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J-GLOBAL ID：201602274927213957   Reference number：16A0713512

Catalytic asymmetric synthesis of the common amino acid component in the biosynthesis of tetrahydroisoquinoline alkaloids

テトラヒドロイソキノリンアルカロイド類の生合成における一般的アミノ酸成分の触媒性不斉合成

Author (8)： Tanifuji Ryo (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan) ,  Oguri Hiroki (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan) ,  Oguri Hiroki (Division of Applied Chemistry, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Nakacho, Koganei, Tokyo 184-8588, Japan) ,  Oguri Hiroki (Japan Science and Technology Agency (JST), PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan) ,  Koketsu Kento (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan) ,  Yoshinaga Yuki (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan) ,  Minami Atsushi (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan) ,  Oikawa Hideaki (Division of Chemistry, Graduate School of Science, Hokkaido University, North 10 West 8, Sapporo 060-0810, Japan)
Material： Tetrahedron Letters  (Tetrahedron Lett)
Volume： 57  Issue： 5  Page： 623-626  Publication year： Feb. 03, 2016 
JST Material Number： E0366A  ISSN： 0040-4039  Document type： Article
Article type： 短報  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： *isoquinoline alkaloid ,  biosynthesis ,  *amino acid ,  *asymmetric synthesis ,  precursor (substance) ,  *chemical reaction ,  Alkylation ,  metabolic pathway ,  catalytic reaction ,  synthetic intermediate ,  *Glycine Derivatives ,  *phase transfer reaction ,  Biosynthetic Pathways ,  amino acid biosynthesis ,  biosynthesis intermediate ,  phenolic compound ,  primary amine ,  organobromine compound ,  benzyl halide
Semi thesaurus term： *asymmetric synthetic reaction

Author keywords (4)： Tetrahydroisoquinoline alkaloid ,  Tyrosine derivative ,  Catalytic asymmetric synthesis ,  Common biosynthetic precursor

JST classification (4)： Amino acids  (CF10070V) ,  Alkaloids  (CF10030D) ,  Stereochemistry of organic reaction  (CF02130V) ,  Quinolines,isoquinolines  (CF07096H)

Substance index (6)： Tyrosine ,  Benzyl bromide ,  3-Hydroxy-O,5-dimethyl-L-tyrosine ,  (S)-2-Amino-3-(2,4-dimethoxy-3-methyl-5-hydroxyphenyl)propanoic acid ,  3-(Benzyloxy)-4-methoxy-5-methylbenzyl bromide ,  N-(Benzhydrylidene)glycine tert-butyl ester

Terms in the title (6)： テトラヒドロイソキノリン ,  アルカロイド類 ,  生合成 ,  アミノ酸 ,  触媒 ,  不斉合成