scholarly journals Metal‐Free Deoxygenation of Amine N–Oxides: Synthetic and Mechanistic Studies

ChemPhysChem ◽  
2021 ◽  
Author(s):  
Sami Lakhdar ◽  
William Lecroq ◽  
Jules Schleinitz ◽  
Mallaury Billoue ◽  
Anna Perfetto ◽  
...  
2021 ◽  
Author(s):  
Shi-Chao Lu ◽  
Fuqiang Wen ◽  
Xidong Guan

A metal-free redox arylation of alkynes with sulfoxides has been developed to provide an unconventional access to diverse γ-arylated 1,3-dicarbonyl compounds in an atom-economical manner. Mechanistic studies suggest that a...


Synlett ◽  
2017 ◽  
Vol 28 (15) ◽  
pp. 2018-2023 ◽  
Author(s):  
Xiang Fang ◽  
Xueyan Yang ◽  
Tongle Shao ◽  
Jun Zhou ◽  
Chen Jin ◽  
...  

A metal-free oxidative coupling reaction of trifluoromethyl β-diketones with alcohols for the synthesis of α-keto esters in good to excellent yields has been developed. Preliminary mechanistic studies suggest that an I2/TBHP promoted sequential iodination, C–C bond cleavage, C–O bond formation and oxidation pathway is involved in this reaction.


Synlett ◽  
2017 ◽  
Vol 28 (13) ◽  
pp. 1558-1563 ◽  
Author(s):  
Aiwen Lei ◽  
Atul Singh ◽  
Hong Yi ◽  
Guoting Zhang ◽  
Changliang Bian ◽  
...  

We have developed a photoinduced oxidative cross-coupling of thiophenols with alcohols for O–S bond formation. The protocol uses visible light, a metal-free photocatalyst, and oxygen as the oxidant for the selective synthesis of alkyl benzenesulfonates; no ligand co-additive is necessary. Mechanistic studies suggested that the disulfide and alkyl benzenesulfinate are involved as intermediates and that the transformation proceeds by a radical pathway.


2015 ◽  
Vol 6 (5) ◽  
pp. 2943-2951 ◽  
Author(s):  
Eiji Yamamoto ◽  
Satoshi Ukigai ◽  
Hajime Ito

A transition-metal-free method has been developed for the boryl substitution of functionalized aryl-, heteroaryl- and alkenyl halides using a silylborane/alkoxy-base reagent. Borylation of (Z)-alkenyl halides proceeded in a stereoretentive manner.


Synlett ◽  
2019 ◽  
Vol 30 (15) ◽  
pp. 1805-1809
Author(s):  
Shuai Li ◽  
Xia Wang ◽  
Xin-Ge Yang ◽  
Gui-Quan Yu ◽  
Xue-Qiang Wang

A transition-metal-free etherification protocol that is capable of synthesizing deuterated ethers is described. A wide range of aryl alkyl ethers and thioethers were suitable for this transformation owing to the mild reaction conditions. Besides, a series of sterically bulky deuterated alcohols were successfully incorporated into cyano-substituted arenes. The results of mechanistic studies suggested this reaction might take place via nucleophilic aromatic substitution pathway.


Synlett ◽  
2020 ◽  
Vol 31 (19) ◽  
pp. 1857-1861
Author(s):  
Hua Zhang ◽  
Li Wang

In recent decades, C–H borylation has undergone rapid development and has become one of the most important and efficient methods for the synthesis of organoboron compounds. Although transition-metal catalysis dominates C–H borylation, the metal-free approach has emerged as a promising alternative strategy. This article briefly summarizes the history of metal-free aromatic C–H borylation, including early reports on electrophilic C–H borylation and recent progress in metal-free catalytic intermolecular C–H borylation; it also highlights our recent work on BF3·Et2O-catalyzed C2–H borylation of hetarenes. Despite these recent advances, comprehensive mechanistic studies on various metal-free catalytic aromatic C–H borylations and novel processes with a wider substrate scope are eagerly expected in the near future.


2013 ◽  
Vol 135 (2) ◽  
pp. 941-947 ◽  
Author(s):  
Adrian Y. Houghton ◽  
Virve A. Karttunen ◽  
Cheng Fan ◽  
Warren E. Piers ◽  
Heikki M. Tuononen

2017 ◽  
Vol 53 (94) ◽  
pp. 12708-12711 ◽  
Author(s):  
Redouane Beniazza ◽  
Baptiste Abadie ◽  
Lionel Remisse ◽  
Damien Jardel ◽  
Dominique Lastécouères ◽  
...  

Cross dehydrogenative couplings on ethers are performed very effectively in a one-pot process using NFSI as oxidizing agent under low-intensity UVA irradiation in the presence of 2 mol% benzophenone.


2016 ◽  
Vol 7 (9) ◽  
pp. 5680-5685 ◽  
Author(s):  
Clément Chauvier ◽  
Pierre Thuéry ◽  
Thibault Cantat

In the presence of dialkylboranes, formic acid is converted to formaldehyde and methanol derivatives. This is the first example of formate disproportionation under metal-free conditions. Mechanistic studies highlight the role of transient borohydrides in the reduction of formates and this is further shown in transfer hydroboration for aldehyde reduction.


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