268736-28-3

Upstream product

• 16666-80-1 triphenylphosphonio-1-methylethanide 
• 268736-32-9 2-((2R,3S,5R)-3-methyl-5-{[(1R,2S)-2-phenylcyclohexyl]oxy}tetrahydro-2-furanyl)acetaldehyde 
• 268736-31-8 (2R,4S,5R)-4-methyl-5-(2-hydroxy-ethyl)tetrahydro-2-furanyl-(1R,2S)-2-phenylcyclohexyl ether 
• 268736-27-2 (2S,4S,5R)-4-methyl-5-vinyltetrahydro-2-fyranyl (1R,2S)-2-phenylcyclohexyl ether 

Downstream Products

• 98919-68-7 (1R,2S)-trans-2-phenylcyclohexanol 

Relevant academic research and scientific papers

Highly stereoselective radical cyclization of haloacetals controlled by the acetal center

A systematic investigation of radical haloacetal cyclizations (Ueno-Stork reaction) where the acetal center is the unique stereogenic element is reported. This highly diastereoselective reaction can be used for the preparation of polysubstituted tetrahydrofurans and γ-lactones. We report herein the full experimental details of reactions where up to three new chiral centers are created. To demonstrate the potential of this approach, short syntheses of (+)-eldanolide and of tricyclic acetals related to biologically active lignans have been achieved.

Desymmetrization of 1,4-dien-3-ols and related compounds via Ueno-Stork radical cyclizations

Desymmetrization of 1,4-dien-3-ols and related compounds via Ueno-Stork radical cyclizations is reported. The stereochemistry of the cyclization is controlled by the acetal center. Excellent stereocontrol at C(4) and C(5) of the newly formed tetrahydrofuran rings is observed. Use of a chiral auxiliary allows the preparation of enantiomerically pure material. The utility of this method has been demonstrated by achieving a short synthesis of (+)-eldanolide, the pheromone of the male African sugarcane stem borer Eldana saccharina.