Organic chemistry, Reagent, Stereochemistry, Organic synthesis and Trimethylsilyldiazomethane are his primary areas of study. He frequently studies issues relating to Methylation and Organic chemistry. His Reagent research is multidisciplinary, incorporating elements of Strecker amino acid synthesis, Nitrile, Phase, Combinatorial chemistry and Peptide synthesis.
He has researched Stereochemistry in several fields, including Cyclic peptide, Amino acid, Optically active and Stereoselectivity. His Organic synthesis study combines topics from a wide range of disciplines, such as Nuclear magnetic resonance spectroscopy, Aliphatic compound and Thiazole. Takayuki Shioiri usually deals with Trimethylsilyldiazomethane and limits it to topics linked to Diazomethane and Carboxylic acid.
His main research concerns Organic chemistry, Reagent, Stereochemistry, Organic synthesis and Trimethylsilyldiazomethane. His Synthon, Aliphatic compound, Ketone, Diazomethane and Aldol reaction investigations are all subjects of Organic chemistry research. The various areas that Takayuki Shioiri examines in his Reagent study include Combinatorial chemistry and Triethylamine.
Takayuki Shioiri combines subjects such as Amino acid, Cyclic peptide and Stereoselectivity with his study of Stereochemistry. His Stereoselectivity study incorporates themes from Moiety, Medicinal chemistry and Lactone. His study in Organic synthesis is interdisciplinary in nature, drawing from both Reaction conditions, Phosphorus, Wolff rearrangement and Acylation.
The scientist’s investigation covers issues in Stereochemistry, Organic chemistry, Total synthesis, Combinatorial chemistry and Trimethylsilyldiazomethane. His Stereochemistry research incorporates themes from Amino acid, Lyngbya majuscula, Cyclic peptide, Sponge and Stereoselectivity. His study in Organic chemistry concentrates on Cycloaddition, Benzofuran, Lignan, Diazo and Enantioselective synthesis.
His studies deal with areas such as Oxazole, Thiazole, Antillatoxin and Ceratospongamide as well as Total synthesis. Chemical synthesis, Aryl and Substituent is closely connected to Catalysis in his research, which is encompassed under the umbrella topic of Combinatorial chemistry. His research investigates the connection with Trimethylsilyldiazomethane and areas like Medicinal chemistry which intersect with concerns in Reaction conditions and Ammonium.
His primary scientific interests are in Stereochemistry, Organic chemistry, Total synthesis, Aldol reaction and Medicinal chemistry. His research on Stereochemistry focuses in particular on Lactone. His study on Organic chemistry is mostly dedicated to connecting different topics, such as Caprifoliaceae.
His work investigates the relationship between Total synthesis and topics such as Lyngbya majuscula that intersect with problems in Absolute configuration, Carboxylic acid, Enantioselective synthesis and Thiazoline. His work deals with themes such as Oxazole, Bromide, SN2 reaction, Combinatorial chemistry and Stereoselectivity, which intersect with Aldol reaction. His work in Medicinal chemistry tackles topics such as Trimethylsilyldiazomethane which are related to areas like Selectivity and Carbene.
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Diphenylphosphoryl azide. A new convenient reagent for a modified Curtus reaction and for the peptide synthesis.
Takayuki Shioiri;Kunihiro Ninomiya;Shunichi Yamada.
Journal of the American Chemical Society (1972)
Nicotianamine chelates both FeIII and FeII. Implications for metal transport in plants
Nicolaus von Wirén;Sukhbinder Klair;Suhkibar Bansal;Jean-Francois Briat.
Plant Physiology (1999)
New Methods and Reagents in Organic Synthesis. 14. A Simple Efficient Preparation of Methyl Esters with Trimethylsilyldiazomethane (TMSCHN2) and Its Application to Gas Chromatographic Analysis of Fatty Acids
N. Hashimoto;T. Aoyama;T. Shioiri.
Chemical & Pharmaceutical Bulletin (1981)
Cloning two genes for nicotianamine aminotransferase, a critical enzyme in iron acquisition (Strategy II) in graminaceous plants.
Michiko Takahashi;Hirotaka Yamaguchi;Hiromi Nakanishi;Takayuki Shioiri.
Plant Physiology (1999)
New methods and reagents in organic synthesis. 67. A general synthesis of derivatives of optically pure 2-(1-aminoalkyl)thiazole-4-carboxylic acids
Yasumasa Hamada;Makoto Shibata;Tsuneyuki Sugiura;Shinji Kato.
Journal of Organic Chemistry (1987)
New methods and reagents in organic synthesis. 75. asymmetric synthesis of α-hydroxy ketones using chiral phase transfer catalysts
Moriyasu Masui;Akira Ando;Takayuki Shioiri.
Tetrahedron Letters (1988)
New methods and reagents in organic synthesis. 51. A synthesis of ascidiacyclamide, a cytotoxic cyclic peptide from ascidian — determination of its absolute configuration
Yasumasa Hamada;Shinji Kato;Takayuki Shioiri.
Tetrahedron Letters (1985)
Diethyl phosphorocyanidated (DEPC). A novel reagent for the classical Strecker's α-amino nitrile synthesis☆
Shinya Harusawa;Yasumasa Hamada;Takayuki Shioiri.
Tetrahedron Letters (1979)
Efficient total synthesis of didemnins A and B
Yasumasa Hamada;Yutaka Kondo;Makoto Shibata;Takayuki Shioiri.
Journal of the American Chemical Society (1989)
Efficient total synthesis of AI-77-B, A gastroprotective substance from bacillus pumilus AI-77
Yasumasa Hamada;Osamu Hara;Akiyoshi Kawai;Yasushi Kohno.
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