97691-00-4

Upstream product

• 1666-13-3 diphenyl diselenide 
• 76339-71-4 (2S,3R,5S)-2-methyl-5-(1-methylethenyl)-3-(phenylseleno)-cyclohexanone 
• 110-87-2 3,4-dihydro-2H-pyran 
• 90056-25-0 (1S,2S,3R,5S)-2-methyl-5-(1-methylethenyl)-3-(phenylseleno)-cyclohexanol 

Downstream Products

• 138944-97-5 (1S,2R,5S)-5-(1-hydroxypropan-2-yl)-2-methyl-3-cyclohexenol tetrahydropyranyl ether 
• 138945-09-2 (1S,2R,5S)-7,8-epoxy-2,7-dimethyl-1-(tetrahydropyranyl)oxy-3-cyclohexene 
• 97691-01-5 C₂₁H₃₀O₃Se 
• 90129-47-8 (4S,5R)-4-hydroxy-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enone 
• 97805-15-7 (1S,2R,5S)-2-methyl-5-(1-methylethenyl)-3-cyclohexen-1-ol 
• 90056-26-1 (1S,2R,5S)-2-methyl-5-(1-methylethenyl)-1-((tetrahydropyran-2-yl)oxy)-3-cyclohexene 
• 138945-06-9 (2R,3R,4S)-3-formyl-2-<2-(methoxycarbonyl)propyl>-4-methyl-3-phenylseleneo-tetrahydrofuran 
• 138945-06-9 (2R,3S,4S)-3-formyl-2-<2-(methoxycarbonyl)propyl>-4-methyl-3-phenylseleneo-tetrahydrofuran 
• 138945-06-9 3-((2R,4R)-3-Formyl-4-methyl-3-phenylselanyl-tetrahydro-furan-2-yl)-2-methyl-propionic acid methyl ester 
• 138945-54-7 (1R,3S,4S,5S,6S,9S)-3-hydroxy-4,9-dimethyl-5-phenylseleno-7-oxabicyclo<4.3.0>nonane 
• 138945-37-6 (1R,3S,4S,5S,6S,9R)-3-hydroxy-4,9-dimethyl-5-phenylseleno-7-oxabicyclo<4.3.0>nonane 
• 138945-23-0 (2R)-3-<(tert-butyldimethylsilyl)oxymethyl>-2-<2-(methoxycarbonyl)-2-phenylselenopropyl>-4-methyl-2,5-dihydrofuran 
• 138944-98-6 (1R,3S,4S,5S,6S,9R)-4,9-dimethyl-5-phenylseleno-3-(tetrahydropyran-2-yloxy)-7-oxabicyclo<4.3.0>nonane and (1R,3S,4S,5S,6S,9S)-4,9-dimethyl-5-phenylseleneo-3-(tetrahydropyran-2-yloxy)-7-oxabicyclo<4.3.0>nonane 

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