고
    • Gold-catalyzed highly efficient access to 3(2h)-furanones from 2-oxo-3-butynoates and related compounds
    • Liu, Y.; Liu, M.; Guo, S.; Tu, H.; Zhou, Y.; Gao, H. Gold-catalyzed highly efficient access to 3(2h)-furanones from 2-oxo-3-butynoates and related compounds. Org. Lett. 2006, 8, 3445-3448.
    • (2006) Org. Lett , vol.8 , pp. 3445-3448
    • Liu, Y.1    Liu, M.2    Guo, S.3    Tu, H.4    Zhou, Y.5    Gao, H.6
  • 23
    • 9444284312 scopus 로고    scopus 로고
    • Gold catalysis: Mild conditions for the synthesis of oxazoles from n-propargylcarboxamides and mechanistic aspects
    • Hashmi, A. S. K.; Weyrauch, J. P.; Frey, W.; Bats, J. W. Gold catalysis: mild conditions for the synthesis of oxazoles from n-propargylcarboxamides and mechanistic aspects. Org. Lett. 2004, 6, 4391-4394.
    • (2004) Org. Lett , vol.6 , pp. 4391-4394
    • Hashmi, A.S.K.1    Weyrauch, J.P.2    Frey, W.3    Bats, J.W.4
  • 24
    • 34547870137 scopus 로고    scopus 로고
    • Mechanistically diverse copper-, silver-, and gold-catalyzed acyloxy and phosphatyloxy migrations: Efficient synthesis of heterocycles via cascade migration/cycloisomerization approach
    • Schwier, T.; Sromek, A. W.; Yap, D. M. L.; Chernyak, D.; Gevorgyan, V. Mechanistically diverse copper-, silver-, and gold-catalyzed acyloxy and phosphatyloxy migrations: efficient synthesis of heterocycles via cascade migration/cycloisomerization approach. J. Am. Chem. Soc. 2007, 129, 9868-9878.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 9868-9878
    • Schwier, T.1    Sromek, A.W.2    Yap, D.M.L.3    Chernyak, D.4    Gevorgyan, V.5
  • 28
    • 4544255270 scopus 로고    scopus 로고
    • 3-catalyzed synthesis of highly substituted furans from 2-(1-alkynyl)-2-alken-1-ones
    • Yao, T.; Zhang, X.; Larock, R. C. AuCl3-catalyzed synthesis of highly substituted furans from 2-(1-alkynyl)-2-alken-1-ones. J. Am. Chem. Soc. 2004,126, 11164-11165.
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 11164-11165
    • Yao, T.1    Zhang, X.2    Larock, R.C.3
  • 29
    • 24944452788 scopus 로고    scopus 로고
    • Gold(I)-catalyzed synthesis of highly substituted furans
    • Suhre, M. H.; Reif, M.; Kirsch, S. F. Gold(I)-catalyzed synthesis of highly substituted furans. Org. Lett. 2005, 7, 3925-3927.
    • (2005) Org. Lett , vol.7 , pp. 3925-3927
    • Suhre, M.H.1    Reif, M.2    Kirsch, S.F.3
  • 30
    • 33744720086 scopus 로고    scopus 로고
    • Synthesis of highly substituted pyrroles via a multimetal-catalyzed. rearrangement-condensation-cyclization domino approach
    • Binder, J. T.; Kirsch, S. F. Synthesis of highly substituted pyrroles via a multimetal-catalyzed. rearrangement-condensation-cyclization domino approach. Org. Lett. 2006, 8, 2151-2153.
    • (2006) Org. Lett , vol.8 , pp. 2151-2153
    • Binder, J.T.1    Kirsch, S.F.2
  • 31
    • 33750347225 scopus 로고    scopus 로고
    • Synthesis of stable 2H-pyran-5-carboxylates via a catalyzed propargyl-claisen rearrangement/Oxa-6;r electrocyclization strategy
    • Menz, H.; Kirsch, S. F. Synthesis of stable 2H-pyran-5-carboxylates via a catalyzed propargyl-claisen rearrangement/Oxa-6;r electrocyclization strategy. Org. Lett. 2006, 8, 4795-4797.
    • (2006) Org. Lett , vol.8 , pp. 4795-4797
    • Menz, H.1    Kirsch, S.F.2
  • 32
    • 2342666651 scopus 로고    scopus 로고
    • Gold catalysis: Mild conditions for the transformation of alkynyl epoxides to furans
    • Hashmi, A. S. K.; Sinha, P. Gold catalysis: mild conditions for the transformation of alkynyl epoxides to furans. Adv. Synth. Catal. 2004, 346, 432-438.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 432-438
    • Hashmi, A.S.K.1    Sinha, P.2
  • 33
    • 36749091693 scopus 로고    scopus 로고
    • Gold-catalyzed tandem cycloisomerization of alkynyloxiranes with nucleophiles: An efficient approach to 2,5-disubstituted furans
    • Shu, X.; Liu, X.; Xiao, H.; Ji, K. Guo, L.; Qi, C; Liang, Y. Gold-catalyzed tandem cycloisomerization of alkynyloxiranes with nucleophiles: An efficient approach to 2,5-disubstituted furans. Adv. Synth. Catal. 2007, 349, 2493-2498.
    • (2007) Adv. Synth. Catal , vol.349 , pp. 2493-2498
    • Shu, X.1    Liu, X.2    Xiao, H.3    Ji, K.4    Guo, L.5    Qi, C.6    Liang, Y.7
  • 34
    • 68049099260 scopus 로고    scopus 로고
    • Mechanistic studies and improvement of coinage metal-catalyzed transformation of alkynyloxiranes to furans: An alcohol addition-cyclization-elimination cascade
    • Blanc, A.; Tenbrink, K.; Weibel, J.; Pale, P. Mechanistic studies and improvement of coinage metal-catalyzed transformation of alkynyloxiranes to furans: an alcohol addition-cyclization-elimination cascade. J. Org. Chem. 2009, 74, 5342-5348.
    • (2009) J. Org. Chem , vol.74 , pp. 5342-5348
    • Blanc, A.1    Tenbrink, K.2    Weibel, J.3    Pale, P.4
  • 35
    • 34447321835 scopus 로고    scopus 로고
    • Synthesis of 4-Iodo-3-furanones utilizing electrophile-induced tandem cyclization/1,2-migration reactions
    • Crone, B.; Kirsch, S. F. Synthesis of 4-Iodo-3-furanones utilizing electrophile-induced tandem cyclization/1,2-migration reactions. J. Org. Chem. 2007, 72, 5435-5438.
    • (2007) J. Org. Chem , vol.72 , pp. 5435-5438
    • Crone, B.1    Kirsch, S.F.2
  • 36
    • 23844478167 scopus 로고    scopus 로고
    • Gold(I)-Catalyzed intramolecular acetylenic schmidt reaction
    • Gorin, D. J.; Davis, N. R.; Toste, F. D. Gold(I)-Catalyzed intramolecular acetylenic schmidt reaction. J. Am. Chem. Soc. 2005, 127, 11260-11261.
    • (2005) J. Am. Chem. Soc , vol.1 , Issue.27 , pp. 11260-11261
    • Gorin, D.J.1    Davis, N.R.2    Toste, F.D.3
  • 37
    • 58549097865 scopus 로고    scopus 로고
    • An efficient domino approach for the synthesis of multisubstituted pyrroles via gold/silver-catalyzed amination/cycloisomerization of (z)-2-en-4-yn-1-ols
    • Lu, Y.; Fu, X.; Chen, H.; Du, X.; Jia, X.; Liu, Y. An efficient domino approach for the synthesis of multisubstituted pyrroles via gold/silver-catalyzed amination/cycloisomerization of (z)-2-en-4-yn-1-ols. Adv. Synth. Catal. 2009, 351, 129-134.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 129-134
    • Lu, Y.1    Fu, X.2    Chen, H.3    Du, X.4    Jia, X.5    Liu, Y.6
  • 38
    • 67650472201 scopus 로고    scopus 로고
    • Gold-catalyzed intermolecular reactions of (z)-enynols with indoles for the construction of dihydrocyclohepta[b]indole skeletons through a cascade friedel-crafts/hydroarylation sequence
    • Lu, Y.; Du, X.; Jia, X.; Liu, Y. Gold-catalyzed intermolecular reactions of (z)-enynols with indoles for the construction of dihydrocyclohepta[b]indole skeletons through a cascade friedel-crafts/hydroarylation sequence. Adv. Synth. Catal. 2009,351, 1517-1522.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 1517-1522
    • Lu, Y.1    Du, X.2    Jia, X.3    Liu, Y.4
  • 39
    • 34547950964 scopus 로고    scopus 로고
    • Synthesis of functionalized pyrroles via gold(i)-catalyzed aza-claisen-type rearrangement
    • Istrate, F. M.; Gagosz, F. Synthesis of functionalized pyrroles via gold(i)-catalyzed aza-claisen-type rearrangement. Org. Lett. 2007, 9, 3181-3184.
    • (2007) Org. Lett , vol.9 , pp. 3181-3184
    • Istrate, F.M.1    Gagosz, F.2
  • 40
    • 0037944068 scopus 로고    scopus 로고
    • Palladium-assisted routes to nucleosides
    • Agrofoglio, L. A.; Gillaizeau, I.; Saito, Y. Palladium-assisted routes to nucleosides. Chem. Rev. 2003, 103, 1875-1916;
    • (2003) Chem. Rev , vol.103 , pp. 1875-1916
    • Agrofoglio, L.A.1    Gillaizeau, I.2    Saito, Y.3
  • 41
    • 2942609168 scopus 로고    scopus 로고
    • Synthesis of heterocycles via palladium ^-olefin and ff-alkyne chemistry
    • Zeni, G.; Larock, R C. Synthesis of heterocycles via palladium ^-olefin and ff-alkyne chemistry. Chem. Rev. 2004, 104, 2285-2309;
    • (2004) Chem. Rev , vol.104 , pp. 2285-2309
    • Zeni, G.1    Larock, R.C.2
  • 42
    • 0037943974 scopus 로고    scopus 로고
    • Palladium-catalyzed alkynylation
    • Negishi, E.; Anastasia, L. Palladium-catalyzed alkynylation. Chem. Rev. 2003, 103, 1979-2017;
    • (2003) Chem. Rev , vol.103 , pp. 1979-2017
    • Negishi, E.1    Anastasia, L.2
  • 43
    • 4043123499 scopus 로고    scopus 로고
    • Enantioselective palladium-catalyzed transformations
    • Tietze, L. F.; Ila, H.; Bell, H. P. Enantioselective palladium-catalyzed transformations. Chem. Rev. 2004, 104, 3453-3516.
    • (2004) Chem. Rev , vol.104 , pp. 3453-3516
    • Tietze, L.F.1    Ila, H.2    Bell, H.P.3
  • 44
    • 33846893890 scopus 로고    scopus 로고
    • Carbon-Carbon coupling reactions catalyzed by heterogeneous palladium catalysts
    • Yin, L.; Liebscher, J. Carbon-Carbon coupling reactions catalyzed by heterogeneous palladium catalysts. Chem. Rev. 2007, 107, 133-173;
    • (2007) Chem. Rev , vol.107 , pp. 133-173
    • Yin, L.1    Liebscher, J.2
  • 45
    • 33751424969 scopus 로고    scopus 로고
    • Synthesis of heterocycles via palladium-catalyzed oxidative addition
    • Zeni, G.; Larock, R C. Synthesis of heterocycles via palladium-catalyzed oxidative addition. Chem. Rev. 2006, 106, 4644-4680;
    • (2006) Chem. Rev , vol.106 , pp. 4644-4680
    • Zeni, G.1    Larock, R.C.2
  • 46
    • 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. 2000, 100, 3067-3125;
    • (2000) Chem. Rev , vol.100 , pp. 3067-3125
    • Zimmer, R.1    Dinesh, C.U.2    Nandanan, E.3    Khan, F.A.4
  • 47
    • 0034249671 scopus 로고    scopus 로고
    • The heck reaction as a sharpening stone of palladium catalysis
    • Beletskaya, I. P.; Cheprakov, A. V. The heck reaction as a sharpening stone of palladium catalysis. Chem. Rev. 2000, 100, 3009-3066.
    • (2000) Chem. Rev , vol.100 , pp. 3009-3066
    • Beletskaya, I.P.1    Cheprakov, A.V.2
  • 48
    • 0003441482 scopus 로고    scopus 로고
    • wiley & sons: New York
    • st century; wiley & sons: New York, 2004.
    • (2004) st Century
    • Tsuji, J.1
  • 52
    • 45249089674 scopus 로고    scopus 로고
    • Highly regio- and stereoselective synthesis of indene and benzo[b]furan derivatives via a Pd-catalyzed carboannulation of propargyl carbonates with nucleophiles
    • Bi, H.; Guo, L.; Gou, F.; Duan, X.; Liu, X.; Liang, Y. Highly regio- and stereoselective synthesis of indene and benzo[b]furan derivatives via a Pd-catalyzed carboannulation of propargyl carbonates with nucleophiles. J. Org. Chem. 2008, 73, 713-4716.
    • (2008) J. Org. Chem , vol.73 , pp. 713-4716
    • Bi, H.1    Guo, L.2    Gou, F.3    Duan, X.4    Liu, X.5    Liang, Y.6
  • 53
    • 34848888306 scopus 로고    scopus 로고
    • Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction
    • Bi, H.; Liu, X.; Gou, F.; Guo, L.; Duan, X.; Shu, X.; Liang, Y. Highly regioselective synthesis of spirocyclic compounds by a palladium-catalyzed intermolecular tandem reaction. Angew. Chem. Int. Ed. 2007, 46, 7068-7071.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 7068-7071
    • Bi, H.1    Liu, X.2    Gou, F.3    Guo, L.4    Duan, X.5    Shu, X.6    Liang, Y.7
  • 54
    • 33751315002 scopus 로고    scopus 로고
    • A new consecutive three-component oxazole synthesis by an amidation/coupling/cycloisomerization (acci) sequence
    • Merkul, E.; and Muller, T. J. J. A new consecutive three-component oxazole synthesis by an amidation/coupling/cycloisomerization (acci) sequence. Chem. Commun. 2006,4817-4819.
    • (2006) Chem. Commun , pp. 4817-4819
    • Merkul, E.1    Muller, T.J.J.2
  • 55
    • 45249091683 scopus 로고    scopus 로고
    • Intramolecular Pd(II)-catalyzed cyclization of propargylamides: Straightforward synthesis of 5-oxazolecarbaldehydes
    • Beccalli, E. M.; Borsini, E.; Broggini, G.; Palmisano, G.; Sottocornola, S. Intramolecular Pd(II)-catalyzed cyclization of propargylamides: straightforward synthesis of 5-oxazolecarbaldehydes. J. Org. Chem. 2008, 73, 4746-4749.
    • (2008) J. Org. Chem , vol.73 , pp. 4746-4749
    • Beccalli, E.M.1    Borsini, E.2    Broggini, G.3    Palmisano, G.4    Sottocornola, S.5
  • 56
    • 0034616109 scopus 로고    scopus 로고
    • Synthesis of 3-trifluoroethylfurans by palladium-catalyzed cyclization-isomerization of (z)-2-alkynyl-3-trifluoromethyl allylic alcohols
    • Qing, F.; Gao, W.; Ying, J. Synthesis of 3-trifluoroethylfurans by palladium-catalyzed cyclization-isomerization of (z)-2-alkynyl-3-trifluoromethyl allylic alcohols. J. Org. Chem., 2000, 65, 2003-2006.
    • (2000) J. Org. Chem , vol.65 , pp. 2003-2006
    • Qing, F.1    Gao, W.2    Ying, J.3
  • 57
    • 73349139501 scopus 로고    scopus 로고
    • Palladium-catalyzed sequential reactions via allene intermediates for the rapid synthesis of fused polycyclic pyrrole derivatives
    • Huang, X.; Zhu, S.; Shen, R Palladium-catalyzed sequential reactions via allene intermediates for the rapid synthesis of fused polycyclic pyrrole derivatives. Adv. Synth. Catal. 2009, 351, 3118-3122.
    • (2009) Adv. Synth. Catal , vol.351 , pp. 3118-3122
    • Huang, X.1    Zhu, S.2    Shen, R.3
  • 58
    • 33745725886 scopus 로고    scopus 로고
    • Cascade reactions:Sequential homobimetallic catalysis leading to benzofurans and (3,y-unsaturated esters
    • Gabriele, B.; Mancuso, R; Salerno, G.; Costa, M. Cascade reactions:sequential homobimetallic catalysis leading to benzofurans and (3,y-unsaturated esters. Adv. Synth. Catal. 2006, 348, 1101-1109.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 1101-1109
    • Gabriele, B.1    Mancuso, R.2    Salerno, G.3    Costa, M.4
  • 59
    • 36649034462 scopus 로고    scopus 로고
    • Cascade reactions: A new synthesis of 2-benzofuran-2-ylacetamides by sequential pd(0)-catalyzed deallylation-pd(ii)-catalyzed aminocarbonylative heterocyclization of 1-(2-allyloxyaryl)-2-yn-1-ols
    • Gabriele, B.; Mancuso, R; Salerno, G.; Costa, M. Cascade reactions: a new synthesis of 2-benzofuran-2-ylacetamides by sequential pd(0)-catalyzed deallylation-pd(ii)-catalyzed aminocarbonylative heterocyclization of 1-(2-allyloxyaryl)-2-yn-1-ols. J. Org. Chem. 2007, 72, 9278-9282.
    • (2007) J. Org. Chem , vol.72 , pp. 9278-9282
    • Gabriele, B.1    Mancuso, R.2    Salerno, G.3    Costa, M.4
  • 60
    • 12744274567 scopus 로고    scopus 로고
    • Sequential homobimetallic catalysis: An unprecedented tandem pd(0)-catalysed deprotection - pd(ii)-catalysed heterocyclisation reaction leading to benzofurans
    • Gabriele, B.; Mancuso, R.; Salernob, G.; Veltri, L. Sequential homobimetallic catalysis: an unprecedented tandem pd(0)-catalysed deprotection - pd(ii)-catalysed heterocyclisation reaction leading to benzofurans. Chem. Commun. 2005, 271-273.
    • (2005) Chem. Commun , pp. 271-273
    • Gabriele, B.1    Mancuso, R.2    Salernob, G.3    Veltri, L.4
  • 61
    • 0035799876 scopus 로고    scopus 로고
    • Palladium-mediated intramolecular carbonylative annulation of o-alkynylphenols to synthesize benzo[b]furo[3,4-d]furan-1-ones
    • Hu, Y.; Yang, Z. Palladium-mediated intramolecular carbonylative annulation of o-alkynylphenols to synthesize benzo[b]furo[3,4-d]furan-1-ones. Org. Lett. 2001, 3, 1387-1390.
    • (2001) Org. Lett , vol.3 , pp. 1387-1390
    • Hu, Y.1    Yang, Z.2
  • 62
    • 0034685919 scopus 로고    scopus 로고
    • Palladium-catalyzed reaction of propargyl nucleophiles with β-sulfonyl ct,β-unsaturated ketones: A single-step synthesis of furo[3,4-c] heterocyclic derivatives
    • Monteiro, N.; Balme, G. Palladium-catalyzed reaction of propargyl nucleophiles with β-sulfonyl ct,β-unsaturated ketones: a single-step synthesis of furo[3,4-c] heterocyclic derivatives. J. Org. Chem. 2000, 65, 3223-3226.
    • (2000) J. Org. Chem , vol.65 , pp. 3223-3226
    • Monteiro, N.1    Balme, G.2
  • 64
    • 0037189249 scopus 로고    scopus 로고
    • Efficient and general synthesis of 5-(alkoxycarbonyl)methylene-3-oxazolines by palladium-catalyzed oxidative carbonylation of prop-2-ynylamides
    • Bacchi, A.; Costa, M.; Gabriele, B.; Pelizzi, G.; Salerno, G. Efficient and general synthesis of 5-(alkoxycarbonyl)methylene-3-oxazolines by palladium-catalyzed oxidative carbonylation of prop-2-ynylamides. J. Org. Chem. 2002, 67, 4450-4457.
    • (2002) J. Org. Chem , vol.67 , pp. 4450-4457
    • Bacchi, A.1    Costa, M.2    Gabriele, B.3    Pelizzi, G.4    Salerno, G.5
  • 65
    • 0000747680 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed tandem intramolecular aminopalladation of alkynes and conjugate addition. synthesis of oxazolidinones, imidazolidinones, and lactams
    • Lei, A.; Lu, X. Palladium(II)-catalyzed tandem intramolecular aminopalladation of alkynes and conjugate addition. synthesis of oxazolidinones, imidazolidinones, and lactams. Org. Lett. 2000, 2, 2699-2702.
    • (2000) Org. Lett , vol.2 , pp. 2699-2702
    • Lei, A.1    Lu, X.2
  • 66
    • 51049092976 scopus 로고    scopus 로고
    • Ag-mediated reactions: Coupling and heterocyclization reactions
    • Weibel, J.; Blanc, A.; Pale, P. Ag-mediated reactions: coupling and heterocyclization reactions. Chem. Rev. 2008, 108, 3149-3173;
    • (2008) Chem. Rev , vol.108 , pp. 3149-3173
    • Weibel, J.1    Blanc, A.2    Pale, P.3
  • 67
    • 51049115331 scopus 로고    scopus 로고
    • Asymmetric silver-catalyzed reactions
    • Naodovic, M.; Yamamoto, H. Asymmetric silver-catalyzed reactions. Chem. Rev. 2008, 108, 3132-3148;
    • (2008) Chem. Rev , vol.108 , pp. 3132-3148
    • Naodovic, M.1    Yamamoto, H.2
  • 68
    • 51049091432 scopus 로고    scopus 로고
    • sp-Si Bond Transformations and Related Processes
    • Yamamoto, Y. Silver-Catalyzed Csp-H and Csp-Si Bond Transformations and Related Processes. Chem. Rev. 2008, 108, 3199-3222;
    • (2008) Chem. Rev , vol.108 , pp. 3199-3222
    • Yamamoto, Y.1
  • 69
    • 51049085597 scopus 로고    scopus 로고
    • Ignacio, R silver-mediated synthesis of heterocycles
    • Miriam, A.; Manuel, M.; Ignacio, R silver-mediated synthesis of heterocycles. Chem. Rev. 2008,108, 3174-3198.
    • (2008) Chem. Rev , vol.108 , pp. 3174-3198
    • Miriam, A.1    Manuel, M.2
  • 70
    • 51049123834 scopus 로고    scopus 로고
    • CuH-catalyzed reactions
    • Deutsch, C; Krause, N. CuH-catalyzed reactions. Chem. Rev. 2008, 108, 2916-2927;
    • (2008) Chem. Rev , vol.108 , pp. 2916-2927
    • Deutsch, C.1    Krause, N.2
  • 71
    • 34250694837 scopus 로고    scopus 로고
    • Heterocycle synthesis by copper facilitated addition of heteroatoms to alkenes, alkynes and arenes
    • Chemler, S. R; Fuller, P. H. Heterocycle synthesis by copper facilitated addition of heteroatoms to alkenes, alkynes and arenes. Chem. Soc. Rev. 2007, 36, 1153-1160;
    • (2007) Chem. Soc. Rev , vol.36 , pp. 1153-1160
    • Chemler, S.R.1    Fuller, P.H.2
  • 72
    • 51049124509 scopus 로고    scopus 로고
    • Directed Reactions of Organocopper Reagents
    • Breit, B.; Schmidt, Y. Directed Reactions of Organocopper Reagents. Chem. Rev. 2008,108, 2928-2951.
    • (2008) Chem. Rev , vol.108 , pp. 2928-2951
    • Breit, B.1    Schmidt, Y.2
  • 74
    • 45149147297 scopus 로고    scopus 로고
    • Silver(I)-catalyzed facile synthesis of pyrazoles from propargyl n-sulfonylhydrazones
    • Lee, Y.; Chung, Y. Silver(I)-catalyzed facile synthesis of pyrazoles from propargyl n-sulfonylhydrazones. J. Org. Chem. 2008, 73, 4698-4701.
    • (2008) J. Org. Chem , vol.73 , pp. 4698-4701
    • Lee, Y.1    Chung, Y.2
  • 75
    • 34548158479 scopus 로고    scopus 로고
    • Base- and ligand-free room-temperature synthesis of n-fused heteroaromatic compounds via the transition metal-catalyzed cycloisomerization protocol
    • Seregin, I. V.; Schammel, L. W.; Gevorgyan, V. Base- and ligand-free room-temperature synthesis of n-fused heteroaromatic compounds via the transition metal-catalyzed cycloisomerization protocol. Org. Lett. 2007, 9, 3433-3436.
    • (2007) Org. Lett , vol.9 , pp. 3433-3436
    • Seregin, I.V.1    Schammel, L.W.2    Gevorgyan, V.3
  • 76
    • 68149120414 scopus 로고    scopus 로고
    • 6
    • Ji, K.; Shu, X.; Zhao, S.; Zhu, H.; Niu, Y.; Liu, X.; Liang, Y. Novel carbon-carbon bond formation from propargylic alcohols and olefin toward five-membered heterocyclic rings catalyzed by agsbf6. Org. Lett. 2009, 11, 3206-3209.
    • (2009) Org. Lett , vol.11 , pp. 3206-3209
    • Ji, K.1    Shu, X.2    Zhao, S.3    Zhu, H.4    Niu, Y.5    Liu, X.6    Liang, Y.7
  • 77
    • 35548985413 scopus 로고    scopus 로고
    • Selective synthesis of fluorinated furan derivatives via agno3-catalyzed activation of an electronically deficient triple bond
    • Arimitsu, S.; Hammond, G. B. Selective synthesis of fluorinated furan derivatives via agno3-catalyzed activation of an electronically deficient triple bond. J. Org. Chem. 2007, 72, 8559-8561.
    • (2007) J. Org. Chem , vol.72 , pp. 8559-8561
    • Arimitsu, S.1    Hammond, G.B.2
  • 78
    • 14344254459 scopus 로고    scopus 로고
    • Silver-catalyzed hydroamination: Synthesis of n-bridgehead pyrroles, incorporating a protection-deprotection strategy for preparation of cyclic secondary vinylogous carbamates
    • Robinson, R. S.; Dovey, M. C.; Gravestock, D. Silver-catalyzed hydroamination: synthesis of n-bridgehead pyrroles, incorporating a protection-deprotection strategy for preparation of cyclic secondary vinylogous carbamates. Eur. J. Org. Chem. 2005, 505-511.
    • (2005) Eur. J. Org. Chem , pp. 505-511
    • Robinson, R.S.1    Dovey, M.C.2    Gravestock, D.3
  • 79
    • 66249147550 scopus 로고    scopus 로고
    • Silver(I)-catalyzed cascade: Direct access to furans from alkynyloxiranes
    • Blanc, A.; Tenbrink, K.; Weibel, J.; Pale, P. Silver(I)-catalyzed cascade: direct access to furans from alkynyloxiranes. J. Org. Chem. 2009, 74, 4360-4363.
    • (2009) J. Org. Chem , vol.74 , pp. 4360-4363
    • Blanc, A.1    Tenbrink, K.2    Weibel, J.3    Pale, P.4
  • 80
    • 0035819945 scopus 로고    scopus 로고
    • A Novel cu-assisted cycloisomerization of alkynyl imines: Efficient synthesis of pyrroles and pyrrole-containing heterocycles
    • Kelin, A. V.; Sromek, A. W.; Gevorgyan, V. A Novel cu-assisted cycloisomerization of alkynyl imines: efficient synthesis of pyrroles and pyrrole-containing heterocycles. J. Am. Chem. Soc. 2001, 123, 2074-2075.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 2074-2075
    • Kelin, A.V.1    Sromek, A.W.2    Gevorgyan, V.3
  • 81
    • 0347812063 scopus 로고    scopus 로고
    • Double cycloisomerization as a novel and expeditious route to tricyclic heteroaromatic compounds: Short and highly diastereoselective synthesis of (±)-tetraponerine t6
    • Kim, J. T.; Gevorgyan, V. Double cycloisomerization as a novel and expeditious route to tricyclic heteroaromatic compounds: short and highly diastereoselective synthesis of (±)-tetraponerine t6. Org. Lett. 2002, 4, 4697-4699.
    • (2002) Org. Lett , vol.4 , pp. 4697-4699
    • Kim, J.T.1    Gevorgyan, V.2
  • 82
    • 4043175420 scopus 로고    scopus 로고
    • Highly diastereoselective approach toward (±)-tetraponerine t6 and analogues via the double cycloisomerization-reduction of bis-alkynylpyrimidines
    • Kim, J. T.; Butt, J.; Gevorgyan, V. Highly diastereoselective approach toward (±)-tetraponerine t6 and analogues via the double cycloisomerization-reduction of bis-alkynylpyrimidines. J. Org. Chem. 2004, 69, 5638-5645.
    • (2004) J. Org. Chem , vol.69 , pp. 5638-5645
    • Kim, J.T.1    Butt, J.2    Gevorgyan, V.3
  • 83
    • 0037059436 scopus 로고    scopus 로고
    • Efficient synthesis of 2-mono- and 2,5-disubstituted furans via the cui-catalyzed cycloisomerization of alkynyl ketones
    • Kelin, A.V.; Gevorgyan, V. Efficient synthesis of 2-mono- and 2,5-disubstituted furans via the cui-catalyzed cycloisomerization of alkynyl ketones. J. Org. Chem. 2002, 67, 95-98.
    • (2002) J. Org. Chem , vol.67 , pp. 95-98
    • Kelin, A.V.1    Gevorgyan, V.2
  • 84
    • 0037414928 scopus 로고    scopus 로고
    • 1,2-migration of the thio group in allenyl sulfides: Efficient synthesis of 3-thio-substituted furans and pyrroles
    • Kim, J. T.; Kelin, A.V.; Gevorgyan, V. 1,2-migration of the thio group in allenyl sulfides: efficient synthesis of 3-thio-substituted furans and pyrroles. Angew. Chem. Int. Ed. 2003, 42, 98-101.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 98-101
    • Kim, J.T.1    Kelin, A.V.2    Gevorgyan, V.3
  • 85
    • 4544333104 scopus 로고    scopus 로고
    • A novel 1,2-migration of acyloxy, phosphatyloxy, and sulfonyloxy groups in allenes: Efficient synthesis of tri- and tetrasubstituted furans
    • Sromek, A. W.; Kelin, A.V.; Gevorgyan, V. A novel 1,2-migration of acyloxy, phosphatyloxy, and sulfonyloxy groups in allenes: efficient synthesis of tri- and tetrasubstituted furans. Angew. Chem. Int. Ed. 2004, 43, 2280-2282.
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 2280-2282
    • Sromek, A.W.1    Kelin, A.V.2    Gevorgyan, V.3
  • 86
    • 38649108487 scopus 로고    scopus 로고
    • Metal-catalyzed 1,2-shift of diverse migrating groups in allenyl systems as a new paradigm toward densely functionalized heterocycles
    • Dudnik, A. S.; Sromek, A. W.; Rubina, M.; Kim, J. T.; Kelin, A.V.; Gevorgyan, V. Metal-catalyzed 1,2-shift of diverse migrating groups in allenyl systems as a new paradigm toward densely functionalized heterocycles. J. Am. Chem. Soc. 2008, 130, 1440-1452.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 1440-1452
    • Dudnik, A.S.1    Sromek, A.W.2    Rubina, M.3    Kim, J.T.4    Kelin, A.V.5    Gevorgyan, V.6
  • 87
    • 34848915424 scopus 로고    scopus 로고
    • Highly efficient synthesis of functionalized indolizines and indolizinones by copper-catalyzed cycloisomerizations of propargylic pyridines
    • Yan, B.; Zhou, Y.; Zhang, H.; Chen, J.; Liu, Y. Highly efficient synthesis of functionalized indolizines and indolizinones by copper-catalyzed cycloisomerizations of propargylic pyridines. J. Org. Chem. 2007, 72, 7783-7786.
    • (2007) J. Org. Chem , vol.72 , pp. 7783-7786
    • Yan, B.1    Zhou, Y.2    Zhang, H.3    Chen, J.4    Liu, Y.5
  • 88
    • 34948881697 scopus 로고    scopus 로고
    • Copper(II) triflate-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes. a straightforward synthetic route to polysubstituted furans
    • Zhan, Z.; Wang, S.; Cai, X.; Liu, H.; Yu, J.; Cui, Y. Copper(II) triflate-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes. a straightforward synthetic route to polysubstituted furans. Adv. Synth. Catal. 2007, 349, 2097-2102.
    • (2007) Adv. Synth. Catal , vol.349 , pp. 2097-2102
    • Zhan, Z.1    Wang, S.2    Cai, X.3    Liu, H.4    Yu, J.5    Cui, Y.6
  • 89
    • 60849118120 scopus 로고    scopus 로고
    • 2-catalyzed propargylation/cycloisomerization tandem reaction
    • Pan, Y.; Zhao, S.; Ji, W.; Zhan, Z. One-pot synthesis of substituted furans using cu(otf)2-catalyzed propargylation/cycloisomerization tandem reaction. J. Comb. Chem. 2009,11, 103-109.
    • (2009) J. Comb. Chem , vol.11 , pp. 103-109
    • Pan, Y.1    Zhao, S.2    Ji, W.3    Zhan, Z.4
  • 90
    • 0038112039 scopus 로고    scopus 로고
    • Novel ruthenium- and platinum-catalyzed sequential reactions: Synthesis of tri- and tetrasubstituted furans and pyrroles from propargylic alcohols and ketones
    • Nishibayashi, Y.; Yoshikawa, M.; Inada, Y.; Milton, M. D.; Hidai, M.; Uemura, S. Novel ruthenium- and platinum-catalyzed sequential reactions: synthesis of tri- and tetrasubstituted furans and pyrroles from propargylic alcohols and ketones. Angew. Chem. Int. Ed. 2003, 42, 2681-2684.
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 2681-2684
    • Nishibayashi, Y.1    Yoshikawa, M.2    Inada, Y.3    Milton, M.D.4    Hidai, M.5    Uemura, S.6
  • 91
    • 33947607969 scopus 로고    scopus 로고
    • Pt-catalyzed cyclization/1,2-migration for the synthesis of indolizines, pyrrolones, and indolizinones
    • Smith, C. R.; Bunnelle, E. M.; Rhodes, A. J.; Sarpong, R. Pt-catalyzed cyclization/1,2-migration for the synthesis of indolizines, pyrrolones, and indolizinones. Org. Lett. 2007, 9, 1169-1171.
    • (2007) Org. Lett , vol.9 , pp. 1169-1171
    • Smith, C.R.1    Bunnelle, E.M.2    Rhodes, A.J.3    Sarpong, R.4
  • 92
    • 33750033597 scopus 로고    scopus 로고
    • 3-catalyzed nucleophilic substitution of propargylic alcohols
    • Zhan, Z.; Yu, J.; Liu, H.; Cui, Y.; Yang, R.; Yang, W.; Li, J. A general and efficient fecl3-catalyzed nucleophilic substitution of propargylic alcohols. J. Org. Chem. 2006, 71, 8298-8301.
    • (2006) J. Org. Chem , vol.71 , pp. 8298-8301
    • Zhan, Z.1    Yu, J.2    Liu, H.3    Cui, Y.4    Yang, R.5    Yang, W.6    Li, J.7
  • 93
    • 36849027182 scopus 로고    scopus 로고
    • 3-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes
    • Zhan, Z.; Cai, X.; Wang, S.; Yu, J.; Liu, H.; Cui, Y. FeCl3-catalyzed nucleophilic substitution of propargylic acetates with enoxysilanes. J. Org. Chem. 2007, 72, 9838-9841.
    • (2007) J. Org. Chem , vol.72 , pp. 9838-9841
    • Zhan, Z.1    Cai, X.2    Wang, S.3    Yu, J.4    Liu, H.5    Cui, Y.6
  • 94
    • 57649159510 scopus 로고    scopus 로고
    • 3-catalyzed propargylation-cycloisomerization tandem reaction: A facile one-pot synthesis of substitutedfurans
    • Ji, W.; Pan, Y.; Zhao, S.; Zhan, Z. FeCl3-catalyzed propargylation-cycloisomerization tandem reaction: a facile one-pot synthesis of substitutedfurans. Synlett, 2008,19, 3046-3052.
    • (2008) Synlett , vol.19 , pp. 3046-3052
    • Ji, W.1    Pan, Y.2    Zhao, S.3    Zhan, Z.4
  • 95
    • 67649494470 scopus 로고    scopus 로고
    • 2o system
    • Yoshimatsu, M.; Yamamoto, T.; Sawa, A.; Kato, T.; Tanabe, G.; Muraoka, O. α-Sulfanyl and α-selanyl propadienyl cations: regioselective generations and cycloadditions with thioamides and selemides controlled by meno2-h2o system. Org. Lett. 2009,11, 2952-2955.
    • (2009) Org. Lett , vol.11 , pp. 2952-2955
    • Yoshimatsu, M.1    Yamamoto, T.2    Sawa, A.3    Kato, T.4    Tanabe, G.5    Muraoka, O.6
  • 96
    • 3042713083 scopus 로고    scopus 로고
    • Zn(II)/amine-catalyzed coupling reaction of alkylidenemalonates with propargyl alcohol: A one-pot synthesis of methylenetetrahydrofurans
    • Nakamura, M.; Liang, C; Nakamura, E. Zn(II)/amine-catalyzed coupling reaction of alkylidenemalonates with propargyl alcohol: a one-pot synthesis of methylenetetrahydrofurans. Org. Lett. 2004, 6, 2015-2017.
    • (2004) Org. Lett , vol.6 , pp. 2015-2017
    • Nakamura, M.1    Liang, C.2    Nakamura, E.3
  • 97
    • 64649100098 scopus 로고    scopus 로고
    • 6-mediated intramolecular pauson-khand reaction of substituted diethyl 3-allyloxy-1-propynylphosphonates
    • Moradov, D.; Quntar, A.; Youssef, M.; Smoum, R; Rubinstein, A.; Srebnik, M. Mo(CO)6-mediated intramolecular pauson-khand reaction of substituted diethyl 3-allyloxy-1-propynylphosphonates. J. Org. Chem. 2009, 74, 1029-1033.
    • (2009) J. Org. Chem , vol.74 , pp. 1029-1033
    • Moradov, D.1    Quntar, A.2    Youssef, M.3    Smoum, R.4    Rubinstein, A.5    Srebnik, M.6
  • 98
    • 70349783633 scopus 로고    scopus 로고
    • Addition-hydroamination reactions of propargyl cyanamides: Rapid access to highly substituted 2-aminoimidazoles
    • Giles, R L.; Sullivan, J. D.; Steiner, A. M.; Looper, R E. Addition-hydroamination reactions of propargyl cyanamides: rapid access to highly substituted 2-aminoimidazoles. Angew. Chem. Int. Ed. 2009,48, 3116-3120.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 3116-3120
    • Giles, R.L.1    Sullivan, J.D.2    Steiner, A.M.3    Looper, R.E.4
  • 99
    • 73449114976 scopus 로고    scopus 로고
    • Synthesis of 2-thio- and 2-oxoimidazoles via cascade addition-cycloisomerization reactions of propargylcyanamides
    • Giles, R L.; Nkansah, R A.; Looper, R E. Synthesis of 2-thio- and 2-oxoimidazoles via cascade addition-cycloisomerization reactions of propargylcyanamides. J. Org. Chem. 2010, 75, 261-264.
    • (2010) J. Org. Chem , vol.75 , pp. 261-264
    • Giles, R.L.1    Nkansah, R.A.2    Looper, R.E.3
  • 100
    • 77749298192 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (-)-α-kainic Acid
    • Farwick, A.; Helmchen, G. Enantioselective total synthesis of (-)-α-kainic Acid. Org. Lett. 2010,12, 1108-1111.
    • (2010) Org. Lett , vol.12 , pp. 1108-1111
    • Farwick, A.1    Helmchen, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.