171626-75-8

Upstream product

• 56164-42-2 3-chloro-1H-pyrrole-2-carbaldehyde 
• 171626-92-9 1-[3-Chloro-1-(toluene-4-sulfonyl)-1H-pyrrol-2-yl]-ethanol 
• 171626-91-8 2-acetyl-3-chloro-1-tosylpyrrole 
• 171626-90-7 3-chloro-2-formyl-1-(p-toluenesulfonyl)pyrrole 
• 98-59-9 p-toluenesulfonyl chloride 
• 699-13-8 (tetrahydropyranyloxy)acetaldehyde 
• 171626-93-0 1-[3-Chloro-1-(toluene-4-sulfonyl)-1H-pyrrol-2-yl]-3-hydroxy-4-(tetrahydro-pyran-2-yloxy)-butan-1-one 

Downstream Products

• 171626-83-8 7-{5-[3-Chloro-1-(toluene-4-sulfonyl)-1H-pyrrol-2-yl]-3-methoxy-furan-2-yl}-4,5-dihydro-indole-1-carboxylic acid tert-butyl ester 
• 171626-79-2 2-(1-{5-[3-Chloro-1-(toluene-4-sulfonyl)-1H-pyrrol-2-yl]-3-methoxy-furan-2-yl}-vinyl)-pyrrole-1-carboxylic acid tert-butyl ester 
• 188491-48-7 3-Chloro-2-(5-cyclohexylidenemethyl-4-methoxy-furan-2-yl)-pyrrole-1-carboxylic acid tert-butyl ester 
• 171626-78-1 3-Chloro-2-[5-(cyclohexyl-hydroxy-methyl)-4-methoxy-furan-2-yl]-pyrrole-1-carboxylic acid tert-butyl ester 
• 171626-77-0 [5-(3-Chloro-1H-pyrrol-2-yl)-3-methoxy-furan-2-yl]-cyclohexyl-methanol 
• 171626-76-9 3-Chloro-2-(4-methoxy-furan-2-yl)-1-(toluene-4-sulfonyl)-1H-pyrrole 

Relevant academic research and scientific papers

Synthesis of various model compounds for the conjugated heterocyclic ring system of antibiotic roseophilin

The title synthesis was accomplished starting with 3-chloro-2-formylpyrrole. The synthetic scheme featured one-pot preparation of the 4-methoxy-2-(pyrrol-2-yl)furan from the 2-acetoacetylpyrrole and coupling reactions of the C5-position of the