955030-34-9

Upstream product

• 380909-82-0 (S)-4-Benzyl-3-[(2S,3R)-5-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2-methyl-pentanoyl]-oxazolidin-2-one 
• 112897-03-7 3-(tert-butyldiphenylsilyloxy)-1-propanal 
• 1415934-52-9 (2S,3R)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-5-(tert-butyldiphenylsilyloxy)-3-hydroxy-2-methylpentan-1-one 

Downstream Products

• 1415934-53-0 (4S,5R,6R)-8-(tert-butyldiphenylsilyloxy)-6-(4-methoxybenzyloxy)-5-methyloct-1-en-4-ol 
• 1415934-54-1 (4R,5R,6R)-8-(tert-butyldiphenylsilyloxy)-6-(4-methoxybenzyloxy)-5-methyloct-1-en-4-ol 
• 955030-37-2 C₅₆H₉₂O₇Si₃ 
• 955030-23-6 C₃₁H₄₀O₃Si 
• 955030-55-4 C₃₀H₃₈O₄Si 
• 955030-35-0 (2R,3R)-5-(tert-butyldiphenylsilyloxy)-3-(4-methoxybenzyloxy)-2-methylpentan-1-ol 
• 955030-51-0 tert-butyl(2-((4R,5R)-2-(4-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)ethoxy)diphenylsilanediol 

Relevant academic research and scientific papers

Iridium-catalyzed allylation of chiral β-stereogenic alcohols: Bypassing discrete formation of epimerizable aldehydes

The cyclometalated π-allyliridium 3,4-dinitro-C,O-benzoate complex modified by (R)- or (S)-Cl,MeO-BIPHEP promotes the transfer hydrogenative coupling of allyl acetate to β-stereogenic alcohols with good to excellent levels of catalyst-directed diastereose

A cross-metathesis approach for the synthesis of tedanolide and 13-deoxytedanolide: stereoselective synthesis of the C3-C16 segment

A unified synthetic strategy has been devised for the synthesis of both tedanolide and 13-deoxytedanolide, which involves a cross-metathesis reaction as the key step. We report herein the stereoselective synthesis of the C3-C16 segment (+)-5b and subseque

Stereoselective Aldol-Type Cyclization Reaction Mediated by Dibutylboron Triflate/Diisopropylethylamine

(Equation presented) Dibutylboron triflate/diisopropylethylamine mediated aldol-type cyclization provides an expedient route for the stereoselective synthesis of cyclic ethers in a single step. The method is highly efficient for the stereoselective synthe