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  1. Erlenmeyerkolben mit Weithals, Enghals, NS-Schliff oder Gewinde

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  1. Empress Wuyuan. Emperor Hui of Jin ( simplified Chinese: 晋惠帝; traditional Chinese: 晉惠帝; pinyin: Jìn Huì Dì; Wade–Giles: Chin Hui-ti; 259 – January 8, 307 [2] ), personal name Sima Zhong (司馬衷), courtesy name Zhengdu (正度), was the second emperor of the Jin dynasty (266–420). Emperor Hui was a developmentally ...

  2. 15. Sept. 2010 · The Erlenmeyer–Plöchl azlactone synthesis is the preparation of azlactones (also called oxazolones) in a Z configuration (originally assigned to the E configuration) by condensation of aromatic aldehydes with hippuric acid (the benzoyl glycine derivatives) in the presence of acetic anhydride. The azlactones are useful for the synthesis of α-ketos, a-amino acids and peptides. The ...

  3. Erlenmeyer–Plöchl吖内酯及氨基酸合成. Erlenmeyer–Plöchl吖内酯及氨基酸合成 (Erlenmeyer-Plöchl azlactone and amino acid synthesis). 将 甘氨酸 经过 噁唑酮 和 吖内酯 转变为其他 氨基酸 的过程。. [1] [2] 反应过程为:. 甘氨酸的苯甲酰衍生物 马尿酸 [3] 在 乙酸酐 存在下发生 ...

  4. 7. Aug. 2006 · The classical Erlenmeyer azlactone synthesis (1893) is an important method for preparing aromatic α-amino acids, 1 and azlactones continue to find diverse applications in synthesis as revealed by several recent reports. 2, 3, 4 These include asymmetric syntheses of various natural and unnatural amino acids 2, 3 and peptide synthesis. 4 The general revival of azlactone chemistry is exemplified ...

  5. 15. Sept. 2010 · The Erlenmeyer–Plöchl azlactone synthesis is the preparation of azlactones (also called oxazolones) in a Z configuration (originally assigned to the E configuration) by condensation of aromatic aldehydes with hippuric acid (the benzoyl glycine derivatives) in the presence of acetic anhydride. The azlactones are useful for the synthesis of α-ketos, a-amino acids and peptides. The ...

  6. 15. März 2007 · Click on the article title to read more.

  7. The Bergmann azlactone peptide synthesis is a classic organic synthesis process for the preparation of dipeptides . In the presence of a base, peptides are formed. s of N-carboxyanhydrides of amino acids with amino acid esters ( 1 ). [1] This reaction can be looked at in further detail by Bailey. [3]