55181-35-6

Upstream product

• 495-41-0 1-phenylbut-2-en-1-one 
• 108-98-5 thiophenol 
• 35660-91-4 (E)-1-phenyl-2-buten-1-one 
• 1443045-55-3 4,4,5,5-tetramethyl-2-(phenylthio)-1,3,2-dioxaborolane 
• 882-33-7 diphenyldisulfane 
• 74896-57-4 ethyl 1-methyl-3-oxo-3-phenylpropyl sulphide 
• 77924-06-2 3-[hydroxy(diphenyl)methyl]-N,N-bis(1-methylethyl)pyridine-4-carboxamide 
• 6249-80-5 1-phenylbut-3-en-1-one 

Downstream Products

• 495-41-0 1-phenylbut-2-en-1-one 
• 22956-26-9 4-Methyl-2-phenylbenzo-1-thiopyrylium perchlorate 
• 55181-01-6 2-Methyl-4-phenyl-1-benzo-1-thiopyrylium perchlorate 
• 77988-95-5 trans-3,4-Dihydro-2-methyl-4-phenylbenzo-2H-1-thiopyran 
• 91759-86-3 cis-3,4-Dihydro-2-methyl-4-phenylbenzo-2H-1-thiopyran 
• 77988-92-2 trans-3,4-Dihydro-4-methyl-2-phenyl-2H-1-benzothiopyran 
• 77988-91-1 cis-3,4-Dihydro-4-methyl-2-phenyl-2H-1-benzothiopyran 

Relevant academic research and scientific papers

Catalyst-free chemoselective α-sulfenylation/β-thiolation for α,β-unsaturated carbonyl compounds

A novel, efficient, catalyst-free and product-controllable strategy has been developed for the chemoselective α-sulfenylation/β-thiolation of α,β-unsaturated carbonyl compounds. An aromatic sulfur group could be chemoselectively introduced at α-or β-posit

Thioboration of α,β-unsaturated ketones and aldehydes toward the synthesis of β-sulfido carbonyl compounds

Herein a direct β-sulfido carbonyl compound synthesis by the easy activation of RS-Bpin reagents with α,β-unsaturated ketones and aldehydes is reported. This convenient methodology can be performed at room temperature with no other additives. The key poin

Catalysis by ionic liquid: A simple, green and efficient procedure for the Michael addition of thiols and thiophosphate to conjugated alkenes in ionic liquid, [pmIm]Br

A room temperature ionic liquid, 1-pentyl-3-methylimidazolium bromide, [pmIm]Br efficiently catalyzes Michael addition of thiols and diethyl dithiophosphate to a variety of conjugated alkenes such as α,β- unsaturated carbonyl compounds, carboxylic esters,

OPTICAL INDUCTION - IV Optical Induction by Using Homogeneous Catalyst

Better optical induction during Michael addition has been achieved by using new homogeneous catalysts based on quinine and quinidine.

Synthesis of Heterocyclic Compounds : Part XXIV - Synthesis of 2,4-Disubstituted Thianaphthalenium Perchlorates and Thiachromans

Cyclodehydration of β-phenylmercaptopropyl phenyl ketone (V) and β-phenyl-β-phenylmercaptoethyl methyl ketone (VI) with 70percent perchloric acid gives a mixture of 2-methyl-4-phenylthianaphthalenium perchlorate (X), 4-methyl-2-phenylthianaphthalenium per