Intramolecular cyclization of N-allyl propiolamides: a facile synthetic route to highly substituted γ-lactams (a review)

Intramolecular cyclization of N-allyl propiolamides: a facile synthetic route to highly substituted γ-lactams (a review)
复制标题

N-烯丙基丙炔酰胺的分子内环化:高度取代的 γ-内酰胺的简便合成路线(综述)

DOI:
10.1039/c7ra03075d
复制
发表时间:
2017
期刊:
影响因子:
3.9
通讯作者:
L. Edjlali
L. Edjlali
中科院分区:
化学3区
文献类型:
--
作者:
S. Soleimani‐Amiri;E. Vessally;M. Babazadeh;A. Hosseinian;L. Edjlali

文献摘要

参考文献

被引文献

相似文献

开发简单有效的方法来构建取代γ-内酰胺是一个重要的合成目标,因为这种环骨架存在于许多具有不同生物活性的天然化合物中。n -烯丙基丙酰胺分子内环化是合成上述化合物的一种高效、经济、操作简单的方法。在本综述中,我们将讨论用这些易于获取和用途广泛的构建块合成功能化γ-内酰胺衍生物的最新进展,重点讨论反应的机理方面。
The development of simple and efficient methods for construction of substituted γ-lactams is an important synthetic goal because such ring skeletons are present in numerous natural compounds that display diverse biological activities. Intramolecular cyclization of N-allyl propiolamides is an efficient, economic, and operationally simple strategy for the synthesis of the titled compounds. In the present review we will discuss recent advances in the synthesis of functionalized γ-lactam derivatives from these easily accessible and versatile building blocks with the emphasis on the mechanistic aspects of the reactions.
Codinaeopsin,一种抗疟疾真菌聚酮化合物。
DOI: 10.1021/ol801726k
发表时间: 2008-09-18
期刊: ORGANIC LETTERS
影响因子: 5.2
作者:
Kontnik, Renee;Clardy, Jon
通讯作者: Clardy, Jon
DOI: 10.1021/jm901098m
发表时间: 2009-10-08
影响因子: 7.3
作者:
Nett, Markus;Guider, Tobias A. M.;Kale, Andrew J.;Hughes, Chambers C.;Moore, Bradley S.
通讯作者: Moore, Bradley S.
DOI: 10.1016/j.ccr.2005.10.013
发表时间: 2005-11-01
期刊: CANCER CELL
影响因子: 50.3
作者:
Chauhan, D;Catley, L;Anderson, KC
通讯作者: Anderson, KC