954096-32-3

Upstream product

• 810682-39-4 (S)-3-(Bromomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-12-3 (S)-3-(Chloromethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 87655-21-8 (S)-3-hydroxy-2,2-dimethylcyclohexanone 
• 810682-53-2 (S)-3-(Iodomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-13-4 (1S,5S)-3,3,9,9-Tetramethyl-2-oxa-3-sila-bicyclo[3.3.1]nonan-5-ol 

Downstream Products

• 810682-44-1 Acetic acid (S)-4-(4-methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-45-2 [(S)-4-(4-Methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enyl]-methanol 
• 810682-17-8 Acetic acid (S)-1-hydroxy-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-43-0 (S)-1-Hydroxymethyl-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enol 
• 810682-16-7 (S)-8-(4-Methoxy-benzyloxymethyl)-2,2,6,6-tetramethyl-1,3-dioxa-spiro[4.5]dec-7-ene 
• 810682-41-8 (S)-2,2,6,6-Tetramethyl-8-methylene-1,3-dioxa-spiro[4.5]decan-7-one 
• 810682-15-6 (S)-2,2,6,6-Tetramethyl-8-methylene-1,3-dioxa-spiro[4.5]decan-7-ol 
• 810682-46-3 (S)-1-Hydroxymethyl-3-iodo-2,2,4-trimethyl-cyclohex-3-enol 
• 810682-18-9 (S)-2,2,6,6,8-Pentamethyl-1,3-dioxa-spiro[4.5]decan-7-one 
• 954096-34-5 C₁₇H₂₁IO₂ 
• 954096-33-4 C₁₇H₂₁IO₂ 
• 954096-40-3 C₃₄H₄₃IO₄ 
• 954096-37-8 C₃₄H₄₀INO₃ 
• 954096-36-7 C₃₃H₃₉IO₃ 

Relevant academic research and scientific papers

Construction of the taxane skeleton via the stereoselective conjugate addition of cyanide and the intramolecular B-alkyl Suzuki-Miyaura coupling reaction

Construction of the taxane skeleton via the stereoselective conjugate addition of cyanide and the intramolecular B-alkyl Suzuki-Miyaura coupling reaction is described. A conjugate addition of cyanide to enone 17 proceeded diastereoselectively to provide t

Development of silicon-tethered anionic reaction and its application to the synthesis of chiral A-ring moieties of Taxol

Silicon-tethered intramolecular nucleophilic additions of a hydroxymethyl unit to ketones in β-hydroxyketones have been developed. The product obtained by this protocol was successfully converted to chiral A-ring moieties of Taxol. Also developed was a pr