Name: Preparation and Reactions of Racemic and Optically Active Cyanohydrins (en Inglés)
Price: 98.77 USD
Availability: InStock
Author: Morsy Mohamed, Nesrin Mahmoud ; H. Mahran, Mohamed Refat ; A. Yosef, Hisham Abdallah
ISBN: 9786138829928

portada Preparation and Reactions of Racemic and Optically Active Cyanohydrins (en Inglés)

Preparation and Reactions of Racemic and Optically Active Cyanohydrins (en Inglés)

Formato

Libro Físico

Autor

Nesrin Mahmoud Morsy Mohamed

Mohamed Refat H. Mahran

Hisham Abdallah A. Yosef

Editorial

Scholars' Press

Idioma

Inglés

N° páginas

188

Encuadernación

Tapa Blanda

Dimensiones

22.9 x 15.2 x 1.1 cm

Peso

0.28 kg.

ISBN13

9786138829928

Categorías

Química orgánica

Preparation and Reactions of Racemic and Optically Active Cyanohydrins (en Inglés)

Nesrin Mahmoud Morsy Mohamed (Autor) · Mohamed Refat H. Mahran (Autor) · Hisham Abdallah A. Yosef (Autor) · Scholars' Press · Tapa Blanda

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Reseña del libro "Preparation and Reactions of Racemic and Optically Active Cyanohydrins (en Inglés)"

Chiral (R)-, (S)-cyanohydrins are widespread in nature in the form of the respective glycosides and serve roughly 3000 plants and many insects as antifeedants. For the preparative organic chemist, this class of compounds offers an enormous synthetic potential for making other chiral compounds accessible. In a few instances, the pharmacological principle of a drug also incorporates a chiral cyanohydrin as constitutive structural element. The development of simple synthetic procedures for cyanohydrins, which also entail a high degree of stereoselectivity, therefore has prime importance. In this respect, chiral cyanohydrins may serve as stereochemically pure starting materials Stereoselective follow-up of (R)-and (S)-cyanohydrins lead to other important classes of compounds with stereogenic centeres. Thus, starting from (R)-cyanohydrins, (R)-2-hydroxyaldehydes, (R)-2-hydroxyketones, (1R)-2-aminoalcohols and (1R, 2S)-2-aminoalcohols are easily obtained in high optical and chemical yields by appropriate transformations of the cyano-group.cyanohydrins can also produce optically active tertiary α-hydroxycarboxylic acid