159099-82-8

Upstream product

• 14398-34-6 4-(3-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 79-77-6 (E)-β-ionone 
• 74345-31-6 2,4,4-trimethyl-3-(3-oxobut-1-enyl)cyclohex-2-enyl acetate 
• 84817-80-1 trans-4-bromo-β-ionone 

Downstream Products

• 937391-73-6 ethyl (+/-)-(2E,4E)-5-[1-(3-[(1,1-dimethylethyl)dimethylsilyloxy]-2,6,6-trimethyl-1-cyclohexen-1-yl)]-3-methyl-2,4-pentadienoate 
• 63184-94-1 1-(2,6,6-Trimethyl-3-oxo-1-cyclohexen-1-yl)-3-methyl-5-bromo-penta-1,3-diene 
• 879207-46-2 ethyl 13,14-dihydro-4-oxoretinoate 
• 29538-78-1 (2E,4E)-3-methyl-5-(2,6,6-trimethyl-3-oxo-1-cyclohexen-1-yl)-2,4-pentadienol 
• 63184-93-0 (2E,4E)-<5-(2,6,6-trimethyl-3-oxo-1-cyclohexen-1-yl)-3-methyl-2,4-pentadien-1-yl>triphenylphosphonium bromide 
• 1198339-71-7 C₂₀H₃₆OSi 

Relevant academic research and scientific papers

The location of the chromophore in rhodopsin: A photoaffinity study

A photoreactive analog of 11-cis-retinal was synthesized and used in photo-cross-linking studies to determine the orientation of the chromophore in bovine rhodopsin. The photoaffinity analog incorporated a tritium in the aldehyde group, a photoactivable d

A convenient cross-metathesis approach to trisporins

Three series of trisporins have been prepared using a strategy in which a cross-metathesis is the key step. This reaction has proved to be highly regioselective, allowing the combination of α- or β-ionone derivatives having a 1,1-disustituted olefin with

All-Trans-Retinol: All-Trans-13,14-Dihydroretinol Saturase and Methods of Its Use

Compositions of all-trans-retinol: all-trans-13,14-dihydroretinal saturase and methods of use thereof are provided.

Approaches to the synthesis of arisugacin A

Approaches to the synthesis of the important acetylcholinesterase inhibitor, arisugacin A, are described. Two different routes to?the key AB ring system are described: the first utilizes an intramolecular Diels-Alder reaction on a furan substrate and the