68090-03-9

Upstream product

• 874-90-8 4-methoxybenzonitrile 

Downstream Products

• 838-34-6 2-(p-methoxyphenyl)benzoxazole 
• 68723-61-5 3,5-di((p-methoxy)phenyl)-1,2,4-selenadiazole 
• 70250-32-7 2,5-bis-(4-methoxy-phenyl)-[1,3,4]selenadiazole 
• 69625-91-8 2-(4-methoxyphenyl)-4-phenyl-1,3-selenazole 
• 2393-23-9 4-methoxy-benzylamine 
• 69625-90-7 2-(4-methoxy-phenyl)-4-methyl-selenazole 
• 75103-38-7 2-(4-methoxy-phenyl)-4H-pyrrolo[3,2-d]selenazole-5-carboxylic acid ethyl ester 
• 75103-20-7 [2-(4-methoxy-phenyl)-selenazol-4-yl]-methanol 
• 75103-32-1 2-azido-3-[2-(4-methoxy-phenyl)-selenazol-4-yl]-acrylic acid ethyl ester 
• 75103-26-3 2-(4-methoxy-phenyl)-selenazole-4-carbaldehyde 
• 129303-38-4 (2S,6S)-2,6-Dicyclohexyl-4-(4-methoxy-phenyl)-6H-[1,3,5]oxaselenazine 
• 129303-38-4 (2S,6R)-2,6-Dicyclohexyl-4-(4-methoxy-phenyl)-6H-[1,3,5]oxaselenazine 
• 6265-92-5 2-(4-methoxy-phenyl)-benzothiazole 

Relevant academic research and scientific papers

Reduction of selenoamides to amines using SmI2-H2O

Selenoamides are selectively reduced to amines by SmI2 with H2O. The process is general for primary, secondary, and tertiary aryl and alkyl selenoamide substrates and selectively delivers amine products. The reduction proceeds under mild conditions using SmI2 activated by straightforward addition of H2O, and does not require an additional Lewis base additive.

Synthesis, characterization and antibacterial activity of some new ferrocenyl selenazoles and 3,5-diferrocenyl-1,2,4-selenadiazole

New ferrocenyl containing selenazole derivatives were synthesized from reactions of aryl selenocarboxamide (i.e. Ar-CSe(NH2); ArC6H5 (1), 4-Br-C6H4 (2), 4-PhC6H4 (3), 4-CH3

Synthesis of primary arylselenoamides by reaction of aryl nitriles with Woollins' reagent

The reaction of aryl nitriles with Woollins' reagent followed by water affords a variety of primary arylselenoamides In 60-100% yield. The first crystal structures of two primary selenoamides are reported.

Palladium-catalyzed formation of 3,5-diaryl-1,2,4-selenadiazoles from arylselenocarboxamide

A number of new and known arylselenocarboxamides (i.e. Ar-C(=Se)NH2; Ar=C6H5 (1), 4-BrC6H4 (2), 2-MeOC6H4 (3), 4-MeOC6H4 (4), 4-MeSC6H4/sub

A facile preparation of aliphatic and aromatic primary selenoamides using 4-methylselenobenzoate as a new selenating reagent

Aliphatic and aromatic primary selenoamides 2 were isolated by the reaction of the corresponding aliphatic and aromatic nitriles with potassium 4-methylselenobenzoate in the presence of BF3·Et2O in moderate from high yields.

Convenient synthesis of primary selenoamides from aryl nitriles, selenium and sodium borohydride

Aryl nitriles react smoothly with sodium hydrogen selenide, itself prepared in situ from selenium and sodium borohydride, in ethanol to give the corresponding primary selenoamides in moderate to good yield.

Synthesis of primary selenocarboxamides and conversion of alkyl selenocarboxamides into selenazoles

Nitriles react with sodium hydrogen selenide, pyridine and hydrochloric acid in ethanol to give primary aryl and alkyl selenocarboxamides. The alkyl selenocarboxamides are converted into selenazoles by reaction with phenacyl bromide.

A Novel Synthesis of Primary Selenoamides from Nitriles by the Treatment of Bis(trimethylsilyl) Selenide and BF3*OEt2

Reaction of nitriles with (Me3Si)2Se in the presence of BF3*OEt2 afforded the corresponding primary selenoamides in moderate yields.A selenourea and a selenothiocarbamate were also prepared in a similar manner from the corresponding cyanamide and thiocyanate.