20365-71-3

Upstream product

• 2314-48-9 (S,S)-dimethyl trithiocarbonate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 75-15-0 carbon disulfide 
• 74-88-4 methyl iodide 

Downstream Products

• 1142124-83-1 3-(4-methoxybenzoyl)-2H-chromene-2-thione 
• 40888-66-2 3-(4-methoxybenzoyl)-2H-1-benzopyran-2-one 
• 1228956-76-0 3-(4-methoxybenzoyl)-8-methoxy-2H-chromene-2-thione 
• 101737-12-6 8-methoxy-3-(4-methoxy-benzoyl)-coumarin 
• 1255769-91-5 3-(4-methoxybenzoyl)-6-nitro-2H-chromene-2-thione 
• 1263317-23-2 (4-methoxyphenyl)(3-thioxo-3H-benzo[f]chromen-2-yl)methanone 
• 1228956-82-8 3-(4-methoxybenzoyl)-6-bromo-2H-chromene-2-thione 
• 1245726-72-0 6-bromo-3-(4-methoxybenzoyl)-2H-chromen-2-one 
• 532-11-6 anethole trithione 

Relevant academic research and scientific papers

Et3N mediated synthesis of polysubstituted thiophenes from α-oxo ketene dithioacetals

In this Letter, an efficient synthetic route to prepare polysubstituted thiophene derivatives was achieved via the Et3N-mediated (Claisen) rearrangement reaction from α-oxo S-methyl-S-propargyl ketenes, which were obtained through alkylation of

Influence of the ligand frameworks on the coordination environment and properties of new phenylmercury(II) β-oxodithioester complexes

New phenylmercury(ii) complexes of the form [PhHg(L1), PhHg(L2) and PhHg(L3)] (L1 = methyl-3-hydroxy-3-(p-methoxyphenyl)-2-propenedithioate (1), L2 = methyl-3-hydroxy-3-(p-bromophenyl)-2-propenedithioate (2) and L3 = methyl-3-hydroxy-(3-pyridyl)-2-propene

New planar trans-copper(II) β-dithioester chelate complexes: synthesis, characterization, anticancer activity and DNA-binding/cleavage studies

New planar trans-copper(II) β-dithioester complexes, [Cu(L)2] (L?=?methyl-3-hydroxy-(3-pyridyl)-2-propenedithioate (L1 in 1), methyl-3-hydroxy-(2-naphthyl)-2-propenedithioate (L2 in 2), methyl-3-hydroxy-3-(p-methoxyphenyl)-2-propenedithioate (L

Synthesis and characterization of new square planar heteroleptic cationic complexes [Ni(ii) β-oxodithioester-dppe]+; Their use as a catalyst for Chan-Lam coupling

Novel heteroleptic [Ni(ii) β-oxodithioester-dppe]+PF6- complexes (β-oxodithioester = methyl-3-hydroxy-3-benzyl-2-propenedithioate L1 1, methyl-3-hydroxy-3-(p-methoxyphenyl)-2-propenedithioate L2 2, methyl-3-hydroxy-3-(naphthyl)-2-propenedithioate L3 3, methyl-3-hydroxy-3-(p-chlorophenyl)-2-propenedithioate L4 4, methyl-3-hydroxy-3-(p-bromophenyl)-2-propenedithioate L5 5 and methyl-3-hydroxy-3-(p-cyanophenyl)-2-propenedithioate L6 6) have been synthesized and characterized by elemental (C, H, N) analysis, ESI-MS, IR, UV-visible, 1H, 13C{1H}, 31P{1H} and 19F{1H} NMR spectroscopy. The distorted square planar structures of the isomorphous cationic complexes 2, 3, 4 and 5 have been determined by X-ray crystallography. The catalytic activities of 1-6 were investigated for the Chan-Lam coupling reaction involving arylboronic acids and amines to afford N-arylated products in good to excellent yields under mild conditions with 1 mol% catalyst loading. This catalytic protocol offers significant functional group tolerance, and is endowed with a broad substrate scope. This journal is

Catalytic activity of new heteroleptic [Cu(PPh3)2(β-oxodithioester)] complexes: Click derived triazolyl glycoconjugates

A series of four new and two known luminescent heteroleptic Cu(i) complexes of the form [Cu(PPh3)2(β-oxodithioester)] (β-oxodithioester = methyl-3-hydroxy-3-(2-furyl)-2-propenedithioate L1 1, methyl-3-hydroxy-3-(2-thienyl)-2-propened

Half-sandwich titanium complexes with β-oxodithioester ligands

The reaction of CpTiCl3with HLx[HLx= methyl 3-(4′-X-phenyl)-3-hydroxy-2-propenedithioate ligands; X = H(1), Me(2), OMe(3), Cl(4), Br(5)] in the presence of NEt3yielded the corresponding half-sandwich complexes T

An expedient route to highly functionalized 2H-chromene-2-thiones via ring annulation of β-oxodithioesters catalyzed by InCl3 under solvent-free conditions

A convenient and one-pot synthesis of 3-aroyl/heteroaroyl-2H-chromene-2- thiones and benzo[f]2H-chromene-2-thiones has been developed by the condensation of β-oxodithioesters and salicylaldehydes/α-hydroxynaphthaldehydes in the presence of indium trichlor