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炔烃的催化氢胺化反应。

The catalytic hydroamination of alkynes.

作者信息

Pohlki Frauke, Doye Sven

机构信息

Institut für Organische Chemie, Universität Hannover, Schneiderberg 1B, D-30167 Hannover, Germany.

出版信息

Chem Soc Rev. 2003 Mar;32(2):104-14. doi: 10.1039/b200386b.

Abstract

The direct addition of ammonia or primary and secondary amines to non-activated alkenes and alkynes is potentially the most efficient approach towards the synthesis of higher substituted nitrogen-containing products. It represents the most atom economic process for the formation of amines, enamines and imines, which are important bulk and fine chemicals or building blocks in organic synthesis. While the hydroamination of alkenes is still limited to more or less activated alkenes, great progress has been achieved in the case of alkynes over the last three years. To illustrate this progress, the review will mostly focus on recent developments in the field of intermolecular hydroamination of alkynes. However, if it is necessary for the discussion, older results and intramolecular reactions, which can be achieved more easily, will be mentioned as well.

摘要

将氨或伯胺和仲胺直接加成到未活化的烯烃和炔烃上,可能是合成高取代含氮产物最有效的方法。它是形成胺、烯胺和亚胺最原子经济的过程,这些都是有机合成中重要的大宗和精细化学品或结构单元。虽然烯烃的氢胺化仍局限于或多或少被活化的烯烃,但在过去三年里,炔烃的氢胺化取得了很大进展。为了阐述这一进展,本综述将主要关注炔烃分子间氢胺化领域的最新发展。然而,如有必要进行讨论,也会提及较早的结果以及更容易实现的分子内反应。

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