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首页> 外文期刊>Angewandte Chemie >Stereoseleetive Syntheses of Peptide Derivatives with 2-Acetamido-3,4,6-tri-0-acetyl-i1amino-2-deoxy-β-D-glueopyr3nose by Four-Component Condensation
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Stereoseleetive Syntheses of Peptide Derivatives with 2-Acetamido-3,4,6-tri-0-acetyl-i1amino-2-deoxy-β-D-glueopyr3nose by Four-Component Condensation

机译:通过四组分缩合与2-乙酰氨基-3,4,6-三-0-乙酰基-i1氨基-2-脱氧-β-D-glueopyr3nose肽衍生物的立体异构合成

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摘要

Syntheses that feature the simultaneous reaction of several re-actants in a one-pot procedure are called multicomponent reactions (MCRs). In 1850 A. Sirecker discovered a reaction, subsequently named after him. which in our nomenclature is formulatedas S-3CR. and in which ammonia, carbonyl compounds, and hydrogen cyanide react to form α-aminoaikyl cyanides that can he bydroiyzed to the corresponding arnino acids. Since 1934 α-amino acids have been obtained by the Bucherer- Bergs reaction (BB-4CR),one of the very first 4CRs.
机译:以一锅法为特色的多种反应物同时反应的合成称为多组分反应(MCR)。 1850年,A。Sirecker发现了一种反应,后来以他的名字命名。我们将其命名为S-3CR。并且其中氨,羰基化合物和氰化氢反应形成α-氨基烷基氰化物,可以将其酰化为相应的阿尼诺酸。自1934年以来,通过最早的4CR之一的Bucherer-Bergs反应(BB-4CR)获得了α-氨基酸。

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