English

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• 1. [1] (a) J.M. Holub, K. Kirshenbaum, Tricks with clicks: modification of peptidomimetic oligomers via copper-catalyzed azide-alkyne [3+2] cycloaddition, Chem. Soc. Rev. 39 (2010) 1325-1337; (b) A. Soules, B. Ameduri, B. Boutevin, G. Calleja, Original fluorinated copolymers achieved by both azide/alkyne "click" reaction and Hay coupling from tetrafluoroethylene telomers, Macromolecules 43 (2010) 4489-4499; (c) Z.W. Chen, D.N. Ye, Y.P. Qian, M. Ye, L.X. Liu, Highly efficient AgBF₄-catalyzed synthesis of methyl ketones from terminal alkynes, Tetrahedron 69 (2013) 6116- 6120; (d) S. Bew, G. Hiatt-Gipson, J.A. Lovell, C. Poullain, Mild reaction conditions for the terminal deuteration of alkynes, Org. Lett. 14 (2012) 456-459; (e) Z.M. Dong, Z.B. Ye, Synthesis of hyperbranched poly(phenylacetylene)s containing pendant alkyne groups by one-pot Pd-catalyzed copolymerization of phenylacetylene with diynes, Macromolecules 45 (2012) 5020-5031; (f) N. Onishi, M. Shiotsuki, T. Masuda, N. Sano, F. Sanda, Polymerization of phenylacetylenes using rhodium catalysts coordinated by norbornadiene linked to a phosphino or amino group, Organometallics 32 (2013) 846-853; (g) B.W. Zhou, H. Chen, C.Y. Wang, Mn-catalyzed aromatic C-H alkenylation with terminal alkynes, J. Am. Chem. Soc. 135 (2013) 1264-1267.[1] (a) J.M. Holub, K. Kirshenbaum, Tricks with clicks: modification of peptidomimetic oligomers via copper-catalyzed azide-alkyne [3+2] cycloaddition, Chem. Soc. Rev. 39 (2010) 1325-1337; (b) A. Soules, B. Ameduri, B. Boutevin, G. Calleja, Original fluorinated copolymers achieved by both azide/alkyne "click" reaction and Hay coupling from tetrafluoroethylene telomers, Macromolecules 43 (2010) 4489-4499; (c) Z.W. Chen, D.N. Ye, Y.P. Qian, M. Ye, L.X. Liu, Highly efficient AgBF₄-catalyzed synthesis of methyl ketones from terminal alkynes, Tetrahedron 69 (2013) 6116- 6120; (d) S. Bew, G. Hiatt-Gipson, J.A. Lovell, C. Poullain, Mild reaction conditions for the terminal deuteration of alkynes, Org. Lett. 14 (2012) 456-459; (e) Z.M. Dong, Z.B. Ye, Synthesis of hyperbranched poly(phenylacetylene)s containing pendant alkyne groups by one-pot Pd-catalyzed copolymerization of phenylacetylene with diynes, Macromolecules 45 (2012) 5020-5031; (f) N. Onishi, M. Shiotsuki, T. Masuda, N. Sano, F. Sanda, Polymerization of phenylacetylenes using rhodium catalysts coordinated by norbornadiene linked to a phosphino or amino group, Organometallics 32 (2013) 846-853; (g) B.W. Zhou, H. Chen, C.Y. Wang, Mn-catalyzed aromatic C-H alkenylation with terminal alkynes, J. Am. Chem. Soc. 135 (2013) 1264-1267.

  2. [2] (a) A. Zarei, One-pot, efficient, and regioselective syntheses of 1,4-disubstituted 1,2,3-triazoles using aryldiazonium silica sulfates in water, Tetrahedron Lett. 53 (2012) 5176-5179; (b) W.S. Zhang, C.X. Kuang, Q. Yang, Synthesis of phenyl azides bearing (E)-2- halovinyl group, Res. Chem. Intermed. 38 (2012) 37-44; (c) Z.Z. Huang, R.L. Wang, S.R. Sheng, R.Y. Zhou, M.Z. Cai, Preparation of polystyrene- supported vinyl sulfone and its application in the solid-phase organic synthesis of 1-monosubstituted 1,2,3-triazoles, React. Funct. Polym. 73 (2013) 224-227; (d) Q. Yang, Y.B. Jiang, C.X. Kuang, Facile one-pot synthesis of monosubstituted 1- aryl-1H-1,2,3-triazoles from arylboronic acids and prop-2-ynoic acid (=propiolic acid) or calcium acetylide (=calcium carbide) as acetylene source, Helv. Chim. Acta 95 (2012) 448-454; (e) M. Xu, C.X. Kuang, Z. Wang, Q. Yang, Y.B. Jiang, A novel approach to 1- monosubstituted 1,2,3-triazoles by a click cycloaddition/decarboxylation process, Synthesis (2011) 223-228; (f) Y.B. Jiang, C.X. Kuang, Q. Yang, Facile and quick synthesis of 1-monosubstituted aryl 1,2,3-triazoles: a copper-free [3+2] cycloaddition, Tetrahedron 67 (2011) 289-292; (g) L. Wu, Y. Xie, Z. Chen, Y. Niu, Y. Liang, A convenient synthesis of 1-substituted 1,2,3-triazoles via CuI/Et₃N catalyzed ‘click chemistry' from azides and acetylene gas, Synlett (2009) 1453-1456.[2] (a) A. Zarei, One-pot, efficient, and regioselective syntheses of 1,4-disubstituted 1,2,3-triazoles using aryldiazonium silica sulfates in water, Tetrahedron Lett. 53 (2012) 5176-5179; (b) W.S. Zhang, C.X. Kuang, Q. Yang, Synthesis of phenyl azides bearing (E)-2- halovinyl group, Res. Chem. Intermed. 38 (2012) 37-44; (c) Z.Z. Huang, R.L. Wang, S.R. Sheng, R.Y. Zhou, M.Z. Cai, Preparation of polystyrene- supported vinyl sulfone and its application in the solid-phase organic synthesis of 1-monosubstituted 1,2,3-triazoles, React. Funct. Polym. 73 (2013) 224-227; (d) Q. Yang, Y.B. Jiang, C.X. Kuang, Facile one-pot synthesis of monosubstituted 1- aryl-1H-1,2,3-triazoles from arylboronic acids and prop-2-ynoic acid (=propiolic acid) or calcium acetylide (=calcium carbide) as acetylene source, Helv. Chim. Acta 95 (2012) 448-454; (e) M. Xu, C.X. Kuang, Z. Wang, Q. Yang, Y.B. Jiang, A novel approach to 1- monosubstituted 1,2,3-triazoles by a click cycloaddition/decarboxylation process, Synthesis (2011) 223-228; (f) Y.B. Jiang, C.X. Kuang, Q. Yang, Facile and quick synthesis of 1-monosubstituted aryl 1,2,3-triazoles: a copper-free [3+2] cycloaddition, Tetrahedron 67 (2011) 289-292; (g) L. Wu, Y. Xie, Z. Chen, Y. Niu, Y. Liang, A convenient synthesis of 1-substituted 1,2,3-triazoles via CuI/Et₃N catalyzed ‘click chemistry' from azides and acetylene gas, Synlett (2009) 1453-1456.

  3. [3] (a) Y.Y. Liu, C.P. Wang, X.B. Wang, J.P. Wan, Enaminone ligand-assisted homoand cross-coupling of terminal alkynes under mild conditions, Tetrahedron Lett. 54 (2013) 3953-3955; (b) D.H. Bai, C.J. Li, J. Li, X.S. Jia, New progress of acetylene-coupling reactions, Chin. J. Org. Chem. 32 (2012) 994-1009; (c) X.J. Niu, C.J. Li, J. Li, X.S. Jia, Importance of bases on the copper-catalyzed oxidative homocoupling of terminal alkynes to 1,4-disubstituted 1,3-diynes, Tetrahedron Lett. 53 (2012) 5559-5561; (d) L.L. Li, C.Y. Nan, Q. Peng, Y.D. Li, Selective synthesis of Cu₂O nanocrystals as shape-dependent catalysts for oxidative arylation of phenylacetylene, Chem. Eur. J. 18 (2012) 10491-10496; (e) Z.Q. Weng, H.F. Li, W.M. He, et al., Mild copper-catalyzed trifluoromethylation of terminal alkynes using an electrophilic trifluoromethylating reagent, Tetrahedron 68 (2012) 2527-2531; (f) S.S. Patil, R.P. Jadhav, S.V. Patil, V.D. Bobade, Ligand and solvent-free iron catalyzed oxidative alkynylation of azoles with terminal alkynes, Tetrahedron Lett. 52 (2011) 5617-5619; (g) X.P. Nie, S.L. Liu, Y. Zong, P.P. Sun, J.C. Bao, Facile synthesis of substituted alkynes by nano-palladium catalyzed oxidative cross-coupling reaction of arylboronic acids with terminal alkynes, J. Organomet. Chem. 696 (2011) 1570-1573; (h) H. Xu, S.J. Gu, W.Z. Chen, D.C. Li, J.M. Dou, TBAF-mediated reactions of 1,1- dibromo-1-alkenes with thiols and amines and regioselective synthesis of 1,2- heterodisubstituted alkenes, J. Org. Chem. 76 (2011) 2448-2458; (i) B. Movassagh, M. Navidi, A simple and effective approach to the synthesis of alkynyl selenides from terminal alkynes, Chin. Chem. Lett. 23 (2012) 1035-1038; (j) Q.F. Zhou, X.P. Chu, S. Zhao, T. Lu, W.F. Tang, BF₃·Et₂O promoted conjugate addition of ethanethiol to electron-deficient alkynes, Chin. Chem. Lett. 23 (2012) 639-642; (k) M. Bakherad, A. Amin, A. Keivanloo, B. Bahramian, M. Raessi, Using Pd-salen complex as an efficient catalyst for the copper- and solvent-free coupling of acyl chlorides with terminal alkynes under aerobic conditions, Chin. Chem. Lett. 21 (2010) 656-660.[3] (a) Y.Y. Liu, C.P. Wang, X.B. Wang, J.P. Wan, Enaminone ligand-assisted homoand cross-coupling of terminal alkynes under mild conditions, Tetrahedron Lett. 54 (2013) 3953-3955; (b) D.H. Bai, C.J. Li, J. Li, X.S. Jia, New progress of acetylene-coupling reactions, Chin. J. Org. Chem. 32 (2012) 994-1009; (c) X.J. Niu, C.J. Li, J. Li, X.S. Jia, Importance of bases on the copper-catalyzed oxidative homocoupling of terminal alkynes to 1,4-disubstituted 1,3-diynes, Tetrahedron Lett. 53 (2012) 5559-5561; (d) L.L. Li, C.Y. Nan, Q. Peng, Y.D. Li, Selective synthesis of Cu₂O nanocrystals as shape-dependent catalysts for oxidative arylation of phenylacetylene, Chem. Eur. J. 18 (2012) 10491-10496; (e) Z.Q. Weng, H.F. Li, W.M. He, et al., Mild copper-catalyzed trifluoromethylation of terminal alkynes using an electrophilic trifluoromethylating reagent, Tetrahedron 68 (2012) 2527-2531; (f) S.S. Patil, R.P. Jadhav, S.V. Patil, V.D. Bobade, Ligand and solvent-free iron catalyzed oxidative alkynylation of azoles with terminal alkynes, Tetrahedron Lett. 52 (2011) 5617-5619; (g) X.P. Nie, S.L. Liu, Y. Zong, P.P. Sun, J.C. Bao, Facile synthesis of substituted alkynes by nano-palladium catalyzed oxidative cross-coupling reaction of arylboronic acids with terminal alkynes, J. Organomet. Chem. 696 (2011) 1570-1573; (h) H. Xu, S.J. Gu, W.Z. Chen, D.C. Li, J.M. Dou, TBAF-mediated reactions of 1,1- dibromo-1-alkenes with thiols and amines and regioselective synthesis of 1,2- heterodisubstituted alkenes, J. Org. Chem. 76 (2011) 2448-2458; (i) B. Movassagh, M. Navidi, A simple and effective approach to the synthesis of alkynyl selenides from terminal alkynes, Chin. Chem. Lett. 23 (2012) 1035-1038; (j) Q.F. Zhou, X.P. Chu, S. Zhao, T. Lu, W.F. Tang, BF₃·Et₂O promoted conjugate addition of ethanethiol to electron-deficient alkynes, Chin. Chem. Lett. 23 (2012) 639-642; (k) M. Bakherad, A. Amin, A. Keivanloo, B. Bahramian, M. Raessi, Using Pd-salen complex as an efficient catalyst for the copper- and solvent-free coupling of acyl chlorides with terminal alkynes under aerobic conditions, Chin. Chem. Lett. 21 (2010) 656-660.

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  7. [7] (a) X.Z. Cheng, J. Jia, C.X. Kuang, Convenient synthesis of terminal alkynes from anti-3-aryl-2,3-dibromopropanoic acids using a K₂CO₃/DMSO system, Chin. J. Chem. 29 (2011) 2350-2354; (b) S. Shenawi-Khalil, S.U. Sonavane, Y. Sasson, Synthesis of acetylenes via dehydrobromination using solid anhydrous potassium phosphate as the base under phase-transfer conditions, Tetrahedron Lett. 53 (2012) 2295-2297; (c) M. Zhao, C.X. Kuang, Q. Yang, X.Z. Cheng, Cs₂CO₃-mediated synthesis of terminal alkynes from 1,1-dibromo-1-alkenes, Tetrahedron Lett. 52 (2011) 992-994.[7] (a) X.Z. Cheng, J. Jia, C.X. Kuang, Convenient synthesis of terminal alkynes from anti-3-aryl-2,3-dibromopropanoic acids using a K₂CO₃/DMSO system, Chin. J. Chem. 29 (2011) 2350-2354; (b) S. Shenawi-Khalil, S.U. Sonavane, Y. Sasson, Synthesis of acetylenes via dehydrobromination using solid anhydrous potassium phosphate as the base under phase-transfer conditions, Tetrahedron Lett. 53 (2012) 2295-2297; (c) M. Zhao, C.X. Kuang, Q. Yang, X.Z. Cheng, Cs₂CO₃-mediated synthesis of terminal alkynes from 1,1-dibromo-1-alkenes, Tetrahedron Lett. 52 (2011) 992-994.

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