862251-87-4

Upstream product

• 911285-64-8 C₃₂H₅₀O₁₃SSi 
• 911285-63-7 C₃₁H₄₈O₁₁Si 
• 911285-65-9 C₂₆H₃₆O₁₃S 
• 862251-82-9 C₂₅H₃₄O₁₁ 
• 911285-66-0 C₂₅H₃₂O₁₀ 
• 862251-84-1 C₂₅H₃₁BrO₁₀ 
• 862251-86-3 C₂₅H₃₂O₁₀ 
• 911285-62-6 C₃₄H₄₂O₁₄ 

Downstream Products

• 862251-88-5 Benzoic acid (1S,2S,3R,10R,11R,12R,15S)-11,12-diacetoxy-15-((2R,3S)-3-benzoylamino-2-hydroxy-3-phenyl-propionyloxy)-1-hydroxy-10,14,17,17-tetramethyl-4-oxo-6-oxa-tricyclo[11.3.1.0^3,10]heptadec-13-en-2-yl ester 
• 911285-72-8 (2R,4S,5R)-3-Benzoyl-2-(4-methoxy-phenyl)-4-phenyl-oxazolidine-5-carboxylic acid (1S,2S,3R,10R,11R,12R,15S)-11,12-diacetoxy-2-benzoyloxy-1-hydroxy-10,14,17,17-tetramethyl-4-oxo-6-oxa-tricyclo[11.3.1.0^3,10]heptadec-13-en-15-yl ester 

Relevant academic research and scientific papers

Synthesis, biology, and modeling of a C-4 carbonyl C,D-seco-taxoid

A C,D-seco-paclitaxel derivative 26 was prepared from taxine and tested for biological activity. Chemical reactivity of the seco-compounds proved to be substantially modified, with respects to taxoids. The corresponding C,D-seco-taxoid does not show tubul

Synthesis, biological evaluation, and modeling of a C,D-seco-taxoid

A C,D-seco-paclitaxel derivative 12 was prepared and tested for biological activity. The key step in the synthesis was a free radical fragmentation of the bicyclic tertiary alcohol 7 under the conditions of the hypobromite reaction. The compound 12 showed