880644-70-2

Upstream product

• 608515-48-6 N-(2-bromobenzyl)-2,2-diethoxyacetamide 
• 608515-49-7 8-bromoisoquinolin-3-ol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 880644-73-5 8-(p-anisyl-p-phenyl)isoquinolin-3-ol 
• 880644-74-6 8-(p-anisyl-p-phenyl)isoquinolin-3-yl trifluoromethanesulfonate 
• 880644-75-7 8,8'-bis(p-anisyl-p-phenyl)-3,3'-biisoquinoline 
• 880644-72-4 8-(p-anisyl-p-phenyl)isoquinolin-3-yl benzoate 

Relevant academic research and scientific papers

A new family of biisoquinoline chelates

Four 8,8′-diaryl-substituted 3,3′-biisoquinoline ligands have been synthesized and characterized. The key feature of this new family of chelates is their endotopic but sterically non-hindering nature. All four ligands were made from a common 8-bromoisoquinolin-3-ol precursor; between three and twelve synthetic steps were necessary to obtain the products. The reported synthetic procedures allow for gram-scale production of these biisoquinolines. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

Sterically non-hindering endocyclic ligands of the bi-isoquinoline family

Bi-isoquinoline can be used as a building block to prepare a new family of non-sterically hindering chelates, including a macrocyclic system; the endocyclic nature of the ligands has been confirmed by the X-ray structure of an octahedral tris-chelate iron