Recent Advances in Hypervalent Iodine Chemistry, Y.-N. Duan, S. Jiang, Y.-C. Han, B. Sun, C. Zhang *, Chin. J. Org. Chem. 2016, 36, 1973-1984.
Practical peptide synthesis mediated by a recyclable hypervalent iodine reagent and tris(4-methoxyphenyl)phosphine, C. Zhang*, S.-S. Liu, B. Sun, J. Tian, Org. Lett. 2015, 17, 4106-4109.
Recyclable hypervalent-iodine-mediated dehydrogenative α,β′-bifunctionalization of β-keto esters under metal-free conditions, Y.-N. Duan, L.-Q. Cui, L.-H. Zuo, C. Zhang*, Chem. Eur. J. 2015, 21, 13052-13057.
Iodosodilactone as a recyclable oxidant for efficient oxidation of alcohols to carbonyl compounds, A. Song, C. Zhang*, Acta Chim. Sinica 2015, 73, 1002-1006.
Boron trifluoride etherate functioning as a fluorine source in an iodosobenzene-mediated intramolecular aminofluorination of homoallylic amines, J. Cui, Q. Jia, R.-Z. Feng, S.-S. Liu, T. He, C. Zhang*, Org. Lett. 2014, 16, 1442-1445.
Synthesis of oxazolidin-2-ones and imidazolidin-2-ones directly from 1,3-diols or 3-amino alcohols using iodobenzene dichloride and sodium azide, T. He, W.-C. Gao, W.-K. Wang, C. Zhang*, Adv. Synth. Catal. 2014, 356, 1113-1118.
Iodine-mediated intramolecular amination of ketones: the synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups, W.-C. Gao, S. Jiang, R.-L. Wang, C. Zhang*, Chem. Commun. 2013, 49, 4890-4892.
Practical oxazole synthesis mediated by iodine from α-bromoketones and benzylamine derivatives, W.-C. Gao, R.-L. Wang, C. Zhang*, Org. Biomol. Chem. 2013, 11, 7123-7128.
Recyclable hypervalent iodine(III) reagent iodosodilactone as an efficient coupling reagent for direct esterification, amidation, and peptide coupling, J. Tian, W.-C. Gao, D.-M. Zhou, C. Zhang*, Org. Lett. 2012, 14, 3020-3023.
A mild and efficient direct α-amination of β-dicarbonyl compounds using iodosobenzene and p-toluenesulfonamide catalyzed by perchlorate zinc hexahydrate, J. Yu, S.-S. Liu, J. Cui, X.-S. Hou, C. Zhang*, Org. Lett. 2012, 14, 832-835.
A dramatic solvent effect on one-pot synthesis of substituted ureas directly from primary alcohols using the combined reagent of iodobenzene dichloride and sodium azide in ethyl acetate, C. Zhang*, W.-K. Wang, T. He, Synthesis 2012, 44, 3006-3014.
A simple and effective synthesis of benzolactones and benzolactams by noncatalytic benzylic oxidation of cyclic benzylic ethers and N-protected cyclic benzylic amines with sodium chlorite as an oxidant, A.-R. Song, J. Yu, C. Zhang*, Synthesis 2012, 44, 2903-2909.
Design, synthesis, structure, and dehydrogenation reactivity of a water-soluble o-iodoxybenzoic acid derivative bearing a trimethylammonium group, L.-Q. Cui, Z.-L. Dong, K. Liu, C. Zhang*, Org. Lett. 2011, 13, 6488-6491.
Effective oxidation of benzylic and alkane C-H bonds catalyzed by sodium o-iodobenzenesulfonate with Oxone as a terminal oxidant under phase-transfer conditions, L.-Q. Cui, K. Liu, C. Zhang*, Org. Biomol. Chem. 2011, 9, 2258-2265.
Enantioselective α-tosyloxylation of ketones catalyzed by spirobiindane scaffold-based chiral iodoarenes, J. Yu, J. Cui, X.-S. Hou, S.-S. Liu, W.-C. Gao, S. Jiang, J. Tian, C. Zhang*, Tetrahedron: Asymmetry. 2011, 22, 2039-2055.
One-pot synthesis of symmetrical 1,3-diarylureas or substituted benzamides directly from benzylic primary alcohols and effective oxidation of secondary alcohols to ketones using phenyliodine diacetate in combination with sodium azide, X.-Q. Li, W.-K. Wang, Y.-X. Han, C. Zhang*, Adv. Synth. Catal. 2010, 352, 2588-2598.
Various α-oxygen functionalizations of β-dicarbonyl compounds mediated by the hypervalent iodine(III) reagent p-iodotoluene difluoride with different oxygen-containing nucleophiles, J. Yu, J. Tian, C. Zhang*, Adv. Synth. Catal. 2010, 352, 531-546.
A simple and effective method for α-hydroxylation of β-dicarbonyl compounds using Oxone as an oxidant without a catalyst, J. Yu, J. Cui, C. Zhang*, Eur. J. Org. Chem. 2010, 7020-7026.
One-pot synthesis of carbamoyl azides directly from primary alcohols and oxidation of secondary alcohols to ketones using iodobenzene dichloride in combination with sodium azide, X.-Q. Li, W.-K. Wang, C. Zhang*, Adv. Synth. Catal. 2009, 351, 2342-2350.
A safe, convenient and efficient one-pot synthesis of α-chloroketone acetals directly from ketones using iodobenzene dichloride, J. Yu, C. Zhang*, Synthesis 2009, 2324-2328.
An environmentally benign TEMPO-catalyzed efficient alcohol oxidation system with a recyclable hypervalent iodine(III) reagent and its facile preparation, X.-Q. Li, C. Zhang*, Synthesis 2009, 1163-1169.
