512780-95-9

Upstream product

• 512780-89-1 Benzoic acid (1S,2S,3R,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-4-hydroxymethyl-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-tricyclo[9.3.1.0^3,8]pentadec-4-en-2-yl ester 
• 512780-88-0 Benzoic acid (1S,2S,3R,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-4-trimethylsilanyloxymethyl-tricyclo[9.3.1.0^3,8]pentadec-4-en-2-yl ester 
• 512780-87-9 C₄₀H₅₄O₉Si 

Downstream Products

• 512780-97-1 Benzoic acid (1S,2S,3R,5S,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1,5-dihydroxy-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-4-methylene-9,14-dioxo-tricyclo[9.3.1.0^3,8]pentadec-2-yl ester 
• 512781-00-9 Benzoic acid (1S,2S,3R,4S,5S,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1,4,5-trihydroxy-4-hydroxymethyl-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-tricyclo[9.3.1.0^3,8]pentadec-2-yl ester 
• 512781-05-4 Benzoic acid (1S,2S,3R,4S,5S,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1,4-dihydroxy-4-hydroxymethyl-5-methanesulfonyloxy-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-tricyclo[9.3.1.0^3,8]pentadec-2-yl ester 
• 512781-02-1 Benzoic acid (1S,2S,3R,4S,5S,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1,4,5-trihydroxy-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-4-trimethylsilanyloxymethyl-tricyclo[9.3.1.0^3,8]pentadec-2-yl ester 
• 512781-04-3 Benzoic acid (1S,2S,3R,4S,5S,7S,8S,10R,11S)-7-(tert-butyl-dimethyl-silanyloxy)-1,4-dihydroxy-5-methanesulfonyloxy-10-(4-methoxy-benzyloxy)-8,15,15-trimethyl-9,14-dioxo-4-trimethylsilanyloxymethyl-tricyclo[9.3.1.0^3,8]pentadec-2-yl ester 

Relevant academic research and scientific papers

Chemical modification of a highly functionalized taxane. The consequences of an absent bridgehead double bond on oxetane D-ring construction

An oxetane D-ring has been fused to the framework of the highly functionalized taxane 2. The synthetic route is based on a trimethylsilyl triflate-promoted epoxide-opening step, followed by stereocontrolled, regioreversed oxirane formation and reductive t