53138-48-0

Upstream product

• 1008-76-0 4,5-dihydro-5-phenyl-2(3H)-furanone 
• 882-33-7 diphenyldisulfane 
• 103-04-8 (phenylthio)acetic acid 
• 96-09-3 styrene oxide 

Downstream Products

• 1326304-37-3 3-benzyl-5-phenylfuran-2-yl phenyl carbonate 
• 1326304-38-4 3-benzyl-5-phenylfuran-2-yl 2,2,2-trichloroethyl carbonate 
• 1326304-42-0 3-ethyl-5-phenylfuran-2-yl phenyl carbonate 
• 1326304-44-2 3-(4-bromobenzyl)-5-phenylfuran-2-yl phenyl carbonate 
• 1326304-46-4 3-allyl-5-phenylfuran-2-yl phenyl carbonate 
• 1326304-49-7 2,2,2-trichloroethyl (R)-3-benzyl-2-oxo-5-phenyl-2,3-dihydrofuran-3-carboxylate 
• 1326304-50-0 2,2,2-trichloroethyl 4-benzyl-5-oxo-2-phenyl-2,5-dihydrofuran-2-carboxylate 
• 1326304-59-9 phenyl (R)-3-allyl-2-oxo-5-phenyl-2,3-dihydrofuran-3-carboxylate 
• 15121-75-2 3-methyl-5-phenylfuran-2-(5H)-one 
• 15121-74-1 3-methyl-5-phenylfuran-2(3H)-one 
• 60492-51-5 3-ethyl-5-phenylfuran-2(5H)-one 
• 336800-61-4 3-benzyl-5-phenylfuran-2(5H)-one 
• 7505-06-8 3-benzyl-5-phenylfuran-2(3H)-one 

Relevant academic research and scientific papers

Isothiourea-catalyzed asymmetric O- to C-carboxyl transfer of furanyl carbonates

The ability of a chiral isothiourea to promote the regio- and enantioselective O- to C-carboxyl transfer of a series of 3-alkyl-5-aryl- and 5-methyl-3-phenylfuranyl carbonates is examined, generating preferentially the -regioisomers (α/γ up to 83:17) with high asymmetric induction (up to 83% ee). Georg Thieme Verlag Stuttgart - New York.