34125-71-8

Upstream product

• 33143-89-4 1-(1,1-dimethyl-2-propynyloxy)-4-methoxy benzene 
• 115-18-4 2-methyl-3-buten-2-ol 
• 150-76-5 4-methoxy-phenol 
• 164513-96-6 1,1-dimethyl-2-propenyl isobutyl carbonate 

Downstream Products

• 25974-58-7 4-methoxy-2-(3-methylbut-2-enyl)phenol 
• 22927-97-5 6-methoxy-2,2-dimethyl-2H-chromene 

Relevant academic research and scientific papers

Redox-active triazolium-derived ligands in nucleophilic fe-catalysis - Reactivity profile and development of a regioselective o-allylation

Triazolium-derived N-heterocyclic carbene (aNHC) ligands, which are readily accessible by deprotonation of the corresponding triazolium salts, proved to be versatile ligands in diverse allylic substitution reactions. The corresponding triazolium salts are formed from azides and alkynes through the application of 1,3-dipolar cycloaddition and N-alkylation reactions. The unique property of these ligands is to be zwitterionic in their liberated form and to act as strong redox-active σ-donor ligands. By virtue of these qualities, these ligands enable the development of an unprecedented Fe-catalyzed regioselective aryloxylation of allylic carbonates. Copyright

BENZOPYRAN COMPOUND

This invention relates to benzopyran compounds of formula (I) wherein X is NR6, Y is a bond, SO or SO2, Z is C1-4alkyl group or phenyl group, W is hydrogen atom, hydroxy group, C1-6 alkoxy group, a halogen atom,

TRICYCLIC BENZOPYRAN COMPOUND AS ANTI-ARRHYTHMIC AGENTS

This invention relates to benzopyran derivatives of formula (I) or (II), or pharmaceutically acceptable salts thereof wherein R1 and R2 are independently of each other hydrogen atom, C1-6alkyl group or C6-14aryl