Metal‐Enabled Reactions of Nitrenes with Alkynes: Beyond Gold Catalysis. Issue 10 (8th March 2022)
- Record Type:
- Journal Article
- Title:
- Metal‐Enabled Reactions of Nitrenes with Alkynes: Beyond Gold Catalysis. Issue 10 (8th March 2022)
- Main Title:
- Metal‐Enabled Reactions of Nitrenes with Alkynes: Beyond Gold Catalysis
- Authors:
- Ren, Miaofeng
Wang, Yu‐Chao
Ren, Shangfeng
Huang, Keke
Liu, Jin‐Biao
Qiu, Guanyinsheng - Abstract:
- Abstract: As versatile synthons, nitrenes have attracted great attention. Two research topics, including nitrene precursor development and nitrene‐based transformations, have been thoroughly investigated so far. Generally, different nitrene precursors under various metal catalysis have allowed for the differentiation of the reactivity of the resulting nitrene, thus enabling diverse C−H insertions, aziridinations, and sulfimidations with high reaction efficiency and reaction generality. Among the addition of nitrenes with unsaturated bonds, the reaction of nitrenes and alkynes is still in its initial stage, although various metal‐catalyzed transformations, typically, rhodium‐catalyzed sulfinamate‐derived nitrene/alkyne metalation, have been well‐developed. Two types of plausible mechanism, radical and electrophilic models, have been proposed. The simple preparation of acyl nitrenes and their enantioselective reaction with alkynes, as well as their applications in biologically interesting architectures, is of great interest. In this review, we would like to describe the reaction of nitrenes with alkynes under metal catalysis. To increase readability, this review will be presented according to mechanistic pathways and types of metal. Abstract : Radical radicals : The facile generation of acyl nitrenes, their enantioselective reaction with alkynes and their applications in the preparation of biologically interesting architectures, remain significant targets. This review focusesAbstract: As versatile synthons, nitrenes have attracted great attention. Two research topics, including nitrene precursor development and nitrene‐based transformations, have been thoroughly investigated so far. Generally, different nitrene precursors under various metal catalysis have allowed for the differentiation of the reactivity of the resulting nitrene, thus enabling diverse C−H insertions, aziridinations, and sulfimidations with high reaction efficiency and reaction generality. Among the addition of nitrenes with unsaturated bonds, the reaction of nitrenes and alkynes is still in its initial stage, although various metal‐catalyzed transformations, typically, rhodium‐catalyzed sulfinamate‐derived nitrene/alkyne metalation, have been well‐developed. Two types of plausible mechanism, radical and electrophilic models, have been proposed. The simple preparation of acyl nitrenes and their enantioselective reaction with alkynes, as well as their applications in biologically interesting architectures, is of great interest. In this review, we would like to describe the reaction of nitrenes with alkynes under metal catalysis. To increase readability, this review will be presented according to mechanistic pathways and types of metal. Abstract : Radical radicals : The facile generation of acyl nitrenes, their enantioselective reaction with alkynes and their applications in the preparation of biologically interesting architectures, remain significant targets. This review focuses on the recent advances of the reaction of nitrenes with alkynes under metal catalysis according to the mechanistic pathway and type of transition metal employed. … (more)
- Is Part Of:
- ChemCatChem. Volume 14:Issue 10(2022)
- Journal:
- ChemCatChem
- Issue:
- Volume 14:Issue 10(2022)
- Issue Display:
- Volume 14, Issue 10 (2022)
- Year:
- 2022
- Volume:
- 14
- Issue:
- 10
- Issue Sort Value:
- 2022-0014-0010-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-03-08
- Subjects:
- Copper-catalyzed -- C−N bond -- green catalysis -- N-centered radicals
Catalysis -- Periodicals
541.39505 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1867-3899 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cctc.202200008 ↗
- Languages:
- English
- ISSNs:
- 1867-3880
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21560.xml