111120-83-3

Upstream product

• 129313-31-1 (+/-)-(2S^*,3S^*)-2,3-Epoxy-2-methyl-3-phenylpropan-1-ol 
• 1504-55-8 (E)-3-phenyl-2-methyl-2-propenol 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 343771-16-4 (+/-)-(2R^*,3S^*)-2,3-Epoxy-2-methyl-3-phenylpropanal 
• 76638-09-0 (2R,3S)-2-methyl-3-phenyloxirane-2-carbaldehyde 

Downstream Products

• 118744-18-6 Ethyl (4R^*,5S^*)-5-hydroxy-4-methyl-5-phenylpentanoate 
• 122358-34-3 (4R^*,5S^*)-5-Hydroxy-4-methyl-5-phenylpentanoic acid 
• 91496-12-7 (+/-)-(5R^*,6S^*)-6-Phenyl-5-methyltetrahydropyran-2-one 
• 91496-12-7 (5S,6R)-5-Methyl-6-phenyl-tetrahydro-pyran-2-one 
• 111120-84-4 Ethyl (+/-)-(E)-(4R^*,5S^*)-5-hydroxy-4-methyl-5-phenyl-2-pentenoate 
• 122358-29-6 Ethyl (E)-5-hydroxy-4-methyl-5-phenyl-3-pentenoate 
• 122358-31-0 Ethyl (E)-4-methyl-5-oxo-5-phenyl-3-pentenoate 
• 122358-30-9 Ethyl (E)-5-hydroxy-4-methylene-5-phenyl-2-pentenoate 
• 122358-32-1 Ethyl (E)-4-(formyloxy)-5-hydroxy-4-methyl-5-phenyl-2-pentenoate 
• 914366-90-8 Ethyl (4S,5S)-5-hydroxy-4-methyl-5-phenyl-2-pentenoate 

Relevant academic research and scientific papers

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