Pure and Applied Chemistry

CrossRef Cited-by Linking

• Xiao Zijun, Lu Jian R.: Strategies for enhancing fermentative production of acetoin: A review. Biotechnology Advances 2014, 32, 492. <http://dx.doi.org/10.1016/j.biotechadv.2014.01.002>
• Ohfune Yasufumi, Oe Kentaro, Namba Kosuke, Shinada Tetsuro: Total Synthesis of Manzacidins. An Overview and Perspective. HETEROCYCLES 2012, 85, 2617. <http://dx.doi.org/10.3987/REV-12-746>
• Sacchetti Alessandro, Silvani Alessandra, Gatti Francesco G., Lesma Giordano, Pilati Tullio, Trucchi Beatrice: Addition of TMSCN to chiral ketimines derived from isatin. Synthesis of an oxindole-based peptidomimetic and a bioactive spirohydantoin. Biomol Chem 2011, 9, 5515. <http://dx.doi.org/10.1039/c1ob05532a>
• Aydillo Carlos, Avenoza Alberto, Busto Jesús H., Jiménez-Osés Gonzalo, Peregrina Jesús M., Zurbano María M.: α-Alkylation versus retro-O-Michael/γ-alkylation of bicyclic N,O-acetals: an entry to α-methylthreonine. Tet Asymm 2008, 19, 2829. <http://dx.doi.org/10.1016/j.tetasy.2008.11.031>
• Hashimoto Takuya, Maruoka Keiji: Syntheses of manzacidins: a stage for the demonstration of synthetic methodologies. Org Biomol Chem 2008, 6, 829. <http://dx.doi.org/10.1039/b716062c>
• Meyer Udo, Bisel Philippe, Weckert Edgar, Frahm August Wilhelm: Bicyclic glutamic acid derivatives. Chirality 2006, 18, 383. <http://dx.doi.org/10.1002/chir.20260>
• Vogt Henning, Baumann Thomas, Nieger Martin, Bräse Stefan: Direct Asymmetric α-Sulfamidation of α-Branched Aldehydes: A Novel Approach to Enamine Catalysis. Eur J Org Chem 2006, 2006, 5315. <http://dx.doi.org/10.1002/ejoc.200600587>
• Meyer Udo, Bisel Philippe, Bräuner-Osborne Hans, Madsen Ulf, Höfner Georg, Wanner Klaus Th., Frahm August Wilhelm: Rigid nonproteinogenic cyclic amino acids as ligands for glutamate receptors:trans-Tris(homoglutamic) acids. Chirality 2005, 17, 99. <http://dx.doi.org/10.1002/chir.20110>
• Ohfune Yasufumi, Shinada Tetsuro: Enantio- and Diastereoselective Construction of α,α-Disubstituted α-Amino Acids for the Synthesis of Biologically Active Compounds. Eur J Org Chem 2005, 2005, 5127. <http://dx.doi.org/10.1002/ejoc.200500434>
• Asymmetric Strecker Route toward the Synthesis of Biologically Active α,α-Disubstituted α-Amino Acids. Bull Chem Soc Jpn 2003, 76, 1115. <http://dx.doi.org/10.1246/bcsj.76.1115>
• Warmuth Ralf, Munsch Tamara E, Stalker Robert A, Li Bing, Beatty Alicia: Enantioselective synthesis of benzocyclic α,α-dialkyl-amino acids: new insight into the solvent dependent stereoselectivity of the TMSCN addition to phenylglycinol derived imines. Tetrahedron 2001, 57, 6383. <http://dx.doi.org/10.1016/S0040-4020(01)00505-1>
• Namba Kosuke, Kawasaki Masanori, Takada Ichinori, Iwama Seiji, Izumida Masashi, Shinada Tetsuro, Ohfune Yasufumi: Novel and efficient transformation of α-amino nitrile to α-imino and α-amide nitriles in asymmetric Strecker synthesis. Tetrahetron Lett 2001, 42, 3733. <http://dx.doi.org/10.1016/S0040-4039(01)00551-2>
• Béraud Valérie, Perfetti Patricia, Pfister Christine, Kaafarani Mustapha, Vanelle Patrice, Crozet Michel P.: Synthesis of Cαα-unsymmetrically disubstituted nitroesters by electron transfer C-alkylation of ethyl 2-nitropropionate anion. Tetrahedron 1998, 54, 4923. <http://dx.doi.org/10.1016/S0040-4020(98)00194-X>
• Wirth Thomas: Neue Strategien zu α-alkylierten α-Aminosäuren. Angew Chem 1997, 109, 235. <http://dx.doi.org/10.1002/ange.19971090306>
• Trost Barry M., Ariza Xavier: Katalytische asymmetrische Alkylierung von Nucleophilen - asymmetrische Synthese α-alkylierter Aminosäuren. Angew Chem 1997, 109, 2749. <http://dx.doi.org/10.1002/ange.19971092323>
• Zhou Changyou, Fang Zhiqiang, O'Donnell Martin J., Scott William L.: The solid phase synthesis of α,α-disubstituted unnatural amino acids and peptides (di-UPS). Tetrahetron Lett 1997, 38, 3695. <http://dx.doi.org/10.1016/S0040-4039(97)00715-6>