炔丙醇

炔丙醇电还原自由基中间产物的ESR研究

An ESR Study of Radical Intermediates in Electroreduction of Propargyl Alcohol

此外有少量炔丙醇直接质子化生成部分饱和的烯丙醇。

Besides , a small amount of propargyl alcohol is directly protonated to allyl alcohol .

它们是许多天然产物和手性药物的重要中间体，例如甾体，维生素E，K等。手性炔丙醇类化合物的合成方法有多种多样。

Optically active propargyl alcohols can be used in diverse areas including the synthesis of many natural products and medicines . Such as steroids , vitamin E , K , etc. The preparation of chiral propinol are variety of methods .

氮杂环丙烷和芳基炔丙醇的串联开环关环反应

Tandem Ring-Opening / Closing Reactions of N-Ts Aziridines and Aryl Propargyl Alcohols

1,1-二取代炔丙醇氯代产物与4-甲基-7-羟基香豆素的异常缩合产物

Unusual Products from the Reaction of Chlorides of 1,1-Disubstituted Propargyl Alcohols with 4-Methyl-7-hydroxycoumarin

本论文的主要内容是对炔丙醇羧酸酯和氮杂环丙烷的反应性能进行系统的研究。

This dissertation mainly focused on the reactions of propargylic esters and aziridines .

官能团化手性炔丙醇的不对称合成研究及其在昆虫信息素不对称全合成中的应用

Asymmetric Synthesis of Functionalized Chiral Propargylic Alcohols and Application in Total Synthesis of Insect Pheromone

光学活性炔丙醇的合成

Synthesis of Optically Active Propargylic Alcohols

光学活性炔丙醇是合成许多药物、天然产物的重要前体物质。

Optically active propargyl alcohols are important and versatile building blocks for the synthesis of a wide range of Pharmaceuticals and natural products .

此章中我们主要介绍了通过强碱试剂、由强碱改进的有机试剂、末端炔烃衍生物和路易斯酸/碱组合等方法来合成炔丙醇。

This chapter mainly focused the synthesis of propargylic alcohols in many methods including strong base reagents and organic reagent improved by the strong base , the terminal alkyne , and Lewis acid or base .

有机高价碘在钯（Ⅱ）/铜（Ⅰ）共催化作用下与炔丙醇发生交叉偶联反应生成3取代炔丙醇。该反应不仅条件温和，产率很高，而且具有良好的区域选择性。

The Pd (ⅱ) / Cu (ⅰ) co catalyzed cross coupling reaction of propargyl alcohol with hypervalent iodonium salts to produce the 3 substituted propargyl alcohols in good to excellent yields under the mild conditions with high regioselectivity is discussed .

第一章主要是对炔丙基醇的合成方法做了简要的概述，炔丙醇通常是由末端炔烃对羰基化合物的加成反应合成。

The first chapter mainly introduces the methods for the preparation of propargylic alcohols using terminal alkynes and carbonyl compounds as starting materials .