1290537-64-2

Upstream product

• 1290537-63-1 (3R,3'R)-4,4'-((4R,6R)-2,2-dimethyl-1,3-dioxane-4,6-diyl)bis(3-((tert-butyldiphenylsilyl)oxy)butan-1-ol) 
• 3282-30-2 pivaloyl chloride 
• 1290537-62-0 (((2R,2'R)-((4R,6R)-2,2-dimethyl-1,3-dioxane-4,6-diyl)bis(pent-4-ene-2,1-diyl))bis(oxy))bis(tertbutyldiphenylsilane) 
• 1182723-08-5 (2R,2'R)-1,1'-((4S,6S)-dimethyl-1,3-dioxane-4,6-diyl)dipent-4-en-2-ol 

Downstream Products

• 1290537-67-5 (R)-3-((tert-butyldiphenylsilyl)oxy)-4-((4R,6R)-6-((S)-2-((tert-butyldiphenylsilyl)oxy)but-3-en-1-yl)-2,2-dimethyl-1,3-dioxan-4-yl)butyl pivalate 
• 1290537-66-4 (R)-3-((tert-butyldiphenylsilyl)oxy)-4-((4R,6R)-6-((S)-2-((tert-butyldiphenylsilyl)oxy)-4-((2-nitrophenyl)selanyl)butyl)-2,2-dimethyl-1,3-dioxan-4-yl)butyl pivalate 

Relevant academic research and scientific papers

C(21)-C(40) of tetrafibricin via metal catalysis: Beyond stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles

Chemical equations presented. The C(21)-C(40) fragment of fibrinogen receptor inhibitor tetrafibricin was prepared in 12 steps from propane diol (longest linear sequence). In this approach, 6 C-C bonds are formed via asymmetric iridium catalyzed transfer