钟为慧 - 浙江工业大学

研究领域

目前主要从事药物及中间体的绿色合成新方法、新技术工艺研究，Baylis-Hillman反应及其加成物在构建杂环化合物中的应用。

近期论文

查看导师新发文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

1．First construction of 12H-thiochromeno[2,3-b]quinolines and 5H-benzo[7,8]thiocino[2,3-b]quinolines via intramolecular Friedel-Crafts reaction of Morita-Baylis-Hillman adducts, Tetrahedron, 2011, in press. 2．New Procedure for the Preparation of (Z)-2-(5-Amino-1,2,4-thiadiazole-3-yl)- 2-trityloxyiminoacetic Acid, Organic Process Research & Development, 2011, in press. 3．First Application of Air-Stable and Reusable Phosphine Containing Calix[4]arene in Catalytic Aza-Baylis-Hillman Reaction, Synlett 2010, (20), 3057-3060. 4．Recent Advances in Construction of Nitrogen-containing Heterocycles from Baylis-Hillman Adducts，Org. Prep. Proced. Inter. 2011, 43(1), 1-66. 5．Stereoselective Chlorination of New Type Baylis-Hillman Adducts by bis(Trichloromethyl)carbonate with the Aide of Catalytic Amount of Triphenylphosphine Oxide, Lett. in Org. Chem. 2010, 7(3), 229-234. 6．A New Route to 5-Chloropyrazole-4-carbaldehydes and Their Reactivities in Baylis-Hillman Reaction, J. Chem. Res.(S), 2010, 370-374. 7．One-Pot Synthesis of New Type Aza-Baylis-Hillman Adducts from Chlorovinyl Aldehydes under Solvent-free Conditions, J. Chem. Res.(S) 2010, 44-49. 8．Efficient Synthesis of New Type Baylis-Hillman Adducts and Their Stereoselective Bromization, Synth. Commun., 2010, 40(16), 2441-2456. 9．An Efficient Synthesis of 4-Substituted Isoxazol-3-ols and Isoxazolidine-4-carbonitrile from Morita-Baylis-Hillman Bromides, Heterocycles, 2009, 12, 3053-3064. 10．A novel procedure for the synthesis of benzo[b][1,8]naphthyridine- -carboxylate derivatives from Morita-Baylis-Hillman adduct acetates, Synthesis, 2009, (14), 2333-2340. 11．Regioselective Synthesis of 5H-thiazolo[3,2-a]pyrimidin-5-ones from Baylis-Hillman Adducts under Solvent- and Base-Free Conditions, Synthesis, 2009, 1615-1622. 12．Efficient chemoselective addition of Grignard reagents to carbonyl compounds in 2-methyltetrahydrofuran, J. Chem. Res.(S) 2009, (6), 372-375. 13．An efficient synthesis of 3-arylmethyl-7,8-dihydro-6H-chromene-2,5-diones from Baylis-Hillman adduct acetates under solvent-free conditions, Tetrahedron, 2008, 64(23), 5491-5496； 14．A Convenient Synthesis of 2-(1H-1,2,4-Triazol-1-yl)-2H-1,4-benzothiazine Derivatives, Heteroatom Chemistry, 2008, 19(3), 332-336; 15．A novel access to 1,4-dichloroiso quinolines from phenacyl azides, Org. Prep. Pro. Inter. 2008, 40(6), 579-585. 16．Dramatically accelerated addition under solvent-free condition: an efficient synthesis of (E)-1,2,4-triazole substituted alkenes from Baylis-Hillman acetates, Synth. Commun. 2008, 38(19), 3291-3302; 17．An efficient Synthesis of 3-Arylmethyl-2-hydroxy- 7,8-dihydroquinolin-5(6H)-ones and 3-Arylmethyl-7,8- dihydroquinoline-2,5(1H,6H)-diones from Baylis-Hillman adduct acetates, Synthesis, 2008, (18), 2561-2568; 18．Cu(OAc)2 Catalyzed Cross-coupling of Pentafluorophenylboronic Acid with Amines under an Atmosphere of Oxygen, Synlett, 2008, 2888-2892; 19．Synthesis of Optically Active [Delta]-Dodecalactone via Chiral Resolution Using CPF, Synlett, 2007, 18(15), 2343-2346； 20．A method for the synthesis of 3a-aryl-substituted cyclopenta[1,2-b]furan derivatives, Synlett, 2005, (20), 3103-06；