412300-36-8

Upstream product

• 83816-59-5 3-tert-butyl-2-hydroxy-5-iodobenzaldehyde 
• 170159-24-7 acetylsulfanyl-4-(ethynyl)benzene 
• 69746-43-6 1-iodo-4-thioacetylbenzene 
• 881538-09-6 3-tert-butyl-5-ethynyl-2-hydroxybenzaldehyde 
• 24623-65-2 3-tert-butyl-2-hydroxybenzaldehyde 

Relevant academic research and scientific papers

A practical one-pot synthesis of enantiopure unsymmetrical salen ligands

A practical, one-pot synthesis of enantiopure unsymmetrical salen ligands is described, using a 1:1:1 molar ratio of a chiral diamine and two different salicylaldehydes. The new synthetic protocol can be readily performed in good yields (60-85%) on a mult

POLYMERIC SALEN COMPOUNDS AND METHODS THEREOF

The present disclosure provides a polymerizable compound of the formula (I) where the R1, R2, R’1, R’2, X1 to X8, Y1, Y2, M and L have any of values as defined in the

Synthesis and catalytic properties of p-acylthio(phenylacetylene)n substituted chiral manganese salen complexes

The syntheses of three new salen ligands that are tethered to a p-acylthio(phenylacetylene)n linker are described. The two key steps in the syntheses are coupling of the p-acylthio(phenylacetylene)n linker (n = 0-2) with a 5-iodosali