17275-85-3

Upstream product

• 85565-93-1 2-bromo-3,5-dimethoxy-benzaldehyde 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 64-17-5 ethanol 
• 17275-86-4 2-bromo-3,5-dimethoxybenzoic acid 
• 17275-82-0 ethyl 3,5-dimethoxybenzoate 
• 17275-84-2 2-amino-3,5-dimethoxy-benzoic acid ethyl ester 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 17275-83-1 3,5-dimethoxy-2-nitro-benzoic acid ethyl ester 

Downstream Products

• 17275-86-4 2-bromo-3,5-dimethoxybenzoic acid 
• 17276-03-8 1,3,6,8-tetramethoxynaphthalene 
• 17275-87-5 2-Brom-3.5-dimethoxy-benzoylchlorid 
• 17276-06-1 2-Brom-3.5-dimethoxy-benzamid 
• 17275-96-6 2-Brom-3,5-dimethoxy-phenylacetylchlorid 
• 17275-88-6 2-Brom-3.5-dimethoxy-benzoyl-diazomethan 
• 17275-78-4 2-Brom-3,5-dimethoxy-phenylessigsaeure-methylester 
• 17275-79-5 2-bromo-3,5-dimethoxyphenylacetic acid 
• 17275-89-7 2-Acetyl-6-brom-3,5-dimethoxy-phenylessigsaeure-methylester 
• 17275-97-7 2-<2-Brom-3,5-dimethoxy-phenylacetyl>-acetessigsaeure-aethylester 

Relevant academic research and scientific papers

Synthesis of Axially Chiral 2,2′-Bisphosphobiarenes via a Nickel-Catalyzed Asymmetric Ullmann Coupling: General Access to Privileged Chiral Ligands without Optical Resolution

We report an asymmetric homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates resulting in highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates. These products are readily converted to enantioenriched b