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Publications
2015
8.Chen, Q.; Gao, K. K, Peng, C.;Xie, H. B.; Zhao, Z. B.; Bao, M. Cellulosic poly(ionic liquid)s: synthesis, characterization and application in the cycloaddition of CO2 to epoxides. Rsc .Adv.,2015,5,44598–44603.
8.Chen, Q.; Gao, K. K, Peng, C.;Xie, H. B.; Zhao, Z. B.; Bao, M. Preparation of lignin/glycerol-based bis(cyclic carbonate) for the synthesis of polyurethanes Green Chemistry.,2015,17,4546–4551.
8.Sun Jian,Bao Ming, Feng Xiujuan,Yu Xiaoqiang ,Yamamoto Yoshinori ,I. Almansour Abdulrahman ,Arumugam Natarajan,Suresh Kumar Raju.Tetrahedron Lett.,2015,56,6747–6750.
7.S. Takalea B., Bao M., Yamamoto Y., I. Almansourc A., Arumugam N., S.Kumarc R. Applications of Metal Nanopore Catalysts in Organic Synthesis.Synlett 2015; 26(17): 2355-2380.
6.Jiang H.,Oniw K.,Islamc A.,Zhao J.,Han L.Y.,Sun Y.J.,Bao M.,Asao N.,Yamamoto Y.,Jin T.N.. Efficient thieno[3,2-a]carbazole-based organic dyes for dye-sensitized solar cells. Tetrahedron.,2015,71,6534–6540.
5.Wang, W.H.; Himeda, Y.; Muckerman, J.T.; Manbeck, G.F.; Fujita, E.CO2 Hydrogenation to Formate and Methanol as an Alternative to Photo- and Electrochemical CO2 Reduction. Chem. Rev.,2015,115,12936-12973.
4. Jiang, H.; Ferrara, G.; Zhang, X.,et al. Triflic Acid Mediated Cascade Cyclization of Aryldiynes for the Synthesis of Indeno[1,2-c]chromenes: Application to Dye-Sensitized Solar Cells Chem. Eur. J. 2015, 21, 4065 – 4070.
3. Zhang, S.; Yu, X. Q.; Feng, X. J.; Yamamoto, Y.; Bao, M., Palladium-catalyzed Regioselective Allylation of Five-membered Heteroarenes with Allyltributylstannane. Chem. Commun., 2015,51, 3842.
2. Mayo, M.S.; Yu, X. Q.; Feng, X. J.; Yoshinori Y.; Bao, M., Isoquinolone Synthesis through SNAr Reaction of 2‑Halobenzonitrileswith Ketones Followed by Cyclization. J. Org. Chem. 2015, 80, 3998−4002.
1. Zou, T.; Yu, X. Q.; Feng, X. J Bao, M., An efficient transformation of primary halides intonitriles through palladium-catalyzed hydrogentransfer reaction. Chem. Commun.,2015,51, 10714.
2014
1. Si, W. L.; Lu, S. R.; Asao, N.; Bao, M.; Yamamoto, Y.; Jin, T. N., NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes. Chem. Commun., 2014, 50, 15730-15732.
2. Si, W. L.; Lu, S. R.; Bao, M.; Asao, N.; Yamamoto, Y.; Jin, T. N., Cu-Catalyzed C-H Amination of Hydrofullerenes Leading to 1,4-Difunctionalized Fullerenes. Org. Lett., 2014, 16, 620-623.
3. Zhang, X.; Si, W. L.; Bao, M.; Asao, N.; Yamamoto, Y.; Jin, T. N., Rh(III)-Catalyzed Regioselective Functionalization of C-H Bonds of Naphthylcarbamates for Oxidative Annulation with Alkynes. Org. Lett., 2014, 16, 4830-4833.
4. Takale, B. S.; Tao, S. M.; Yu, X. Q.; Feng, X. J.; Jin, T. N.; Bao, M.; Yamamoto, Y., Highly chemoselective reduction of imines using a AuNPore/PhMe2SiH/water system and its application to reductive amination. Tetrahedron, PagesAhead of Print, DOI:10.1016/j.tet.2014.11.023
5. Takale, B. S.; Wang, S. Q.; Zhang, X.; Feng, X. J.; Yu, X. Q.; Jin, T. N., Bao, M.; Yamamoto, Y., Chemoselective reduction of a,b-unsaturated aldehydes using an unsupported nanoporous gold catalyst. Chem. Commun., 2014, 50, 14401-14404.
6. Sun, J.; Feng, X. J.; Zhao, Z. R.; Yamamoto, Y.; Bao, M., Carbonylative Stille coupling reactions of benzyl chlorides with allyltributylstannane catalyzed by palladium nanoparticles. Tetrahedron, 2014, 70, 7166-7171.
7. Yu, X. Q.; Huang, N.; Feng, X. J.; Yamamoto, Y.; Bao, M., Synthesis of 1,3,5-trisubstituted pyrazoles by the cope-type hydroamination of 1,3-dialkynes with alkylhydrazines. SYNTHESIS-STUTTGART, 2014, 46, 2422-2429.
8. Mayo, M. S.; Yu, X. Q.; Zhou, X. Y.; Feng, X. J.; Yamamoto, Y.; Bao, M., Convenient Synthesis of Benzothiazoles and Benzimidazoles through Bronsted Acid Catalyzed Cyclization of 2-Amino Thiophenols/Anilines with beta-Diketones. Org. Lett., 2014, 16, 764-767
9. Takale, B. S.; Tao, S. M.; Yu, X. Q.; Feng, X. J.; Jin, T. N.; Bao, M.; Yamamoto, Y., Exclusive Chemoselective Reduction of Imines in the Coexistence of Aldehydes Using AuNPore Catalyst. Org. Lett., 2014, 16, 2558-2561.
10. Takale, B. S.; Bao, M.; Yamamoto, Y., Gold nanoparticle (AuNPs) and gold nanopore (AuNPore) catalysts in organic synthesis. Org. Biomol. Chem., 2014, 12, 2005-2027.
11. Zhang, S.; Wang, L. G.; Feng, X. J.; Bao, M., Palladium-catalyzed carbonylative addition of aryl bromides to arylalkynes: a simple and efficient method for chalcone synthesis. Org. Biomol. Chem., 2014, 12, 7233-7237.
12. Muhammad, S. M.; Yu, X. Q.; Zhou, X. Y.; Feng, X. J.; Yamamoto, Y.; Bao, M., Synthesis of Benzoxazoles from 2 Aminophenols and β Diketones Using a Combined Catalyst of Brønsted Acid and Copper Iodide. J. Org. Chem., 2014, 79, 6310-6314.
13. Yu, X. Q.; Ci, Z. H.; Liu, T.; Feng, X. J.; Wang, C. L.; Ma, T. L.; Bao, M., Influence of different electron acceptors in organic sensitizers on the performance of dye-sensitized solar cells. Dyes and Pigments, 2014, 102, 126-132.
14. Ci, Z.H.; Yu, X. Q.; Wang, C. L.; Ma, T. L.; Bao, M., Influence of different substituents linked on fluorene spacer in organic sensitizers on photovoltaic properties. Dyes and Pigments, 2014, 104, 8-14.
2013
1. Yu, X. Q.; Wang, L. G.; Feng, X. J.; Yamamoto, Y., Copper-catalyzed aldol-type addition of ketones to aromatic nitriles: a simple approach to enaminone synthesis. Chem. Commun., 2013, 49, 2885-2887.
2. Zhang, X.; Feng, X. J.; Yu, X. Q.; He, R.; Bao, M., Regio- and chemoselective palladium-catalyzed benzylallylation of activated olefins: the remarkable effect of palladium nanoparticles. Org. Bio. Chem., 2013, 22, 4016-4024.
3. Feng, X. J.; Song, J. L.; Liu, H. S.; Wang, L. G; Yu, X. Q.; Bao, M., Palladium-catalyzed carbonylative coupling of (chloromethyl)arenes with terminal arylalkynes to produce 1,4-diaryl-3-butyn-2-ones. RSC Adv., 2013, 3, 18985-18991.
4. Zou, T.; Feng, X. J.; Liu, H. S.; Yu, X. Q.; Yamamoto, Y.; Bao, M., Efficient palladium-catalyzed cyanation of aryl/heteroaryl bromides with K-4[Fe(CN)(6)] in t-BuOH-H2O using tris(2-morpholinophenyl)phosphine as a ligand. RSC Adv., 2013, 3, 20379-2038
5. Ci, Z. H.; Yu, X. Q.; Bao, M.; Wang, C. L.; Ma, T. L., Influence of the benzo[d]thiazole-derived pi-bridges on the optical and photovoltaic performance of D-pi-A dyes. Dyes and Pigments, 2013, 96, 619-625.
6. Yan, M.; Jin, T. N.; Chen, Q.; Ho, H. E.; Fujita, T.; Chen, L. Y.; Bao, M.; Chen, M. W.; Asao, N.; Yamamoto, Y., Unsupported Nanoporous Gold Catalyst for Highly Selective Hydrogenation of Quinolines. Org. Lett., 2013, 15, 1484-1487.
7. Lu, S. R.; Si, W. L.; Bao, M.; Yamamoto, Y.; Jin, T. N., Co-Catalyzed Radical Cycloaddition of [60]Fullerene with Active Dibromides: Selective Synthesis of Carbocycle-Fused Fullerene Monoadducts. Org. Lett., 2013, 15, 4030-4033.
8. Zhang, X.; Yu, X. Q.; Feng, X. J.; Liu, H. S.; He, R.; Yamamoto, Y.; Bao, M., Regioselective control by a catalyst switch in palladium-catalyzed benzylallylation of arylethylidene malononitriles. J. Organometall. Chem., 2013, 745, 177-185.
9. Feng, X. J.; Sun, A. L.; Zhang, S., Palladium-Catalyzed Carboxylative Coupling of Benzyl Chlorides with Allyltributylstannane: Remarkable Effect of Palladium Nanoparticles. Org. Lett., 2013,15(1), 108-111.
10. Wang, L. G.; Yu, X. Q.; Feng, X. J.;. Synthesis of 3,5-Disubstituted Pyrazoles via Cope-Type Hydroamination of 1,3-Dialkynes. J. Org. Chem., 2013, 78 (4), 1693–1698
11.Qu, Y. P.; Wang, L. X.; Zhou X. Y., Copper-Catalyzed Condensation Reaction of Amines with 1,3-Dicarbonyl Compounds to Produce Enaminones. Chin. J. Org. Chem. 2013, 33(4), 860-865.
2012
1. Zhang X.; Feng X.; Liu H.; Qin Y.; Dai Y., Palladium-Catalyzed Three-Component Coupling Reaction of Benzyl Chlorides, Allyltributylstannane, and Carbon Monoxide: Efficient Synthesis of α,β-Unsaturated Ketones. Chin. J. Catal. 2012, 33, (3), 523-529.
2. Dai, Y.; Feng, X.; Wang, B.; He, R.; Bao, M., Preparation and application of air-stable P,N-bidentate ligands for the selective synthesis of δ-lactone via the palladium-catalyzed telomerization of 1,3-butadiene with carbon dioxide. J. Organometall. Chem. 2012, 696, (26), 4309-4314.
3. Lu, S. R.; Jin, T. N.; Bao, M.; Yamamoto, Y., NaOH-Catalyzed Dimerization of Monofunctionalized Hydrofullerenes: Transition-Metal-Free, General, and Efficient Synthesis of Single-Bonded [60]Fullerene Dimers. Org. Lett., 2012, 14 (13), 3466–3469.
4. Lu, S. R.; Jin, T. N.; Bao, M.; Asiri, A. M.; Yamamoto, Y., Palladium-catalyzed bisfunctionalization of active alkenes by beta-acetonitrile-alpha-allyl addition: application to the synthesis of unsymmetric 1,4-di(organo)fullerene derivatives. Tetrahedron Lett. 2012, 53(10), 1210–1213.
5. Zhang, X.; Yu, X. Q.; Feng, X. J.; Bao, M., Palladium-Catalyzed Direct 1,4-Addition of Heteroarenes to alpha,beta-Unsaturated Ketones via C-H Activation. Synlett. 2012, (11), 1605-1608.
6. Xu, Z. W.; Yu, X. Q.; Feng, X. J.; Bao, M., Arylglycine-derivative synthesis via oxidative sp(3) C-H functionalization of alpha-amino esters. Beilstein J. Org. Chem. 2012, 8, 1564–1568.
7. Zhang, S.; Bao, M. Synthesis of Naphthylamines and Anthrylamines via η3-Benzylpalladium Intermediates. Synlett, 2012, 23(17), 2431-2434.
8. Feng, X. J.; Sun, A. L.; Zhang, S.; Yu, X. Q.; Bao, M. Palladium-Catalyzed Carboxylative Coupling of Benzyl Chlorides with Allyltributylstannane: Remarkable Effect of Palladium Nanoparticles. Org. Lett. 2012, doi: 10.1021/ol303135e.
9. Wang, L. G.; Yu, X. Q.; Feng, X. J.; Bao, M., Synthesis of 3,5-Disubstituted Isoxazoles via Cope-Type Hydroamination of 1,3-Dialkynes. Org. Lett., 2012, 14(9), 2418–2421.
10. Xu, Z. W.; Yu, X. Q.; Feng, X. J.; Bao, M., Oxidative Coupling of Indoles with Ethyl 2-(Disubstituted Amino)Acetates: An Approach to Achieve Indolylglycine Derivatives. J. Org. Chem., 2012, 77(16), 7114–7118.
11. Feng, X. J.; Qu, Y. P.; Han, Y. L.; Yu, X. Q.; Bao, M.; Yamamoto, Y., Copper-catalyzed conversion of aryl and heteroaryl bromides into the corresponding chlorides. Chem. Commun., 2012,48(76), 9468-9470.
12. Yan, M.; Jin, T. N.; Ishikawa, Y.; Minato, T.; Fujita, T.; Chen, L. Y.; Bao, M.; Asao, N.; Chen, M. W.; Yamamoto, Y. Nanoporous gold catalyst for highly selective semihydrogenation of alkynes: remarkable effect of amine additives. J. Am. Chem. Soc., 2012, 134 (42), 17536–17542.
13. Zhang, S.; Wang, Y.; Feng, X.; Bao, M., Palladium-Catalyzed Amination of Chloromethylnaphthalene and Chloromethylanthracene Derivatives with Various Amines. J. Am. Chem. Soc. 2012, 134 (12), 5492–5495.
2011
1 .Yu, X.; Ma, Y.; Zhao, Z.; Xu, Z.; Bao, M., Cross-Coupling Reaction of Benzylic Halides with Allyltributylstannane Catalyzed by Cu(OTf)(2). Chin. J. Catal. 2011, 32, (3), 472-476.
2. Dai, Y.; Liu, H.; Feng, X.; Bao, M., Preparation and Application of New P, N-Ligands for Palladium-Catalyzed C-N Bond Coupling Reaction. Chin. J. Catal. 2011, 32, (10), 1617-1623.
3. Yang, F.; Jin, T.; Bao, M.; Yamamoto, Y., Facile synthesis of 3,4-diiododihydrothiophenes via electrophilic iodocyclization. Tetrahedron Lett. 2011, 52, (8), 936-938.
4. Feng, X. J.; Yan, M.; Zhang, X.; Bao, M., Preparation and application of SBA-15-supported palladium catalyst for Heck reaction in supercritical carbon dioxide. Chin. Chem. Lett. 2011, 22, (6), 643-646.
5. Yang, F.; Jin, T.; Bao, M.; Yamamoto, Y., Facile synthesis of diiodinated dihydronaphthalenes and naphthalenes via iodine mediated electrophilic cyclization. Chem. Commun. 2011, 47, (13), 4013-4015.
6. Yang, F.; Jin, T.; Bao, M.; Yamamoto, Y., Facile synthesis of 3,4-dihalofurans via electrophilic iodocyclization. Chem. Commun. 2011, 47, (15), 4541-4543.
7. Zhou, X.-Y.; Bao, M.; Zhou, Y.-G., Palladium-Catalyzed Asymmetric Hydrogenation of Simple Ketimines Using a Brønsted Acid as Activator. Adv. Synth. Catal. 2011, 353, (1), 84-88.
8. Zhou, X.-Y.; Wang, D.-S.; Bao, M.; Zhou, Y.-G., Palladium-catalyzed asymmetric hydrogenation of simple ketones activated by Brønsted acids. Tetrahedron Lett. 2011, 52, (22), 2826-2829.
9. Feng, X.; Zhao, Z.; Yang, F.; Jin, T.; Ma, Y.; Bao, M., 1,3-Diynes synthesis by homo-coupling of terminal alkynes using a Pd(PPh3)4/Ag2O simple catalyst system. J. Organometall. Chem. 2011, 696, (7), 1479-1482.
10. Peng, B.; Zhang, S.; Yu, X.; Feng, X.; Bao, M., Nucleophilic Dearomatization of Chloromethyl Naphthalene Derivatives via η3-Benzylpalladium Intermediates: A New Strategy for Catalytic Dearomatization. Org. Lett. 2011, 13, (19), 5402-5405.
11. Xu, Z.; Yu, X.; Feng, X.; Bao, M., Propargylamine Synthesis by Copper-Catalyzed Oxidative Coupling of Alkynes and Tertiary Amine N-Oxides. J. Org. Chem. 2011, 76, (16), 6901-6905.
12. Dai, Y.; Feng, X.; Liu, H.; Jiang, H.; Bao, M., Synthesis of 2-Naphthols via Carbonylative Stille Coupling Reaction of 2-Bromobenzyl Bromides with Tributylallylstannane Followed by the Heck Reaction. J. Org. Chem. 2011, 76, (24), 10068-10077.
13. Lu, S.; Jin, T.; Kwon, E.; Bao, M.; Yamamoto, Y., Highly Efficient Cu(OAc)2-Catalyzed Dimerization of Monofunctionalized Hydrofullerenes Leading to Single-Bonded [60]Fullerene Dimers. Angew. Chem. Int. Ed. 2011, 51, (3), 802-806.
14. Lu, S.; Jin, T.; Bao, M.; Yamamoto, Y., Cobalt-Catalyzed Hydroalkylation of [60]Fullerene with Active Alkyl Bromides: Selective Synthesis of Monoalkylated Fullerenes.J. Am. Chem. Soc. 2011, 133, (32), 12842-12848.
Published before2010
14.Peng, B.; Feng, X.; Zhang, X.; Ji, L.; Bao, M., Regioselective control using a catalyst switch in the reaction of diarylmethyl chlorides with allyltributylstannane. Tetrahedron 2010, 66, (32), 6013-6018.
13.Liu, Y.; Feng, X. J.; Bao, D. C.; Li, K. X.; Bao, M., Preparation of microcapsule-supported palladium catalyst using SPG (Shirasu Porous Glass) emulsification technique. Chin. Chem. Lett. 2010, 21, (8), 979-982.
12.Du, X.; Feng, X. J.; Liu, Y.; He, R.; Bao, M., Suzuki reaction of bromoallenes with arylboronic acids using an air-stable palladium complex Pd(Ph2PCH2CO2)2 as a precatalyst. Chin. Chem. Lett. 2010, 21, (6), 641-645.
11.Liu, Y.; Feng, X.; Bao, D.; Li, K.; Bao, M., A new method for the preparation of microcapsule-supported palladium catalyst for Suzuki coupling reaction. J. Mol. Catal. A: Chem. 2010, 323, (1-2), 16-22.
10.Peng, B.; Feng, X.; Zhang, X.; Zhang, S.; Bao, M., Propargylic and Allenic Carbocycle Synthesis through Palladium-Catalyzed Dearomatization Reaction. J. Org. Chem. 2010, 75, (8), 2619-2627.
9.Lu, S.; Jin, T.; Bao, M.; Yamamoto, Y., Palladium-Catalyzed Three-Component [3 + 2] Cycloaddition of Propargyl Trifluoroacetates, Ethylidene Malononitriles, and Allyltributylstannane. Org. Lett. 2010, 12, (4), 864-866.
8.Feng, X.; Yan, M.; Zhang, T.; Liu, Y.; Bao, M., Preparation and application of SBA-15-supported palladium catalyst for Suzuki reaction in supercritical carbon dioxide. Green Chem. 2010, 12, (10), 1758-1766.
7.Zhou, L.; Du, X.; He, R.; Ci, Z.; Bao, M., Nickel salt-catalyzed addition reaction of arylboronic acids to aromatic aldehydes. Tetrahedron Lett. 2009, 50, (4), 406-408.
6.Zhou, L. I.; Feng, X.; He, R.; Bao, M., X-ray structure of trans-chloro(1-naphthyl) bis(triphenylphosphine)nickel(II) and its application for catalytic dehalogenation of aryl chlorides. J. Coord. Chem. 2009, 62, (17), 2824-2831.
5.Du, X.; Dai, Y.; He, R.; Lu, S.; Bao, M., New Application of N-Halosuccinimide/PPh3 for the Halogenation of Propargyl Alcohols to Haloallenes. Synth. Commun. 2009, 39, (21), 3940-3949.
4.Lu, S.; Xu, Z.; Bao, M.; Yamamoto, Y., Carbocycle Synthesis through Facile and Efficient Palladium-Catalyzed Allylative De-aromatization of Naphthalene and Phenanthrene Allyl Chlorides. Angew. Chem. Int. Ed. 2008, 47, (23), 4366-4369.
3.Zhou, L.; Miao, Q.; He, R.; Feng, X.; Bao, M., Ni-catalyzed cross-coupling reaction of aryl chlorides with arylboronic acids in IPA without using a reducing reagent. Tetrahedron Lett. 2007, 48, (44), 7899-7902.
2.Zhang, T.; Feng, X.-J.; Wang, C.-X.; Bao, M., Cross-coupling reactions catalyzed by palladium in supercritical carbon dioxide. Chin. J. Org. Chem. 2007, 27, (12), 1463-1472.
1.Bao, M.; Hayashi, T.; Shimada, S., Cationic Organobismuth Complex with 5,6,7,12-Tetrahydrodibenz[c,f][1,5]azabismocine Framework and Its Coordination Complexes with Neutral Molecules. Organometallics 2007, 26, (7), 1816-1822.
2014Patents
ZL201210582568
ZL201110300963
ZL201110416062
ZL201110446150
ZL201210330796
ZL201210516382
2009-2013Patents
（2013）ZL201110165697
（2012）ZL200910010151
（2012）ZL200810228613
（2010）ZL200810012421
（2009）ZL200810010037
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