45941-97-7

Upstream product

• 288-88-0 1,2,4-Triazole 
• 149509-26-2 1-chloro-2-(4-fluorophenyl)-3-trimethylsilyl-2-propanol 
• 107-18-6 allyl alcohol 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 107-19-7 propargyl alcohol 
• 352-13-6 4-flourophenylmagnesium bromide 
• 350-40-3 2-(4-fluorophenyl)-1-propene 
• 2967-83-1 p-fluoro-α-methylstyrene oxide 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 132993-23-8 4-fluorophenyl trifluoromethanesulfonate 
• 18511-62-1 4-fluorostyrene oxide 
• 2181-42-2 trimethylsulphonium iodide 
• 403-33-8 methyl 4-flurobenzoate 
• 456-04-2 2-Chloro-4'-fluoroacetophenone 

Downstream Products

• 132927-05-0 1-(3-bromoprop-1-en-2-yl)-4-fluorobenzene 
• 1258011-48-1 (2-(4-fluorophenyl)allyloxy)trimethylsilane 
• 1325729-49-4 2-(2-(4-fluorophenyl)allyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1453102-73-2 3-bromo-2-(4-fluorophenyl)propane-1,2-diol 
• 1453102-55-0 (S)-3-bromo-2-(4-fluorophenyl)propane-1,2-diol 
• 106191-62-2 β-(4-fluorophenyl)-β-methyleneethanamine 
• 1447974-61-9 5-(chloromethyl)-5-(4-fluorophenyl)oxazolidin-2-one 
• 1447974-70-0 5-(chloromethyl)-5-(4-fluorophenyl)oxazolidin-2-one 
• 1447974-52-8 tert-butyl (2-(4-fluorophenyl)allyl)carbamate 
• 1596248-12-2 (R)-2-benzyl-2-(2-(4-fluorophenyl)allyl)cyclohexan-1-one 
• 1639790-54-7 3-(1,3-dithiolan-2-ylidene)-5-(4-fluorophenyl)hex-5-en-2-one 
• 1639790-62-7 (E)-4-(1,3-dithiolan-2-ylidene)-6-(4-fluorophenyl)-1-(4-(trifluoromethyl)phenyl)hepta-1,6-dien-3-one 
• 1639790-32-1 ethyl 2-(4-fluorophenyl)allyl carbonate 

Relevant academic research and scientific papers

Synthesis of Six-Membered Spiro Azacyclic Oxindole Derivatives via a One-Pot Process of Umpolung Allylation/Aza-Prins Cyclization

An unprecedented synthetic approach involving umpolung allylation/aza-Prins cyclization of N-2,2,2-trifluoroethylisatin ketimines is described. The reactions proceed smoothly with allyl bromide in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene, H2O, and trimethylsilyl bromide; this one-pot protocol allows access to six-membered spiro azacyclic oxindole derivatives in good to excellent yields. Notably, while the general aza-Prins cyclization involves amines and aldehydes, the present synthetic strategy represents the first aza-Prins cyclization that utilizes the umpolung property of N-2,2,2-trifluoroethylisatin ketimines.

Asymmetric Reductive and Alkynylative Heck Bicyclization of Enynes to Access Conformationally Restricted Aza[3.1.0]bicycles

Conformationally restricted azabicycles are becoming increasingly important in medicinal research. Asymmetric Heck bicyclization of enynes proceeds to give medicinally useful aza[3.1.0] and aza[4.1.0] bicycles with excellent enantioselectivity. The key organopalladium species after bicyclization can be trapped by silanes and terminal alkynes.

Mild Iridium-Catalysed Isomerization of Epoxides. Computational Insights and Application to the Synthesis of β-Alkyl Amines

The isomerization of epoxides to aldehydes using the readily available Crabtree's reagent is described. The aldehydes were transformed into synthetically useful amines by a one-pot reductive amination using pyrrolidine as imine-formation catalyst. The reactions worked with low catalyst loadings in very mild conditions. The procedure is operationally simple and tolerates a wide range of functional groups. A DFT study of its mechanism is presented showing that the isomerization takes place via an iridium hydride mechanism with a low energy barrier, in agreement with the mild reaction conditions. (Figure presented.).

Palladium-catalyzed allylic C-H oxidation under simple operation and mild conditions

We discovered an effective and simple system (Pd/BQ/air/r.t.) for making allylic alcohols through Pd-catalyzed allylic C-H bond functionalization. This approach exhibits advantages due to its simple operation, mild conditions, and environmentally benign features. By modifying reaction conditions, it can be suitable for preparing unsaturated aldehydes, allylic esters, ethers, and amines.

Palladium-Catalyzed Regioselective Aerobic Allylic C?H Oxygenation: Direct Synthesis of α,β-Unsaturated Aldehydes and Allylic Alcohols

A protocol for the synthesis of α,β-unsaturated aldehydes and allylic alcohols from simple allylic hydrocarbons with water via palladium-catalyzed functionalization of allylic C?H bonds was described. Molecular oxygen is utilized as the sole oxidant in this oxygenation of terminal alkenes. This protocol features good functional group compatibility, broad substrate scope, and high atom- and step-economy. Moreover, the synthetic utility of this method can be highlighted by its application to the synthesis of ibuprofen, which is a highly potent analgesic. (Figure presented.).

Traversing Steric Limitations by Cooperative Lewis Base/Palladium Catalysis: An Enantioselective Synthesis of α-Branched Esters Using 2-Substituted Allyl Electrophiles

Cooperative catalysis enables the direct enantioselective α-allylation of linear prochiral esters with 2-substituted allyl electrophiles. Critical to the successful development of the method was the recognition that metal-centered reactivity and the sourc

An enyne cycloisomerization/[5+1] reaction sequence to synthesize tetrahydroisoquinolinones from enyne-enes and CO

An enyne cycloisomerization/[5+1] reaction sequence was developed to synthesize tetrahydroisoquinolinones from linear enyne-enes and CO. The first step is a gold(i)-catalyzed enyne cycloisomerization, generating six-membered-ring-fused vinylcyclopropanes. The second step is a rhodium(i)-catalyzed [5+1] reaction of vinylcyclopropanes with CO. This two-step reaction could also be carried out in one-pot without isolating the cycloisomerization product generated from the first step of this sequence.

Enantioselective bromocyclization of allylic amides catalyzed by BINAP derivatives

A highly enantioselective bromocyclization of allylic amides with N-bromosuccinimide (NBS) was developed with DTBM-BINAP as a catalyst, affording chiral oxazolines with a tetrasubstituted carbon center in high yield with up to 99% ee. By utilizing the bro

Regioselective ring-opening α-methylenation of aryl epoxides to conjugated allyl alcohols utilizing n-BuLi and Me2S=CH2 reagents

In the presence of a mixture of n-BuLi and Me2SCH2 reagents, aryl epoxides underwent a novel ring-opening α-methylenation providing conjugated allyl alcohols with an unusual regioselective pattern.

Palladium-catalyzed oxidative heck-type allylation of β,β- disubstituted enones with allyl carbonates

The palladium-catalyzed oxidative Heck-type allylation of β,β-disubstituted enones, i.e., α-oxoketene dithioacetals, was efficiently realized with allyl carbonates, providing a concise route to highly functionalized dienes. The present synthetic methodology utilizes the substrate activation strategy to activate the C-H bond of β,β-disubstituted enones by introduction of a 1,2-dithiolane functionality to make the enone substrate highly polarized and thus increase its reactivity, demonstrating rare examples for transition metal-catalyzed allylic substitution of ss,ss-disubstituted enones through a Heck-type allylation process.