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第36讲-α-反应性和缩合反应

Lecture 36 - α-Reactivity and Condensation Reactions
课程网址: http://videolectures.net/yalespan125bs2011_mcbride_lec36/  
主讲教师: J. Michael McBride
开课单位: 耶鲁大学
开课时间: 2014-08-19
课程语种: 英语
中文简介:
在许多合成过程中,酮烷基化的一个重要挑战是选择能够控制异构和单取代与多取代的试剂和条件。β-二羰基化合物允许方便的烷基化以及酮和羧酸的制备。羟醛缩合,其中α-位置加上羰基生成β-羟基或α,β-不饱和羰基化合物,可通过去除水来完成。罗宾逊环化反应是α,β-不饱和羰基化合物共轭加成反应的一个重要例子。在克莱森缩合反应中,酯的α-酰化是脂肪酸生物合成的关键步骤。确定糖的组成结构对早期的碳水化合物化学家提出了严峻的挑战。
课程简介: As in many synthetic procedures, an important challenge in ketone alkylation is choosing reagents and conditions that allow control of isomerism and of single vs. multiple substitution. β-Dicarbonyl compounds allow convenient alkylation and preparation of ketones and carboxylic acids. The aldol condensation, in which an α-position adds to a carbonyl group to generate a β-hydroxy- or an α,β-unsaturated carbonyl compound, can be driven to completion by removal of water. The Robinson annulation reaction is an important example of conjugate addition to α,β-unsaturated carbonyl compounds. α-Acylation of esters as in the Claisen condensation is a key step in the biosynthesis of fatty acids. Determining the constitutional structure of sugars posed a daunting challenge to early carbohydrate chemists.
关 键 词: 酮烷基化; 共轭加成反应; 缩合反应
课程来源: 视频讲座网
数据采集: 2021-11-18:zkj
最后编审: 2021-11-18:zkj
阅读次数: 90