“Rhodium-catalyzed acyloxy migration of propargylic esters in cycloadditions, inspiration from the recent “gold rush”
Shu, X.-Z.; Shu, D.; Schienebeck, C. M.; Tang, W.* Chem. Soc. Rev.2012, 41, 7698-7711. link.
“Rhodium-Catalyzed Carbonylation of Cyclopropyl Substituted Propargyl Esters: A Tandem 1,3-Acyloxy Migration [5 + 1] Cycloaddition”
Shu, D.; Li, X.; Zhang, M.; Robichaux, P. J.; Guzei, I. A.; Tang, W.* J. Org. Chem.2012, 77, 6463-6472. link.
.”Synthesis of Functionalized Cyclohexenone Core of Welwitindolinones via Rhodium-Catalyzed [5 + 1] Cycloaddition”
Zhang, M.; Tang, W.* Org. Lett.2012, 14, 3756-3759. link.
“Stereoselective Preparation of Cyclobutanes with Four Different Substituents: Total Synthesis and Structural Revision of Pipercyclobutanamide A and Piperchabamide G.”
Liu, R.; Zhang, M.; Wyche, T. P.; Winston-McPherson, G. N.; Bugni, T. S.; Tang, W.* Angew. Chem. Int. Ed.2012, 51, 7503-7506. link.
Highlight in Nature Chemical Biologylink.
“Catalytic Enantioselective Halolactonization of Enynes and Alkenes”
Zhang, W.; Liu, N.; Schienebeck, C. M.; Decloux, K.; Zheng, S. Werness, J. B.; Tang, W.* Chem.-Euro. J.2012, 18, 7296-7305. link.
Highlight in Synfacts, 2012, issue 7, 0790 (doi:10.1055/s-0031-1289837).
“Rhodium-catalyzed Intra- and Intermolecular [5+2] Cycloaddi-tion of 3-Acyloxy-1,4-enyne and Alkyne with Concomitant 1,2-Acyloxy Migration”
Shu, X.-z; Li, X.; Shu, D.; Huang, S.; Schienebeck, C. M.; Zhou, X.; Robichaux, P. J.; Tang, W.* J. Am. Chem. Soc.2012, 134, 5211-5221. link.
“Rhodium-Catalyzed Carbonylation of 3-Acyloxy-1,4-enynes for the Synthesis of Cyclopentenones”
Li, X.; Huang, S.; Schienebeck, C. M.; Shu, D.; Tang, W.* Org. Lett.2012, 14, 1584-1587. link.
“Rhodium-catalyzed 1,3-Acyloxy Migration and Subsequent Intramolecular [4+2] Cycloaddition of Vinylallene and Unactivated Alkyne”
Huang, S.; Li, X.; Lin, C. L.; Guzei, I. A.; Tang, W.* Chem. Commun.2012, 48, 2204-2206. link.
“Discovery of histone deacetylase 8 selective inhibitors”
Tang, W.*; Luo, T.; Greenberg, E. F.; Bradner, J. E.; Schreiber, S. L.* Bioorg. Med. Chem. Lett.2011, 21, 2601-2605. link.
“Effect of Halogenation Reagents on Halocyclization and Overman Rearrangement of Allylic Trichloroacetimidates”
Liu, N.; Schienebeck, C. M.; Collier, M. D.; Tang, W.* Tetrahedron Lett.2011, 52 , 6217-6219. link.
“Rhodium-catalyzed Ring Expansion of Cyclopropanes to Seven-membered Rings by 1,5-C-C Bond Migration”
Li, X.; Zhang, M.; Shu, D.; Robichaux, P. J.; Huang, S.; Tang, W.* Angew. Chem. Int. Ed.2011, 50, 10421-10424. link
“Interception of a Rautenstrauch Intermediate by Alkynes for [5+2] Cycloaddition: Rhodium-Catalyzed Cycloisomerization of 3-Acyloxy-4-ene-1,9-diynes to Bicyclo[5.3.0]decatrienes”
Shu, X.-z.; Huang, S.; Shu, D.; Guzei, I. A.; Tang, W.* Angew. Chem. Int. Ed.2011, 50, 8153-8156. link. Highlighted as “hot paper”
“Stereoselective Total Synthesis of (-)-Kumausallene”
Werness, J. B.; Tang, W.* Org. Lett. 2011, 13, 3664-3666. link.
Highlight in Synfacts, 2011, issue 10, 1042 (doi:10.1055/s-0030-1261141).
“Intramolecular 1,4-Addition of Nitrogen Nucleophile and Bromine Electrophile to Conjugated 1,3-Enyne”
Liu, N.; Werness, J. B.; Guzei, I. A. Tang, W.* Tetrahedron 2011, 67, 4385-4390. link
(Invited contribution for F. Dean Toste’s’ Tetrahedron Young Investigator Award.)
“Synthesis of Highly Functionalized Cyclohexenone Rings: Rhodium-Catalyzed 1,3-Acyloxy Migration and Subsequent [5+1] Cycloaddition”
Shu, D.; Li, X.; Zhang, M.; Robichaux, P. J.; Tang, W.* Angew. Chem. Int. Ed.2011, 50, 1346-1349. link.
“Synthesis of bromoallenyl pyrrolidines via 1,4-addition to 1,3-enynes”
Werness, J. B.; Tang, W.* Sci. China Chem.2011, 54, 56-60. link.
(Invited contribution for the 6th Sino-US Chemistry Professor Conference at Hangzhou, China.)
“Enantioselective Bromolactonization of Conjugated (Z)-Enynes”
Zhang, W.; Zheng, S.; Liu, N.; Werness, J. B.; Guzei, I. A.; Tang, W.* J. Am. Chem. Soc.2010, 132, 3664-3665. link.
Highlight in Angew. Chem. Int. Ed.link.
“Thermodynamic Control of the Electrocyclic Ring Opening of Cyclobutenes: C=X Substituents at C-3 Mask the Kinetic Torquoselectivity”
Um, J. M.; Xu, H.-D.; Houk, K. N.*; Tang, W.* J. Am. Chem. Soc.2009, 131, 6664-6665. link.
“DABCO-Catalyzed 1,4-Bromolactonization of Conjugated Enynes: Highly Stereoselective Formation of a StereogenicCenter and an Axially Chiral Allene”
Zhang, W.; Xu, H.-D.; Xu, H.; Tang, W.* J. Am. Chem. Soc.2009, 131, 3832-3833. link.
Highlight in Synfacts, 2009, issue 6, 0604 (doi:10.1055/s-0029-1216700).
“Intramolecular Hydroamination of Conjugated Enynes”
Zhang, W.; Werness, J. B.; Tang, W.* Tetrahedron 2009, 65, 3090-3095. link.
(Invited contribution for Justin DuBois’ Tetrahedron Young Investigator Award.)
“N,N’-(11S,12S)-(9,10-dihydro-9,10-ethanoanthracene-11,12-diyl)bis[2-(diphenylphosphino)-Benzamide”
Tang, W. The Encyclopedia of Reagents for Organic Synthesis [EROS], (Ed. P. L. Fuchs, John Wiley and Sons) 2008.
“Synthesis of Cyclobutenes by Highly Selective Transition-Metal-Catalyzed Ring Expansion of Cyclopropanes”
Xu, H.-D.; Zhang, W.; Shu, D.; Werness, J. B.; Tang, W.* Angew. Chem. Int. Ed.2008, 47, 8933-8936. link .
Highlight in Synfacts, 2009, issue 1, 0063 (doi:10.1055/s-0028-1087400).
“Base-Catalyzed Intramolecular Hydroamination of Conjugated Enynes”
Zhang, W.; Werness, J. B.; Tang, W.* Org. Lett.2008, 10, 2023-2026. link