723340-75-8

Upstream product

• 108-05-4 vinyl acetate 
• 83333-75-9 (E)-2-phenylpent-3-en-2-ol 
• 108-24-7 acetic anhydride 
• 124006-49-1 (2R,3E)-4-phenyl-3-penten-2-ol 
• 536-74-3 phenylacetylene 
• 98-86-2 acetophenone 
• 6712-32-9 2-phenyl-3-pentyn-2-ol 
• 285566-28-1 (3E)-4-phenyl-3-penten-2-ol 

Downstream Products

• 1592890-25-9 (E)-(4-methylhepta-1,5-dien-4-yl)benzene 
• 1592890-27-1 (E)-(4-methylhepta-2,6-dien-2-yl)benzene 
• 54758-36-0 1-methyl-1-phenyl-1,3-butadiene 
• 1608-27-1 1-phenylpenta-1,3-diene 
• 723341-08-0 (2S,4S)-2-methyl-2-phenylpentan-1,4-diol 1-acetate 
• 723340-76-9 (3R,4E)-3-methyl-3-phenylhex-4-enoic acid 
• 723340-97-4 (2S,4S)-2-methyl-2-phenylpentane-1,4-diol 
• 723340-77-0 (4R,5E)-4-methyl-4-phenylhept-5-en-2-one 
• 99343-90-5 (2R,4S)-tetrahydro-2,4-dimethyl-4-phenylfuran 
• 99343-90-5 (2S,4S)-tetrahydro-2,4-dimethyl-4-phenylfuran 

Relevant academic research and scientific papers

Catalytic stereospecific allyl-allyl cross-coupling of internal allyl electrophiles with allylB(pin)

Application of internal electrophiles in catalytic stereospecific allyl-allyl cross-coupling enable the rapid construction of multisubstituted 1,5-dienes, including those with all carbon quaternary centers. Compounds with minimal steric differentiation ca

A mesoporous-silica-immobilized oxovanadium cocatalyst for the lipase-catalyzed dynamic kinetic resolution of racemic alcohols

V for resolution: A new oxovanadium catalyst (V-MPS; see scheme) immobilized in the pores of mesoporous silica has been developed. The combined use of V-MPS and lipases achieved the dynamic kinetic resolution of a wide range of racemic alcohols (1 or 2) t

One-pot synthesis of optically active allyl esters via lipase-vanadium combo catalysis

The combination of vanadium-oxo compounds (3 or 4) with a lipase produced the regio- and enantioconvergent transformation of racemic allyl alcohols (1 or 2) into optically active allyl esters. In this system, the vanadium compounds catalyzed the continuous racemization of the alcohols along with the transposition of the hydroxyl group, while the lipase effected the chemo- and enantioselective esterification to achieve the dynamic kinetic resolution.

Preparation of the Enantiomerically Enriched Isomers of the Odorous Cyclic Ethers Clarycet, Florol, and Rhubafuran by Enzymatic Catalysis

All the enantiomerically enriched stereoisomers of Clarycet (1), Florol (2), and Rhubafuran (3) were prepared by biocatalysis routes. Their absolute configurations were established, and their olfactory properties were fully evaluated.