Pure and Applied Chemistry

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• Kajetanowicz Anna, Sytniczuk Adrian, Grela Karol: Metathesis of renewable raw materials—influence of ligands in the indenylidene type catalysts on self-metathesis of methyl oleate and cross-metathesis of methyl oleate with (Z)-2-butene-1,4-diol diacetate. Green Chem. 2014, 16, 1579. <http://dx.doi.org/10.1039/c3gc42194e>
• Yun Jeong In, Kim Hyoung Rae, Kim Sang Kyum, Kim Deukjoon, Lee Jongkook: Cross-metathesis of allyl halides with olefins bearing amide and ester groups. Tetrahedron 2012, 68, 1177. <http://dx.doi.org/10.1016/j.tet.2011.11.064>
• Barile Fabio, Bassetti Mauro, D'Annibale Andrea, Gerometta Renzo, Palazzi Michele: Cross-Metathesis Reactions of Homoallyl Methyl Malonates with Sterically Hindered Allylic Esters. Eur J Org 2011, 2011, 6519. <http://dx.doi.org/10.1002/ejoc.201100916>
• Yun Jeong In, Kim Deukjoon, Lee Jongkook: Cross-metathesis of allyl halides with olefins bearing an α-alkoxy amide group. Tetrahetron Lett 2011, 52, 1928. <http://dx.doi.org/10.1016/j.tetlet.2011.02.043>
• Loiseau François, Kholod Inga, Neier Reinhard: Thione Esters as Substrates for the Stereoselective Alkylation of Model Compounds of Nonactic Acids. Eur J Org Chem 2010, 2010, 4642. <http://dx.doi.org/10.1002/ejoc.200901513>
• Aljarilla Ana, López J. Cristóbal, Plumet Joaquín: Metathesis Reactions of Carbohydrates: Recent Highlights in Cross-Metathesis. Eur J Org Chem 2010, 2010, 6123. <http://dx.doi.org/10.1002/ejoc.201000570>
• Lin Yuya A., Chalker Justin M., Davis Benjamin G.: Olefin Cross-Metathesis on Proteins: Investigation of Allylic Chalcogen Effects and Guiding Principles in Metathesis Partner Selection. J Am Chem Soc 2010, 132, 16805. <http://dx.doi.org/10.1021/ja104994d>
• Julian Lisa D., Hartwig John F.: Intramolecular Hydroamination of Unbiased and Functionalized Primary Aminoalkenes Catalyzed by a Rhodium Aminophosphine Complex. J Am Chem Soc 2010, 132, 13813. <http://dx.doi.org/10.1021/ja1052126>
• Chalker Justin M., Bernardes Gonçalo J. L., Lin Yuya A., Davis Benjamin G.: Chemical Modification of Proteins at Cysteine: Opportunities in Chemistry and Biology. Chem Asian J 2009, 4, 630. <http://dx.doi.org/10.1002/asia.200800427>
• Lin Yuya A., Chalker Justin M., Davis Benjamin G.: Olefin Metathesis for Site-Selective Protein Modification. Chem Eur J of Chem Bio 2009, 10, 959. <http://dx.doi.org/10.1002/cbic.200900002>
• Yakushiji Fumika, Maddaluno Jacques, Yoshida Masahiro, Shishido Kozo: Diastereoselective construction of substituted tetrahydropyrans using an intramolecular oxy-Michael strategy. Tetrahetron Lett 2009, 50, 1504. <http://dx.doi.org/10.1016/j.tetlet.2009.01.084>
• Balof Shawna L., P'Pool Steven J., Berger Nancy J., Valente Edward J., Shiller Alan M., Schanz Hans-Jörg: Olefin metathesis catalysts bearing a pH-responsive NHC ligand: a feasible approach to catalyst separation from RCM products. Dalton Trans 2008, 5791. <http://dx.doi.org/10.1039/b809793c>
• Compain Philippe: Olefin Metathesis of Amine-Containing Systems: Beyond the Current Consensus. Adv Synth Catal 2007, 349, 1829. <http://dx.doi.org/10.1002/adsc.200700161>
• Kanada Regina M., Itoh Daisuke, Nagai Mitsuo, Niijima Jun, Asai Naoki, Mizui Yoshiharu, Abe Shinya, Kotake Yoshihiko: Total Synthesis of the Potent Antitumor Macrolides Pladienolide B and D. Angew Chem 2007, 119, 4428. <http://dx.doi.org/10.1002/ange.200604997>
• Kanada Regina M., Itoh Daisuke, Nagai Mitsuo, Niijima Jun, Asai Naoki, Mizui Yoshiharu, Abe Shinya, Kotake Yoshihiko: Total Synthesis of the Potent Antitumor Macrolides Pladienolide B and D. Angew Chem Int Ed 2007, 46, 4350. <http://dx.doi.org/10.1002/anie.200604997>
• Dunne Katherine S., Lee Sarah E., Gouverneur Véronique: Homometathesis and cross-metathesis coupling of phosphine-borane templates with electron-rich and electron-poor olefins. J Organomet Chem 2006, 691, 5246. <http://dx.doi.org/10.1016/j.jorganchem.2006.08.084>
• Boezio Alessandro A., Jarvo Elizabeth R., Lawrence Brian M., Jacobsen Eric N.: Efficient Total Syntheses of (−)-Colombiasin A and (−)-Elisapterosin B: Application of the Cr-Catalyzed Asymmetric Quinone Diels-Alder Reaction. Angew Chem 2005, 117, 6200. <http://dx.doi.org/10.1002/ange.200502178>
• Boezio Alessandro A., Jarvo Elizabeth R., Lawrence Brian M., Jacobsen Eric N.: Efficient Total Syntheses of (−)-Colombiasin A and (−)-Elisapterosin B: Application of the Cr-Catalyzed Asymmetric Quinone Diels-Alder Reaction. Angew Chem Int Ed 2005, 44, 6046. <http://dx.doi.org/10.1002/anie.200502178>
• Ferré-Filmon Karine, Delaude Lionel, Demonceau Albert, Noels Alfred F.: Stereoselective Synthesis of (E)-Hydroxystilbenoids by Ruthenium-Catalyzed Cross-Metathesis. Eur J Org Chem 2005, 2005, 3319. <http://dx.doi.org/10.1002/ejoc.200500068>
• Reynolds Nathan T., Rovis Tomislav: The effect of pre-existing stereocenters in the intramolecular asymmetric Stetter reaction. Tetrahedron 2005, 61, 6368. <http://dx.doi.org/10.1016/j.tet.2005.03.121>
• Chikkanna Dinesh, Singh Om V., Kong Suk Bin, Han Hyunsoo: A general asymmetric route for the synthesis of the alexine and australine family of pyrrolizidine alkaloids. The first asymmetric synthesis of 1,2-diepi-alexine and 1,2,7-triepi-australine. Tetrahetron Lett 2005, 46, 8865. <http://dx.doi.org/10.1016/j.tetlet.2005.10.074>
• Hoveyda Hamid R., Vézina Martin: Synthesis of Unsaturated Amino Alcohols through Unexpectedly Selective Ru-Catalyzed Cross-Metathesis Reactions^†. Org Lett 2005, 7, 2113. <http://dx.doi.org/10.1021/ol050387g>
• van Gerven Paul C. M., Elemans Johannes A. A. W., Gerritsen Jan W., Speller Sylvia, Nolte Roeland J. M., Rowan Alan E.: Dynamic combinatorial olefin metathesis: templated synthesis of porphyrin boxes. Chem Commun 2005, 3535. <http://dx.doi.org/10.1039/b503619d>
• Herndon James W: The chemistry of the carbon–transition metal double and triple bond: annual survey covering the year 2002. Coord Chem Rev - 2004, 248, 3. <http://dx.doi.org/10.1016/j.cct.2003.11.001>
• Grubbs Robert H.: Olefin metathesis. Tetrahedron 2004, 60, 7117. <http://dx.doi.org/10.1016/j.tet.2004.05.124>
• Singh Om V., Kampf Dorothy J., Han Hyunsoo: Oxazine formation by MsCl/Et3N as a convenient tool for the stereochemical interconversion of the hydroxyl group in N-acetyl 1,3-aminoalcohols. Asymmetric synthesis of N-acetyl l-xylo- and l-arabino-phytosphingosines. Tetrahetron Lett 2004, 45, 7239. <http://dx.doi.org/10.1016/j.tetlet.2004.08.030>
• Bisaro F., Gouverneur V.: Cross-metathesis, a versatile synthetic methodology for the construction of alkenyl phosphine oxides and bis-phosphine oxides. Tetrahetron Lett 2003, 44, 7133. <http://dx.doi.org/10.1016/S0040-4039(03)01842-2>
• Andreana Peter R., McLellan Jason S., Chen Yongchen, Wang Peng George: Synthesis of 2,6-Dideoxysugars via Ring-Closing Olefinic Metathesis. Org Lett 2002, 4, 3875. <http://dx.doi.org/10.1021/ol026710m>