Pure and Applied Chemistry

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• Bai Yu, Tao Weijie, Ren Jun, Wang Zhongwen: Lewis Acid Catalyzed Intramolecular [4+2] and [3+2] Cross-Cycloaddition of Alkynylcyclopropane Ketones with Carbonyl Compounds and Imines. Angew. Chem. 2012, 124, 4188. <http://dx.doi.org/10.1002/ange.201200450>
• Bai Yu, Tao Weijie, Ren Jun, Wang Zhongwen: Lewis Acid Catalyzed Intramolecular [4+2] and [3+2] Cross-Cycloaddition of Alkynylcyclopropane Ketones with Carbonyl Compounds and Imines. Angew. Chem. Int. Ed. 2012, 51, 4112. <http://dx.doi.org/10.1002/anie.201200450>
• Xing Siyang, Pan Wenyan, Liu Chang, Ren Jun, Wang Zhongwen: Efficient Construction of Oxa- and Aza-[n.2.1] Skeletons: Lewis Acid Catalyzed Intramolecular [3+2] Cycloaddition of Cyclopropane 1,1-Diesters with Carbonyls and Imines. Angew Chem 2010, 122, 3283. <http://dx.doi.org/10.1002/ange.201000563>
• Xing Siyang, Pan Wenyan, Liu Chang, Ren Jun, Wang Zhongwen: Efficient Construction of Oxa- and Aza-[n.2.1] Skeletons: Lewis Acid Catalyzed Intramolecular [3+2] Cycloaddition of Cyclopropane 1,1-Diesters with Carbonyls and Imines. Angew Chem Int Ed 2010, 49, 3215. <http://dx.doi.org/10.1002/anie.201000563>
• LAUTENS M.: ChemInform Abstract: New Methods for the Control of Multiple Stereocenters. ChemInform 2010, 24, no. <http://dx.doi.org/10.1002/chin.199311329>
• Schindler Corinna S., Carreira Erick M.: Rapid formation of complexity in the total synthesis of natural products enabled by oxabicyclo[2.2.1]heptene building blocks. Chem Soc Rev 2009, 38, 3222. <http://dx.doi.org/10.1039/b915448p>
• Kuo Chun-Jung, Cheng Shu-Jin, Chang Shu-Ting, Liu Charng-Hsing: Palladium-Catalyzed 1,2-Addition of Organic Halides and Terminal Alkynes to 7-Oxabenzonorbornadiene: An Efficient Route to Polyaromatic Hydrocarbons. Eur J Org Chem 2008, 2008, 485. <http://dx.doi.org/10.1002/ejoc.200700772>
• Li Lih-Ping, Rayabarapu Dinesh Kumar, Nandi Malay, Cheng Chien-Hong: Asymmetric Reductive Ring-Opening of Bicyclic Olefins Catalyzed by Palladium and Nickel Complexes. Org Lett 2003, 5, 1621. <http://dx.doi.org/10.1021/ol034251z>
• López Fernando, Castedo Luis, Mascareñas José L.: A Practical Route to Enantiopure, Highly Functionalized Seven-Membered Carbocycles and Tetrahydrofurans: Concise Synthesis of (+)-Nemorensic Acid. Chem Eur J 2002, 8, 884. <http://dx.doi.org/10.1002/1521-3765(20020215)8:4<884::AID-CHEM884>3.0.CO;2-Q>
• Rayabarapu Dinesh Kumar, Chiou Chii-Feng, Cheng Chien-Hong: Highly Stereoselective Ring-Opening Addition of Terminal Acetylenes to Bicyclic Olefins Catalyzed by Nickel Complexes. Org Lett 2002, 4, 1679. <http://dx.doi.org/10.1021/ol025731d>
• Hunt Kevin W., Grieco Paul A.: Oxabicyclo[3.2.1]octenes in Organic SynthesisDirect Ring Opening of Oxabicyclo[3.2.1] Systems Employing Silyl Ketene Acetals in Concentrated Solutions of Lithium Perchlorate−Diethyl Ether:  Application to the Synthesis of the C(19)−C(27) Fragment of Rifamycin S. Org Lett 2001, 3, 481. <http://dx.doi.org/10.1021/ol0003836>
• López Fernando, Castedo Luis, Mascareñas José L.: Sulfinyl-Directed Diastereoselective [5 + 2] Pyrone−Alkene Cycloadditions:  A Practical Route to Enantiopure 8-Oxabicyclo[3.2.1]octane Derivatives. Org Lett 2000, 2, 1005. <http://dx.doi.org/10.1021/ol005724u>
• Ou Ligong, Hu Youhong, Song Guoqiang, Bai Donglu: Diastereoselective intramolecular [4+3] cycloaddition: Synthesis of a versatile precursor for preparation of 5,7-fused ring compounds. Tetrahedron 1999, 55, 13999. <http://dx.doi.org/10.1016/S0040-4020(99)00882-0>
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• Stohrer Ingo, Hoffmann H. Martin R.: Highly Diastereoselective Aldol Reaction of Bicyclo[3.2.1]oct-6-en-3-ones and 8-Oxabicyclo[3.2.1]oct-6-en-3-ones. (E)-Selective conversion into α-alkylidene ketones. HCA 1993, 76, 2194. <http://dx.doi.org/10.1002/hlca.19930760604>