332940-30-4

Upstream product

• 497-23-4 2-buten-4-olide 

Downstream Products

• 332940-52-0 [3-(4-allyl-5-oxo-tetrahydro-furan-3-yl)-3-phenyl-propenyl]-(4-methoxy-phenyl)carbamic acid tert-butyl ester 
• 332940-45-1 (4-Methoxy-phenyl)-[(Z)-(S)-3-((3S,4S)-4-methyl-5-oxo-tetrahydro-furan-3-yl)-3-phenyl-propenyl]-carbamic acid tert-butyl ester 
• 332940-56-4 3-allyl-4-(1-phenyl-but-3-enyl)-dihydro-furan-2-one 
• 332940-54-2 3-(4-allyl-5-oxo-tetrahydro-furan-3-yl)-3-phenyl-propionaldehyde 
• 332940-48-4 3-allyl-4-(1-phenyl-allyl)-dihydro-furan-2-one 
• 332940-35-9 4-(3-bromo-1-phenyl-propyl)-dihydro-furan-2-one 
• 332940-34-8 4-(3-hydroxy-1-phenyl-propyl)-dihydro-furan-2-one 
• 332940-46-2 4-(1-phenyl-allyl)-dihydro-furan-2-one 
• 332940-50-8 4-phenyl-3',4,7,7'-tetrahydro-3H-isobenzofuran-1-one 
• 332940-33-7 3-(4'-furanone)benzenepropanal 

Relevant academic research and scientific papers

Kinetic resolution of racemic lactones by conjugate additions of allylic organolithium species: Direct formation of three contiguous centers with high diastereo- and enantioselectivities

(Matrix presented) Kinetic resolution of racemic α,β-unsaturated lactones by the organolithium species produced from asymmetric lithiation of N-Boc-N-(p-methoxyphenyl)cinnamylamine provides conjugate addition products with three contiguous stereogenic centers in yields of 62-77% with diastereomeric ratios from 75:25 to >99:1 and enantiomeric ratios for the major diastereomers from 94:6 to 98:2.