304678-71-5

Upstream product

• 36896-63-6 dimethylaluminium phenylthiolate 
• 304678-59-9 (E)-(S)-7-((S)-4-tert-Butyl-2-oxo-oxazolidin-3-yl)-3-methyl-7-oxo-hept-5-enal 
• 108-98-5 thiophenol 

Relevant academic research and scientific papers

Highly stereoselective and efficient synthesis of functionalized cyclohexanes with multiple stereocenters

Chiral 7-oxo-2-enimides 2, which were readily obtained through a silyloxy-Cope rearrangement of syn-aldol products 1, have proved to be versatile substrates for a one-step, highly efficient and stereoselective synthesis of functionalized cyclohexanes. Org

Domino Michael aldol and domino Michael Mannich reactions: Highly stereoselective synthesis of functionalized cyclohexanes

Enantiopure and highly functionalized cyclohexanes may be accessed in a single step and with stereocontrol from the 7-oxo-2-enimides 1 with use of the title reactions (see scheme). The bifunctional substrates 1 are available by a thermal [3.3]-sigmatropic