856433-57-3

Upstream product

• 3536-96-7 vinylmagnesium chloride 

Downstream Products

• 856433-70-0 (4R,5S)-4-[(R)-2-(4-Methoxy-benzyloxy)-1-methyl-ethyl]-2,2-dimethyl-5-vinyl-[1,3]dioxane 
• 856433-58-4 (4R,5S)-4-[(R)-2-(4-Methoxy-benzyloxy)-1-methyl-ethyl]-2,2-dimethyl-[1,3]dioxane-5-carbaldehyde 
• 856433-59-5 (E)-3-{(4R,5S)-4-[(R)-2-(4-Methoxy-benzyloxy)-1-methyl-ethyl]-2,2-dimethyl-[1,3]dioxan-5-yl}-2-methyl-prop-2-en-1-ol 
• 856433-71-1 (E)-3-{(4R,5S)-4-[(R)-2-(4-Methoxy-benzyloxy)-1-methyl-ethyl]-2,2-dimethyl-[1,3]dioxan-5-yl}-2-methyl-acrylic acid ethyl ester 
• 856433-61-9 (Z)-3-((2S,3S)-3-{(4R,5S)-4-[(R)-2-(4-Methoxy-benzyloxy)-1-methyl-ethyl]-2,2-dimethyl-[1,3]dioxan-5-yl}-2-methyl-oxiranyl)-acrylic acid ethyl ester 

Relevant academic research and scientific papers

Synthetic studies of tedanolide, a marine macrolide displaying potent antitumor activity. Stereoselective synthesis of the C(13)-C(23) segment

(Chemical Equation Presented) A highly stereoselective synthesis of the C(13)-C(23) segment of tedanolide (1), an 18-membered macrolide isolated from the Caribbean sponge Tedania ignis, displaying significant cytotoxicity against KB and PS tumor cell line