Nitrogen Functionalization with <i>N</i>-(Fluorosulfonyl)carbamates

IF 0.2 4区 化学 Q4 CHEMISTRY, ORGANIC Journal of Synthetic Organic Chemistry Japan Pub Date : 2023-11-01 DOI:10.5059/yukigoseikyokaishi.81.1081
Takuya Hashimoto
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Abstract

Carbon-nitrogen bond formation with ammonia or its equivalent has been a major research field in organic chemistry since the discovery of Wöhler’s urea synthesis. Given the versatility of nitrogen-doped organic molecules in natural products, pharmaceuticals, agrochemicals and materials, many such transformations have been conceived during the last 200 years. While the focus has shifted more and more to developing new catalysts rather than reagents to achieve this goal, over the last couple of years we have been intrigued by the possibility of inventing new ammonia equivalents which suit modern catalytic synthesis. We review herein our recent study triggered by this renewed interest in reagent design, which has led to the discovery and application of N-(fluorosulfonyl)carbamates as a new class of aminating reagents.
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与<i>N</i>-(氟磺酰基)氨基甲酸酯的氮功能化
自发现Wöhler的尿素合成以来,与氨或其等价物形成碳氮键一直是有机化学的主要研究领域。考虑到氮掺杂有机分子在天然产品、药品、农用化学品和材料中的多功能性,在过去的200年里,人们设想了许多这样的转变。虽然焦点越来越多地转移到开发新的催化剂而不是试剂来实现这一目标,但在过去的几年里,我们对发明适合现代催化合成的新的氨当量的可能性很感兴趣。在此,我们回顾了最近在试剂设计方面的新兴趣所引发的研究,这导致了N-(氟磺酰基)氨基甲酸酯作为一类新的胺化试剂的发现和应用。
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来源期刊
CiteScore
0.30
自引率
0.00%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Information not localized
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