312923-92-5

Upstream product

• 312923-90-3 (1S,3R,7R,8S,9R,10S,11S)-9-Benzyloxymethyl-10-hydroxymethyl-11-methyl-7-trimethylsilanyloxy-4-oxa-tricyclo[5.3.1.0^3,8]undecan-5-one 
• 312923-94-7 C₂₀H₂₂O₅C₃H₉SiI 

Downstream Products

• 814920-12-2 C₂₇H₃₆O₇ 
• 814920-13-3 C₂₈H₃₈O₆ 
• 814920-11-1 C₂₇H₃₈O₇ 
• 814919-99-8 C₂₈H₄₂O₇Si 
• 814920-14-4 C₂₈H₄₀O₇ 
• 814920-08-6 C₂₉H₄₂O₇Si 
• 814919-97-6 (1S,3R,7S,8S,9R,10R)-9-Benzyloxymethyl-10-(2-trimethylsilanyl-ethoxymethoxymethyl)-7-trimethylsilanyloxy-4-oxa-tricyclo[5.3.1.0^3,8]undecane-5,11-dione 
• 814920-02-0 C₃₀H₄₄O₇Si 
• 814920-09-7 C₂₉H₄₄O₇Si 
• 814920-00-8 C₃₁H₄₆O₇Si 
• 814920-01-9 C₃₀H₄₆O₈Si 
• 814920-07-5 C₃₀H₄₄O₉Si 
• 814919-96-5 C₃₃H₅₁BrO₈Si 
• 814920-26-8 (S)-2-[(1R,2S,6R,7S,8R,9R)-9-Benzyloxymethyl-4,4-dimethyl-10-oxo-8-(2-trimethylsilanyl-ethoxymethoxymethyl)-3,5-dioxa-tricyclo[5.2.2.0^2,6]undec-2-yl]-3-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde 

Relevant academic research and scientific papers

Studies on the total synthesis of (-)-CP-263,114

Alkoxyl radicals have a wide range of applications in organic synthesis due to their remarkable chemical properties in molecular transformation. The present study shows two types of alkoxyl radicals (primary vs tertiary) to selectively undergo dehydrogena

Asymmetric synthesis of the core structure of (-)-CP-263,114.

The enantioselective construction of a fully functionalized core structure of (-)-CP-263,114 (1), containing most of the required functionality for total synthesis, was conducted through sequential radical fragmentation-reductive olefination.