90129-51-4

Upstream product

• 76339-71-4 (2S,3R,5S)-2-methyl-5-(1-methylethenyl)-3-(phenylseleno)-cyclohexanone 
• 1666-13-3 diphenyl diselenide 

Downstream Products

• 97747-44-9 C₂₁H₃₀O₃Se 
• 97690-97-6 (1R,2R,5S)-2-methyl-5-(1-methylethenyl)-1-((tetrahydropyran-2-yl)oxy)-3-cyclohexene 
• 97747-41-6 (1R,2R,5S)-2-methyl-5-(1-methylethenyl)-3-cyclohexen-1-ol 
• 90129-47-8 (4S,5R)-4-hydroxy-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone 

Relevant academic research and scientific papers

Stereoselective synthesis of both half segments for (-)-sarcophytonin A and (-)-sarcophytoxide

A stereoselective synthesis of a dihydrofuran derivative (5) and an allylhalide (8), possible precursors of the cembranes (-)-sarcophytonin A and (-)-sarcophytoxide, is described. The optically active dihydrofuran, right half, segment (49) was synthesized

Highly Efficient Conversion of (-)-Carvone to (+)-5β-Hydroxycarvone

(-)-Carvone has been efficiently transformed into (+)-5β-hydroxycarvone (1), which is expected to play an important role as a potential precursor or as a chiral template in the synthesis of natural products.Both hydroxy selenides 4 and 5, obtained by the