SYNTHESIS OF TRANS-2,6-PIPERIDINEDICARBOXAMIDE USING THE UGI REACTION. A PLAUSIBLE MODEL FOR THE BIOSYNTHESIS OF HALICHONADIN P

Mimura Rika; Kitamori Ayumi; Nakano Keiji; Kotsuki Hiyoshizo; Matsumoto Kenji; Kaneno Daisuke; Masuda Toshiya; Ichikawa Yoshiyasu

首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESIS OF TRANS-2,6-PIPERIDINEDICARBOXAMIDE USING THE UGI REACTION. A PLAUSIBLE MODEL FOR THE BIOSYNTHESIS OF HALICHONADIN P

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SYNTHESIS OF TRANS-2,6-PIPERIDINEDICARBOXAMIDE USING THE UGI REACTION. A PLAUSIBLE MODEL FOR THE BIOSYNTHESIS OF HALICHONADIN P

机译：使用UGI反应合成TRANS-2,6-哌啶二酰胺。拟南芥P生物合成的可能模型。

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The Ugi reaction of isocyanides, glutaraldehyde and glycine methyl ester is found to produce trans-2,6-piperidinedicarboxamides. It is proposed that this multi-component reaction is a plausible model for the biosynthesis of the marine natural product, halichonadin P.

机译：发现异氰酸酯，戊二醛和甘氨酸甲酯的Ugi反应可产生反式2,6-哌啶二甲酰胺。有人提出，这种多组分反应是海洋天然产物halichonadin P生物合成的合理模型。

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《Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry 》 |2016年第5期| 共9页
作者
Mimura Rika; Kitamori Ayumi; Nakano Keiji; Kotsuki Hiyoshizo; Matsumoto Kenji; Kaneno Daisuke; Masuda Toshiya; Ichikawa Yoshiyasu;
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1. SYNTHESIS OF TRANS-2,6-PIPERIDINEDICARBOXAMIDE USING THE UGI REACTION. A PLAUSIBLE MODEL FOR THE BIOSYNTHESIS OF HALICHONADIN P [J] . Mimura Rika, Kitamori Ayumi, Nakano Keiji, Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry . 2016 ,第5期

机译：使用UGI反应合成TRANS-2,6-哌啶二酰胺。拟南芥P生物合成的可能模型。
2. Bioinspired Synthesis of the Central Core of Halichonadin H: The Passerini Reaction in a Hypothetical Biosynthesis of Marine Natural Products [J] . Ichikawa Yoshiyasu, Yamasaki Toshiki, Nakanishi Keisuke, Synthesis: International Journal of Methods in Synthetic Organic Chemistry . 2019 ,第11期

机译：Bioinspired的Halichonadin H中央核心的合成：Passerini反应在海洋天然产物的假设生物合成中
3. Hormaomycin Analogues by Precursor-Directed Biosynthesis-Synthesis of and Feeding Experiments with Amino Acids Related to the Unique 3-(trans-2'-Nitrocyclopropyl)alanine Constituent [J] . Sergei I.Kozhushkov, Boris D.Zlatopolskiy, Melanie Brandl, European journal of organic chemistry . 2005 ,第5期

机译：前体定向生物合成的激素霉素类似物-与独特的3-（反式2'-硝基环丙基）丙氨酸成分相关的氨基酸的合成和进料实验
4. Biosynthesis of the Thiolactone Derivative of Enterococcus faecalis Gelatinase-Biosynthesis Activating Pheromone by using the Mycobacterium xenopi GyrA Mini-Intein [C] . Yosuke Yamanaka, Kou Hayakawa, Hidekazu Katayama Japanese peptide symposium . 2010

机译：肠球菌粪便蛋白甲状腺素衍生物的生物合成通过使用Xenopi Gyra Mini-Intein激活信息素激活信息素
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7. New Four-Component Ugi-Type Reaction. Synthesis of Heterocyclic Structures Containing a Pyrrolo1, 2-a1, 4diazepine Fragment [O] . -1

机译：新的四组分UGI型反应。合成含有吡咯的杂环结构1,2-a 1,4二氮杂普通片段的杂环结构

SYNTHESIS OF TRANS-2,6-PIPERIDINEDICARBOXAMIDE USING THE UGI REACTION. A PLAUSIBLE MODEL FOR THE BIOSYNTHESIS OF HALICHONADIN P

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