607708-29-2

Upstream product

• 607708-11-2 2,6-dihydroxy-4-[(phenylthio)methyl]nicotinonitrile 
• 441052-94-4 {2,6-dichloro-4-[(phenylsulfinyl)methyl]pyridin-3-yl}(4-methylphenyl)methanone 
• 607708-13-4 {2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanol 
• 607708-16-7 {2,6-dichloro-4-[(phenylthio)methyl]pyridin-3-yl}(4-methylphenyl)methanone 
• 441052-90-0 2,6-dichloro-4-[(phenylthio)methyl]nicotinonitrile 
• 441052-91-1 2,6-dichloro-4-[(phenylthio)methyl]nicotinaldehyde 
• 624-48-6 dimethyl cis-but-2-ene-1,4-dioate 

Downstream Products

• 607708-30-5 dimethyl 1,3-dichloro-5-methoxy-8-(4-methylphenyl)isoquinoline-6,7-dicarboxylate 

Relevant academic research and scientific papers

A sequential Pummerer-Diels-Alder route for the generation and trapping of furo[3,4-c]pyridines: Synthesis of heterocyclic analogues of 1-arylnaphthalene lignans

The Pummerer reaction of an o-benzoyl-substituted pyridylmethyl sulfoxide generates an α-thio-carbocation, the interception of which by a neighboring keto functionality produces an α-thio-substituted furo[3,4-c]pyridine as transient intermediate; the latt