862170-87-4

Upstream product

• 862170-68-1 3-benzyl-4-methylene-tetrahydro-furan-3-carboxylic acid 
• 786682-63-1 methyl 3-benzyl-4-methylenetetrahydrofuran-3-carboxylate 
• 508181-17-7 methyl (2E)-3-phenyl-2-(prop-2-yn-1-yloxymethyl)prop-2-enoate 

Relevant academic research and scientific papers

Synthesis of 3,4-disubstituted 2,5-dihydrofurans starting from the Baylis-Hillman adducts via consecutive radical cyclization, halolactonization, and decarboxylation strategy

A facile synthetic method of 3,4-disubstituted 2,5-dihydrofurans and 2,5-dihydropyrroles starting from the Baylis-Hillman adducts was developed. The 2,5-dihydrofuran skeleton was constructed via the consecutive radical cyclization, hydrolysis, halolactonization, and spontaneous decarboxylation strategy starting from the modified Baylis-Hillman adducts.