864541-97-9

Upstream product

• 925-90-6 ethylmagnesium bromide 
• 215251-69-7 4-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methylbutanamide 
• 444068-99-9 2-(4-benzyloxyphenoxy)-4-(tert-butyldiphenylsilyloxy)-N-methoxy-N-methylbutyramide 
• 864541-96-8 4-(4-benzyloxyphenoxy)-6-(tert-butyldiphenylsilyloxy)hexan-3-one 
• 10467-10-4 ethylmagnesium iodide 

Downstream Products

• 1638110-65-2 (E)-ethyl 6-(tert-butyldiphenylsilyloxy)-3-ethylhex-2-enoate 
• 1638110-71-0 (Z)-ethyl 6-(tert-butyldiphenylsilyloxy)-3-ethylhex-2-enoate 

Relevant academic research and scientific papers

Preparation of precursors for the synthesis of analogues of rhazinilam

Rhazinilam a structurally relatively simple tetracyclic natural product exerts interesting anticancer activities in vitro, which are difficult to reproduce in vivo. Based on the findings accumulated during the synthetic efforts and on the known metabolic

Evaluation of a new linker system cleaved using samarium(II) iodide. Application in the solid phase synthesis of carbonyl compounds

A new linker design for solid phase synthesis has been developed that is cleaved under mild, neutral conditions using samarium(II) iodide. The feasibility of the linker approach has been illustrated in the solid phase synthesis of ketones and amides using

Diastereoselective ring-closing metathesis for the construction of a quaternary carbon stereogenic center

A diastereoselective ring-closing metathesis of the trienes 1 leading to the formation of a quaternary carbon stereogenic center on the cyclohexenes 2 has been developed.