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Highly selective synthesis of functionalized polyhydroisoquinoline derivatives via a three-component domino reaction. X. Feng, J. J. Wang, Z. Xun, J. J. Zhang, Z. B. Huang, D. Q. Shi*, Chem. Commun., 2015, 51, 1528.
Multicomponent strategy to indeno[2,1-c]pyridine and hydroisoquinoline derivatives through cleavage of carbon-carbon bond. X. Feng, J. J. Wang, Z. Xun, Z. B. Huang, D. Q. Shi*, J. Org. Chem., 2015, 80, 1025.
Regioselective synthesis of functionalized [1,8]naphthyridine derivatives via a three-component domino reaction under catalyst-free conditions. X. Feng, J. J. Wang, J. J. Zhang, C. P. Cao, Z. B. Huang; D. Q. Shi*, Green Chem., 2015, 17, 973.
Highly efficient construction of a bridged pentacyclic skeleton via a six-component domino reaction under microwave irradiation. L. Fu, X. Feng, J. J. Zhang, J. D. Hu, Z. Xun, J. J. Wang, Z. B. Huang, D. Q. Shi*, Green Chem., 2015, 17, 1535.
Efficient Synthesis and Evaluation of Antitumor Activities of Novel Functionalized 1,8-Naphthyridines Derivatives. L. Fu, X. Feng, J. J. Wang, Z. Xun, J. D. Hu, J. J. Zhang, Y. W. Zhao, Z. B. Huang, D. Q. Shi*, ACS Comb. Sci., 2015, 17, 24.
Highly site-selective sequential alkenylation of oxalyl amide protected phenylpropylamine derivatives via a seven-membered palladacycle. Q. Wang, J. Han, C. Wang, J. Y. Zhang, Z. B. Huang, D. Q. Shi*, Y. S. Zhao*, Chem. Sci., 2014, 5, 4962.
Selective synthesis of polyfunctionalized pyrido[2,3-b]indoles by multicomponent domino reactions. J. D. Hu, C. P. Cao, W. Lin, M. H. Hu, Z. B. Huang*, D. Q. Shi*, J. Org. Chem., 2014, 79, 7935.
Oxalyl Amide Assisted Palladium-Catalyzed Arylation of C(sp2)-H Bond at the δ Position. J. Han, P. Liu, C. Wang, Q. Wang, J. Y. Zhang, Y. W. Zhao, D. Q. Shi, Z. B. Huang*, Y. S. Zhao*, Org. Lett., 2014, 16, 5682.
Fe-promoted oxidative cyclization of α-benzoylthioformanilides for the synthesis of 2-benzoyl- benzothiazoles. X. Feng, Q. Wang, Z. B. Huang, D. Q. Shi*, RSC Adv., 2014, 4, 54719.
Selective synthesis of polyfunctionalized hydroisoquinoline derivatives via a three-component domnio reaction. J. J. Zhang, J. D. Hu, C. P. Cao, G. L. Dou, L. Fu, Z. B. Huang, D. Q. Shi*, RSC Adv., 2014, 4, 62457.
Efficient Synthesis of Functionalized Benzo[b][1,8]naphthyridine Derivatives via Three-Component Reaction Catalyzed by L-Proline. L. Fu, W. Lin, M. H. Hu, X. C. Liu, Z. B. Huang*, D. Q. Shi*, ACS Comb. Sci., 2014, 16, 238.
Efficient and Regioselective Synthesis of Novel Functionalized Dispiropyrrolidines and Their Cytotoxic Activities. J. M. Yang, Y. Hu, Q. Li, F. Yu, J. Cao, D. Fang, Z. B. Huang, D. Q. Shi*, ACS Comb. Sci., 2014, 16, 139.
Selective reduction of carbonyl groups in the presence of low-valent titanium reagents. W. Lin, M. H. Hu, X. Feng, L. Fu, C. P. Cao, Z. B. Huang*, D. Q. Shi*, Tetrahedron Lett., 2014, 55, 2238.
An efficient three-component synthesis of highly functionalized tetrahydroacenaphtho[1,2-b]indolone derivatives catalyzed by L-proline. J. J. Zhang, X. Feng, X. C. Liu, Z. B. Huang, D. Q. Shi*, Mol. Divers., 2014, 18, 727.
Highly efficient construction of pentacyclic benzo[b]indeno[1,2,3-de][1,8]naphthyridine derivatives via four-component domino reaction. C. P. Cao, W. Lin, M. H. Hu, Z. B. Huang*, D. Q. Shi*, Chem. Commun., 2013, 49, 6983.
Highly efficient synthesis of polysubstituted pyrroles via four-component domino reaction. X. Feng, Q. Wang, W. Lin, G. L. Dou, Z. B. Huang*, D. Q. Shi*, Org. Lett., 2013, 15, 2542.
Facile, Efficient, and Diastereoselective Synthesis of Heterohelicene-like molecules. W. Lin, G. L. Dou, M. H. Hu, C. P. Cao, Z. B. Huang*, D. Q. Shi*, Org. Lett., 2013, 15, 1238.
GAP chemistry for pyrrolyl coumarin derivatives: a highly efficient one-pot synthesis under catalyst-free conditions. H. Y. Wang, X. C. Liu, X. Feng, Z. B. Huang*, D. Q. Shi*, Green Chem., 2013, 15, 3307.
Efficient Synthesis of Functionalized Dihydro-1H-indol-4(5H)-ones via One-Pot Three-Component Reaction Under Catalyst-Free Conditions. H. Y. Wang, D. Q. Shi*, ACS Comb. Sci., 2013, 15, 261.
An efficient and convenient synthesis of heterocycle-fused indazoles via the N-N bond forming reaction of nitroarenes induced by low-valent titanium reagent. W. Lin, M. H. Hu, X. Feng, C. P. Cao, Z. B. Huang*, D. Q. Shi*, Tetrahedron, 2013, 69, 6721.
An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by L-Proline. H. Y. Wang, L. L.Li, W. Lin, P. Xu, Z. B. Huang*, D. Q. Shi*, Org. Lett., 2012, 14, 4598.
Rapid and Efficient Ultrasound-Assisted Method for the Combinatorial Synthesis of Spiro[indoline-3,4”-pyrano[2,3-c] pyrazole] Derivatives. Y. Zou, Y. Hu, H. Liu, D. Q. Shi*, ACS Comb. Sci., 2012, 14, 38.
Novel and efficient synthesis of substituted quinoline-1-oxides and the complex compounds SnL2Cl2 (L = 2-aminoquinoline- 1-oxides) with the aid of stannous chloride. L. Fu, W. Lin, P. Xu, Y. K. Xi, M. M. Wang, D. Q. Shi*, Tetrahedron, 2012, 68, 7782.
A stereoselective synthesis of symmetrical and unsymmetrical bibenzo[e][1,3]oxazine-2,2’-dione derivatives induced by low- valent titanium reagent. G. L. Dou, F. Sun, D. Q. Shi*, Tetrahedron, 2012, 68, 4852.
An efficient synthesis of 2H-indazoles via reductive cyclization of 2-nitrobenzylamines induced by low-valent titanium reagent. F. Sun, X. Feng, X. Zhao, Z. B. Huang, D. Q. Shi*, Tetrahedron, 2012, 68, 3851.
A facile and efficient ultrasound-assisted synthesis of novel dispiroheterocycles through 1,3-dipolar cycloaddition reactions. Y. Hu, Y. Zou, H. Wu, D. Q. Shi*, Ultrason. Sonochem., 2012, 19, 264.
Efficient One-pot Three-Component Synthesis of Fused Pyridine Derivatives in Ionic Liquid. Z. B. Huang, Y. Hu, Y. Zhou, D. Q. Shi*, ACS Comb. Sci., 2011, 13, 45.
A novel and environment-friendly method for preparing dihydropyrano[2,3-c]pyrazoles in water under ultrasound irradiation. Y. Zhou, H. Wu, Y. Hu, H. Liu, X. Zhao, H. L. Ji, D. Q. Shi*, Ultrason. Sonochem., 2011, 18, 708.
An Efficient Synthesis of Pyrrolo[1,2-a]quinazolin-5(1H)-one Derivatives with the aid of Low-valent Titanium Reagent. G. L. Dou, D. Q. Shi*, Org. Biomol. Chem., 2011, 9, 7065.
Efficient one-pot synthesis of spiro[indoline-3,4'-pyrazolo [3,4-e][1,4]thiazepine]dione via three-component reaction. H. Chen, D. Q. Shi*, Tetrahedron, 2011, 67, 5686.
Efficient and convenient synthesis of spiroindoline- quinazolines induced by stannous chloride. Y. Hu, M. M. Wang, H. Chen, D. Q. Shi, Tetrahedron, 2011, 67, 9342.
An efficient one-step synthesis of 2-arylquinolin-4(3H)-ones with the aid of low-valent titanium reagent. F. Sun, X. Zhao, D. Q. Shi*, Tetrahedron Lett., 2011, 52, 5633.
A novel and convenient synthesis of 4-hydroxy-6-methyl-3-(1- (phenylimino)ethyl)-2H-pyran-2-one derivatives under ultrasound irradiation. H. Y. wang, Y. Zou, X. Zhao, D. Q. Shi*, Ultrason. Sonochem., 2011, 18, 1048.
Efficient synthesis of naphtho[1,2-e][1,3]oxazine derivatives via a chemoselective reaction with the aid of low-valent titanium reagent, D. Q. Shi*, S. F. Rong, G. L. Dou, M. M. Wang. J. Comb. Chem., 2010, 12, 25.
Oriented synthesis and in vitro anticancer activity of biquinazoline-2,2’-diones. G. L. Dou, D. Q. Shi*, Y. H. Li, J. Comb. Chem., 2010, 12, 195.
Efficient one-pot synthesis of spirooxindole derivatives catalyzed by L-proline in aqueous medium. Y. L. Li, H. Chen, C. L. Shi, D. Q. Shi*, S. J. Ji, J. Comb. Chem., 2010, 12, 231.
Regio- and stereoselective synthesis of novel dispiropyrrolidine bisoxindole derivatives via multicomponent reactions. H. Liu, G. L. Dou, D. Q. Shi*, J. Comb. Chem., 2010, 12, 292.
Regioselective Synthesis and in Vitro Anticancer Activity of 4-Aza-podophyllotoxin Derivatives Catalyzed by L-Proline. C. L. Shi, J. X. Wang, H. Chen, D. Q. Shi*, J. Comb. Chem., 2010, 12, 430.
Efficient One-Pot Synthesis of Novel Spirooxindole Derivatives via Three-Component Reaction in Aqueous Medium. H. Chen, D. Q. Shi*, J. Comb. Chem., 2010, 12, 571.
Efficient and Convenient Synthesis of Pyrrolo[1,2-a] quinazoline Derivatives with the Aid of Tin (II) Chloride. M. M. Wang, G. L. Dou, D. Q. Shi*, J. Comb. Chem., 2010, 12, 582.
Regioselective Synthesis of Novel Spiropyrrolidines and Spirothiapyrrolizidines Through Mnlticomponent 1,3-Dipolar Cycloaddition Reaction of Azomethin Ylides. H. Liu, G. L. Dou, D. Q. Shi*, J. Comb. Chem., 2010, 12, 633.