244608-10-4

Upstream product

• 64957-80-8 3-methoxy-2-vinylbenzoic acid 
• 244608-08-0 3-benzyloxy-5-hydroxy-4-iodobenzoic acid benzyl ester 
• 143123-58-4 2-(3-Methoxy-2-vinylphenyl)-4,4-dimethyl-2-oxazoline 
• 1521-38-6 2,3-dimethoxybenzoic acid 
• 144034-41-3 N-(1-hydroxy-2-methylpropan-2-yl)-2,3-dimethoxybenzamide 
• 7169-06-4 2,3-dimethoxybenzoyl chloride 
• 57598-32-0 4,5-dihydro-2-(2',3'-dimethoxyphenyl)-4,4-dimethyloxazole 

Downstream Products

• 244608-12-6 1-benzyloxy-10-methoxy-11-methylene-6-oxo-6,11-dihydro-dibenzo[b,e]oxepine-3-carboxylic acid benzyl ester 
• 244608-08-0 3-benzyloxy-5-hydroxy-4-iodobenzoic acid benzyl ester 
• 18713-43-4 3-hydroxy-4-methoxy-1(3H)-isobenzofuranone 
• 244608-07-9 3,5-Bis-benzyloxy-4-[1-(2-benzyloxycarbonyl-6-methoxy-phenyl)-vinyl]-benzoic acid benzyl ester 
• 437614-02-3 3-Benzyloxy-5-(3-benzyloxy-2-vinyl-benzoyloxy)-4-iodo-benzoic acid benzyl ester 

Relevant academic research and scientific papers

Application of an intramolecular heck reaction for the construction of the balanol aryl core structure

The highly functionalized aryl core structure of balanol has been synthesized employing a regioselective intramolecular Heck reaction as the key step. This approach can potentially lead to new types of analogues of the potent PKC inhibitor.