Chemical Communications, Год журнала: 2021, Номер 57(81), С. 10596 - 10599
Опубликована: Янв. 1, 2021
Reduction of primary and secondary amides to amines without the need any catalyst has been developed.
Язык: Английский
Chemical Communications, Год журнала: 2021, Номер 57(81), С. 10596 - 10599
Опубликована: Янв. 1, 2021
Reduction of primary and secondary amides to amines without the need any catalyst has been developed.
Язык: Английский
Chemical Reviews, Год журнала: 2021, Номер 121(20), С. 12784 - 12965
Опубликована: Авг. 27, 2021
This review serves to document advances in the synthesis, versatile bonding, and reactivity of molecular main group metal hydrides within Groups 1, 2, 12–16. Particular attention will be given emerging use said rapidly expanding field Main Group element-mediated catalysis. While this is comprehensive nature, focus research appearing open literature since 2001.
Язык: Английский
Процитировано
211Chemical Reviews, Год журнала: 2022, Номер 122(9), С. 8261 - 8312
Опубликована: Март 7, 2022
The addition of a B–H bond to an unsaturated (polarized or unpolarized) is powerful and atom-economic tool for the synthesis organoboranes. In recent years, s-block organometallics have appeared as alternative catalysts transition-metal complexes, which traditionally catalyze hydroboration bonds. Because rapid development in field bonds catalyzed by alkali (Li, Na, K) alkaline earth (Mg, Ca, Sr, Ba) metals, we provide detailed updated comprehensive review that covers synthesis, reactivity, application metal polarized well carbon–carbon Moreover, describe main reaction mechanisms, providing valuable insight into reactivity catalysts. Finally, compare these complexes with other redox-neutral catalytic systems based on p-block metals including aluminum f-block lanthanides early actinides. this review, aim comprehensive, authoritative, critical assessment state art within highly interesting research area.
Язык: Английский
Процитировано
112Advanced Synthesis & Catalysis, Год журнала: 2021, Номер 363(21), С. 4818 - 4840
Опубликована: Сен. 16, 2021
Abstract Hydroboration of alkynes is special interest to researchers since it the most straightforward process for synthesis highly important vinylborane synthetic intermediate compounds. It significant in terms both regioselectivity and stereoselectivity, several positional isomers are formed during hydroboration. Given importance this class compounds, an extensive study has been carried out regarding catalytic condition development detailed mechanistic studies selectively obtaining a single isomer. This review comprehensively summarizes regioselective stereoselective hydroboration alkynes. aimed at giving readers accurate knowledge systems available certain We anticipate that inclusive will encourage explore more new types achieve remarkable magnified image
Язык: Английский
Процитировано
94Coordination Chemistry Reviews, Год журнала: 2022, Номер 459, С. 214456 - 214456
Опубликована: Фев. 21, 2022
Язык: Английский
Процитировано
48Chemical Society Reviews, Год журнала: 2022, Номер 51(3), С. 869 - 994
Опубликована: Янв. 1, 2022
This review highlights the hydroelementation reactions of conjugated and separated diynes, which depending on process conditions, catalytic system, as well type reagents, leads to formation various products: enynes, dienes, allenes, polymers, or cyclic compounds. The presence two triple bonds in diyne structure makes these compounds important reagents but selective product is often difficult owing problems associated with maintaining appropriate reaction regio- stereoselectivity. Herein we this topic gain knowledge reactivity diynes systematise range information relating their use reactions. divided according addition E-H (E = Mg, B, Al, Si, Ge, Sn, N, P, O, S, Se, Te) bond bond(s) diyne, reagent used, formed. Not only are comprehensively discussed, synthetic potential obtained products also presented. majority published research included within review, illustrating limitations processes, intent showcase power transformations synthesis materials chemistry.
Язык: Английский
Процитировано
47Dalton Transactions, Год журнала: 2022, Номер 51(8), С. 3027 - 3040
Опубликована: Янв. 1, 2022
Development of efficient Al-complexes and their crucial roles in catalytic selective hydroboration several unsaturated compounds such as carbonyls, alkenes, alkynes, imines, nitriles others were well documented this review.
Язык: Английский
Процитировано
35Chemical Communications, Год журнала: 2021, Номер 57(45), С. 5483 - 5502
Опубликована: Янв. 1, 2021
Recent findings in the chemistry of light actinide metal ions with N-heterocyclic iminato moieties as supporting ligands are described current review article. The emphasis is on catalytic applicability complexes for oxygen containing substrates.
Язык: Английский
Процитировано
37Nature Communications, Год журнала: 2021, Номер 12(1)
Опубликована: Июнь 21, 2021
Abstract Homogeneous earth-abundant metal catalysis based on well-defined molecular complexes has achieved great advance in synthetic methodologies. However, sophisticated ligand, hazardous activator and multistep synthesis starting from base salts are generally required for the generation of active catalysts, which may hinder their broad application large scale organic synthesis. Therefore, development cluster catalysts formed situ simple is importance practical utilization resource, yet it still its infancy. Herein, a mixture catalytic amounts cobalt (II) iodide potassium tert-butoxide discovered to be highly selective hydroboration vinylarenes dihydroboration nitriles, affording good yield diversified products that without isolation can readily undergo further one pot transformations. It should highlighted alkoxide-pinacolborane combination acts as an efficient activation strategy activate metastable heterotopic situ, proposed catalytically species.
Язык: Английский
Процитировано
36Chemistry - A European Journal, Год журнала: 2023, Номер 29(38)
Опубликована: Апрель 20, 2023
A fluorenyl-tethered N-heterocyclic carbene LH (LH=[(Flu)H-(CH2 )2 -NHCDipp ]) and its monoanionic version L- are explored in complexation with zinc towards the hydroboration of N-heteroarenes, carbonyl, ester, amide, nitrile under ambient condition. The N-heteroarenes exhibit high 1,2-regioselectivity which is justified by computational analyses. relative rates differently p-substituted (electron donating vs. withdrawing) pyridines also addressed. monodentate offers a better catalytic activity than chelating for steric reasons despite both giving three-coordinate complexes. mechanism involves Zn-H species at heart these processes trapped Ph2 CO. Computational studies suggest that barrier to form hydride complex comparable required following transfer pyridine.
Язык: Английский
Процитировано
13ChemCatChem, Год журнала: 2022, Номер 15(2)
Опубликована: Ноя. 24, 2022
Abstract This review discusses the immense progress made over recent years in metal‐free catalytic hydroboration. Reactions with several unsaturated functional groups, such as alkynes, alkenes, carbonyl compounds, carbon dioxide, carbodiimides, imines, allenes, pyridines, carboxylic acid derivatives etc., have been explored. Although there are significant developments hydroboration reactions using metal‐based catalysts, strategies more desirable from a sustainability perspective. Considerable effort has by various research groups on catalysts of compounds. Lewis acid, Brønsted acid‐base pairs, and frustrated pairs were involved sources to catalyze sustainable manner. Detailed mechanisms pathways also discussed this review. discussion will provide an overview extent work carried out well indicate scope for future research.
Язык: Английский
Процитировано
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