THE FIRST SYNTHESIS OF PROTECTED 5-HYDROXYMETHYL-2-CYANOMETHYLBENZIMIDAZOLE

Isamu Katsuyama; Masanori Kubo

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THE FIRST SYNTHESIS OF PROTECTED 5-HYDROXYMETHYL-2-CYANOMETHYLBENZIMIDAZOLE

机译：保护的5-羟基甲基-2-氰基苄基咪唑的首次合成

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Protected 5-hydroxymethyl-2-cyanomethylbenzimidazole 4 has successfully been synthesized starting from 3,4-diaminobenzoic acid 1.The benzimidazole 4 is expected to be a useful intermediate for the synthesis of new functional molecules such as drugs,agrochemicals,dyes,perfumes,and cosmetics.

机译：受保护的5-羟甲基-2-氰基甲基苯并咪唑4已成功地从3,4-二氨基苯甲酸1开始合成。苯并咪唑4有望成为合成新功能分子的有用中间体，例如药物，农用化学品，染料，香料，和化妆品。

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《Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry》 |2007年第11期|共7页
作者
Isamu Katsuyama; Masanori Kubo;
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1. THE FIRST SYNTHESIS OF PROTECTED 5-HYDROXYMETHYL-2-CYANOMETHYLBENZIMIDAZOLE [J] . Isamu Katsuyama, Masanori Kubo Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry . 2007,第11期

机译：保护的5-羟基甲基-2-氰基苄基咪唑的首次合成
2. Synthesis of orthogonally protected enantiopure 2,9-diaminodecanedioic acid:a model for a new general method for the synthesis of orthogonally protected alpha,alpha'-diaminodicarboxylic acids [J] . Cyrille Truchot, N.Andre Sasaki Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry . 2004,第0期

机译：正交保护的对映纯2,9-二氨基癸二酸的合成：用于合成正交保护的α，α'-二氨基二羧酸的新通用方法的模型
3. Synthesis of HCV replicase inhibitors: Base-catalyzed synthesis of protected α-hydrazino esters and selective aerobic oxidation with catalytic Pt/Bi/C for synthesis of imidazole-4,5-dicarbaldehyde [J] . Bowman R.K., Brown A.D., Cobb J.H., The Journal of Organic Chemistry . 2013,第23期

机译：HCV复制酶抑制剂的合成：受保护的α-肼基酯的碱催化合成和Pt / Bi / C催化的选择性好氧氧化反应合成咪唑-4,5-二甲醛
4. THE USEFULNESS OF ORTHOGONAL PROTECTING GROUP STRATEGY: SYNTHESIS OF FOUR HEPARIN TETRASACCHARIDES FROM A SINGLE PROTECTED INTERMEDIATE [C] . Jakab Zs., Fugedi P. International Carbohydrate Symposium . 2013

机译：正交保护群体策略的有用性：来自单一保护中间体的四种肝素四糖的合成
5. Toward the total synthesis of a novel Pir protein ester linked glycopeptide by development of a new sugar O2-protecting group and a new solid phase peptide synthesis linker. [D] . Cai, Feng. 2009

机译：通过开发新的糖O2保护基和新的固相肽合成接头，可实现新的Pir蛋白酯连接的糖肽的总合成。
6. One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters [O] . Gastón Silveira-Dorta, Sergio J Álvarez-Méndez, Víctor S Martín, 2016

机译：从N保护的α-氨基酯一锅法合成对映体纯的N保护的烯丙基胺
7. Synthesis of Protected 3,4- and 2,3-Dimercaptophenylalanines as Building Blocks for Fmoc-Peptide Synthesis and Incorporation of the 3,4-Analogue in a Decapeptide Using Solid-Phase Synthesis [O] . -1

机译：合成保护3,4-和2,3-二巯基苯氨基氨酸作为用于FMOC-肽合成的结构块，并使用固相合成将3,4-类似物掺入3,4-类似物质

THE FIRST SYNTHESIS OF PROTECTED 5-HYDROXYMETHYL-2-CYANOMETHYLBENZIMIDAZOLE

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