Pure and Applied Chemistry

CrossRef Cited-by Linking

• Wang Chuan, Yamamoto Hisashi: Tungsten-Catalyzed Asymmetric Epoxidation of Allylic and Homoallylic Alcohols with Hydrogen Peroxide. J. Am. Chem. Soc. 2014, 136, 1222. <http://dx.doi.org/10.1021/ja411379e>
• Berkessel Albrecht, Günther Thomas, Wang Qifang, Neudörfl Jörg-M.: Titan-Salalen-Katalysatoren mit cis -1,2-Diaminocyclohexan-Rückgrat: enantioselektive Epoxidierung terminaler Olefine mit H 2 O 2. Angew. Chem. 2013, 125, 8625. <http://dx.doi.org/10.1002/ange.201210198>
• Berkessel Albrecht, Günther Thomas, Wang Qifang, Neudörfl Jörg-M.: Titanium Salalen Catalysts Based on cis -1,2-Diaminocyclohexane: Enantioselective Epoxidation of Terminal Non-Conjugated Olefins with H 2 O 2. Angew. Chem. Int. Ed. 2013, 52, 8467. <http://dx.doi.org/10.1002/anie.201210198>
• Infante Rebeca, Hernández Yulan, Nieto Javier, Andrés Celia: Enantioselective One-Pot Catalytic Synthesis of 4,5-Epoxy-3-alkanols and 1-Phenyl-2,3-epoxy-1-alkanols from α,β-Unsaturated Aldehydes. Eur. J. Org. Chem. 2013, 2013, 4863. <http://dx.doi.org/10.1002/ejoc.201300397>
• Srour Hassan, Le Maux Paul, Chevance Soizic, Simonneaux Gérard: Metal-catalyzed asymmetric sulfoxidation, epoxidation and hydroxylation by hydrogen peroxide. Coordination Chemistry Reviews 2013, 257, 3030. <http://dx.doi.org/10.1016/j.ccr.2013.05.010>
• Olivares-Romero José Luis, Li Zhi, Yamamoto Hisashi: Catalytic Enantioselective Epoxidation of Tertiary Allylic and Homoallylic Alcohols. J. Am. Chem. Soc. 2013, 135, 3411. <http://dx.doi.org/10.1021/ja401182a>
• Illa Ona, Namutebi Mariam, Saha Chandreyee, Ostovar Mehrnoosh, Chen C. Chun, Haddow Mairi F., Nocquet-Thibault Sophie, Lusi Matteo, McGarrigle Eoghan M., Aggarwal Varinder K.: Practical and Highly Selective Sulfur Ylide-Mediated Asymmetric Epoxidations and Aziridinations Using a Cheap and Readily Available Chiral Sulfide: Extensive Studies To Map Out Scope, Limitations, and Rationalization of Diastereo- and Enantioselectivities. J. Am. Chem. Soc. 2013, 135, 11951. <http://dx.doi.org/10.1021/ja405073w>
• Saisaha Pattama, de Boer Johannes W., Browne Wesley R.: Mechanisms in manganese catalysed oxidation of alkenes with H2O2. Chem. Soc. Rev. 2013, 42, 2059. <http://dx.doi.org/10.1039/c2cs35443h>
• Silva Eduarda M. P., Pye Richard J., Brown Geoffrey D., Harwood Laurence M.: Towards the Total Synthesis of Mycaperoxide B: Probing Biosynthetic Rationale. Eur J Org 2012, 2012, 1209. <http://dx.doi.org/10.1002/ejoc.201101477>
• Singh Rohit, Vince Robert: 2-Azabicyclo[2.2.1]hept-5-en-3-one: Chemical Profile of a Versatile Synthetic Building Block and its Impact on the Development of Therapeutics. Chem. Rev. 2012, 112, 4642. <http://dx.doi.org/10.1021/cr2004822>
• Pratt Russell C., Lyons Christopher T., Wasinger Erik C., Stack T. Daniel P.: Electrochemical and Spectroscopic Effects of Mixed Substituents in Bis(phenolate)–Copper(II) Galactose Oxidase Model Complexes. S J Am Chem Soc 2012, 134, 7367. <http://dx.doi.org/10.1021/ja211247f>
• Olivares-Romero José Luis, Li Zhi, Yamamoto Hisashi: Hf(IV)-Catalyzed Enantioselective Epoxidation of N-Alkenyl Sulfonamides and N-Tosyl Imines. S J Am Chem Soc 2012, 134, 5440. <http://dx.doi.org/10.1021/ja211880s>
• Yang Xia, Shen Kang, Liu Xuechao, Zhu Chengjian, Cheng Yixiang: Highly enantioselective fluorescent recognition of amino acid derivatives by unsymmetrical salan sensors. Tetrahetron Lett 2011, 52, 4611. <http://dx.doi.org/10.1016/j.tetlet.2011.06.084>
• Nishikawa Yasuhiro, Yamamoto Hisashi: Iron-Catalyzed Asymmetric Epoxidation of β,β-Disubstituted Enones. J Am Chem Soc 2011, 133, 8432. <http://dx.doi.org/10.1021/ja201873d>
• Gruner Konstanze K., Hopfmann Thomas, Matsumoto Kazuhiro, Jäger Anne, Katsuki Tsutomu, Knölker Hans-Joachim: Efficient iron-mediated approach to pyrano[3,2-a]carbazole alkaloids—first total syntheses of O-methylmurrayamine A and 7-methoxymurrayacine, first asymmetric synthesis and assignment of the absolute configuration of (−)-trans-dihydroxygirinimbine. Org Biomol Chem 2011, 9, 2057. <http://dx.doi.org/10.1039/c0ob01088j>
• Yang Xia, Liu Xuechao, Shen Kang, Fu Yong, Zhang Ming, Zhu Chengjian, Cheng Yixiang: Enantioselective fluorescent recognition of mandelic acid by unsymmetrical salalen and salan sensors. Biomol Chem 2011, 9, 6011. <http://dx.doi.org/10.1039/c1ob05361b>
• Adão Pedro, Avecilla Fernando, Bonchio Marcella, Carraro Mauro, Costa Pessoa João, Correia Isabel: Titanium(IV)-Salan Catalysts for Asymmetric Sulfoxidation with Hydrogen Peroxide. Eur J Inorg Chem 2010, 2010, 5568. <http://dx.doi.org/10.1002/ejic.201000792>
• Lv Chengwei, Wu Mei, Wang Shoufeng, Xia Chungu, Sun Wei: The synthesis of novel tetradentate ligands derived from salen and their application in enantioselective silylcyanation of aldehydes. Tet Asymm 2010, 21, 1869. <http://dx.doi.org/10.1016/j.tetasy.2010.05.050>
• Li Zhi, Yamamoto Hisashi: Zirconium(IV)- and Hafnium(IV)-Catalyzed Highly Enantioselective Epoxidation of Homoallylic and Bishomoallylic Alcohols. J Am Chem Soc 2010, 132, 7878. <http://dx.doi.org/10.1021/ja100951u>
• Lewis Simon E.: Synthetic methods : Part (ii) Oxidation and reduction methods. Annu Rep Prog Chem Sect B 2009, 105, 35. <http://dx.doi.org/10.1039/b822050f>
• Kuznetsov Maxim L., Pessoa João Costa: Epoxidation of olefins catalysed by vanadium–salan complexes: a theoretical mechanistic study. Dalton Trans 2009, 5460. <http://dx.doi.org/10.1039/b902424g>
• Matsumoto Kazuhiro, Sawada Yuji, Katsuki Tsutomu: ChemInform Abstract: Asymmetric Epoxidation of Olefins Catalyzed by Ti(salan) Complexes Using Aqueous Hydrogen Peroxide as the Oxidant. ChemInform 2008, 39. <http://dx.doi.org/10.1002/chin.200842258>