914366-90-8

Upstream product

• 76638-09-0 (2R,3S)-2-methyl-3-phenyloxirane-2-carbaldehyde 
• 15174-47-7 α-methyl-trans-cinnamaldehyde 
• 58550-28-0 (2E,4E)-ethyl 4-methyl-5-phenylpenta-2,4-dienoate 
• 914366-74-8 (S,E)-ethyl 4-hydroxy-4-((S)-hydroxy(phenyl)methyl)pent-2-enoate 
• 914366-82-8 (E)-ethyl 3-((4S,5S)-4-methyl-2-oxo-5-phenyl-1,3-dioxolan-4-yl)acrylate 
• 111120-83-3 Ethyl (4S,5S)-4,5-epoxy-2-methyl-3-phenylpropanal 

Relevant academic research and scientific papers

De novo synthesis of 2-substituted syn-1,3-diols via an iterative asymmetric hydration strategy

(Chemical Equation Presented) The enantioselective syntheses of several protected 4-substituted syn-3,5-dihydroxy carboxylic esters have been achieved from the corresponding achiral (E,E)- or (E,Z)-1,3-dienoates. The route relies upon an enantio- and regi

Palladium-Catalyzed Selective Hydrogenolysis of Alkenyloxiranes with Formic Acid. Stereoselectivity and Synthetic Utility

Selective hydrogenolysis of alkenyloxiranes to give homoallylic alcohols was carried out using formic acid in the presence of palladium-phosphine catalyst.The selectivity of the reaction depends on a nature and an amount of phosphine ligands.The reaction