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Recent Advances in the Synthesis of Acyl Fluorides
Synthesis ( IF 2.2 ) Pub Date : 2020-10-27 , DOI: 10.1055/s-0040-1705951
Marie Gonay , Chloé Batisse , Jean-François Paquin


Abstract

Acyl fluorides are valuable intermediates in organic synthesis. They are increasingly employed in peptide synthesis, in challenging esterification and amidation reactions or in transition-metal-catalyzed transformations. This review summarizes recent advances in their preparation.

1 Introduction

2 Nucleophilic Fluorination

2.1 α-Fluoroamine Reagents

2.2 Sulfur-Based Reagents

2.3 Metal Catalysts

2.4 Phosphorus-Based Reagents

2.5 N,N′-Dicyclohexylcarbodiimide/HF·Pyridine

2.6 Uranium Hexafluoride

2.7 Bromine Trifluoride

3 Radical Fluorination

4 Conclusion



Publication History

Received: 03 September 2020

Accepted: 28 September 2020

Publication Date:
27 October 2020 (online)

© 2020. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany



中文翻译:

酰基氟合成的最新进展


摘要

酰基氟是有机合成中有价值的中间体。它们越来越多地用于肽合成,具有挑战性的酯化和酰胺化反应或过渡金属催化的转化中。这篇综述总结了他们准备工作的最新进展。

1引言

2亲核氟化

2.1α-氟胺试剂

2.2硫基试剂

2.3金属催化剂

2.4磷基试剂

2.5 NN'-二环己基碳二亚胺/ HF·吡啶

2.6六氟化铀

2.7三氟化溴

3自由基氟化

4。结论



出版历史

收到:2020

年9月3日接受:2020年9月28日

发布日期:
2020年10月27日(在线)

©2020年。Thieme。版权所有

Georg Thieme Verlag
KGRüdigerstraße14,70469斯图加特,德国

更新日期:2020-10-30
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