96014-51-6

Upstream product

• 88-14-2 2-furanoic acid 
• 74-88-4 methyl iodide 
• 22694-55-9 2,5-dihydrofuran-2-carboxylic acid 

Downstream Products

• 134936-60-0 2-Benzyl-2,5-dihydro-furan-2-carboxylic acid methyl ester 
• 80714-79-0 (α,R,2S)-N-tert-butyl-2,5-dihydro-α-benzamido>-2-furanacetamide 
• 80714-77-8 N-((S)-tert-Butylcarbamoyl-(S)-2,5-dihydro-furan-2-yl-methyl)-N-((R)-1-phenyl-ethyl)-benzamide 
• 80714-76-7 N-((R)-tert-Butylcarbamoyl-(R)-2,5-dihydro-furan-2-yl-methyl)-N-((R)-1-phenyl-ethyl)-benzamide 
• 80714-78-9 N-((R)-tert-Butylcarbamoyl-(S)-2,5-dihydro-furan-2-yl-methyl)-N-((R)-1-phenyl-ethyl)-benzamide 
• 96014-52-7 3-Iodo-4-(4-methoxy-benzyloxycarbonylamino)-tetrahydro-furan-2-carboxylic acid methyl ester 
• 96014-53-8 4-Iodo-3-(4-methoxy-benzyloxycarbonylamino)-tetrahydro-furan-2-carboxylic acid methyl ester 
• 134936-55-3 2-Methyl-2,5-dihydro-furan-2-carboxylic acid methyl ester 
• 96014-54-9 4-(4-Methoxy-benzyloxycarbonylamino)-4,5-dihydro-furan-2-carboxylic acid methyl ester 
• 96093-49-1 4-Amino-4,5-dihydro-furan-2-carboxylic acid 

Relevant academic research and scientific papers

Diastereoselective Diboration of Cyclic Alkenes: Application to the Synthesis of Aristeromycin

The Pt-catalyzed diboration of cyclic alkenes is extended to unsaturated heterocycles and bicyclic compounds and can be accomplished in a diastereoselective fashion. The optimal procedures, substrate scope, and diastereoselectivity were investigated, and examples employing both homogeneous and heterogeneous catalysis were examined. Lastly, application to the construction of the nucleoside analog (±)-aristeromycin was conducted.