178246-83-8

Upstream product

• 178246-79-2 α-benzyl-ω-[(tert-butyl)diphenylsilyloxy]bis[(R)-oxy(3-methyl)-1-oxopropane-1,3-diyl] 
• 178246-81-6 (R)-3-(tert-Butyl-diphenyl-silanyloxy)-butyric acid (R)-2-carboxy-1-methyl-ethyl ester 
• 178246-78-1 (R)-3-(tert-Butyldiphenylsilanyloxy)butyric acid methyl ester 
• 147963-64-2 (R)-3-[(tert-butyl)diphenylsilyloxy]butanoic acid 
• 101515-40-6 (R)-(-)-2-benzyloxycarbonyl-1-methylethyl (R)-(-)-3-hydroxybutyrate 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 178246-82-7 (R)-3-(tert-Butyl-diphenyl-silanyloxy)-butyric acid (R)-2-[(R)-2-((R)-2-benzyloxycarbonyl-1-methyl-ethoxycarbonyl)-1-methyl-ethoxycarbonyl]-1-methyl-ethyl ester 

Downstream Products

• 178246-84-9 α-Benzyl-ω-[(tert-butyl)diphenylsilyloxy]octa[(R)-oxy(3-methyl-1-oxopropan-1,3-diyl)] 
• 178246-85-0 C₄₈H₆₈O₁₇Si 
• 193953-30-9 3,5-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-benzoic acid (R)-2-((R)-2-{(R)-2-[(R)-2-(9H-fluoren-9-ylmethoxycarbonyl)-1-methyl-ethoxycarbonyl]-1-methyl-ethoxycarbonyl}-1-methyl-ethoxycarbonyl)-1-methyl-ethyl ester 
• 193953-12-7 (R)-3-(tert-Butyl-diphenyl-silanyloxy)-butyric acid (R)-2-{(R)-2-[(R)-2-(9H-fluoren-9-ylmethoxycarbonyl)-1-methyl-ethoxycarbonyl]-1-methyl-ethoxycarbonyl}-1-methyl-ethyl ester 
• 193953-33-2 3,5-Bis-hydroxymethyl-benzoic acid (R)-2-((R)-2-{(R)-2-[(R)-2-(9H-fluoren-9-ylmethoxycarbonyl)-1-methyl-ethoxycarbonyl]-1-methyl-ethoxycarbonyl}-1-methyl-ethoxycarbonyl)-1-methyl-ethyl ester 
• 819852-32-9 (5R,9R,13R,17R,21S)-2,2,5,9,13,17-hexamethyl-7,11,15,19-tetraoxo-3,3-diphenyl-21-(trifluoromethyl)-4,8,12,16,20-pentaoxa-3-silatricosan-23-oic acid benzyl ester 
• 819852-34-1 (5R,9R,13R,17R,21S)-2,2,5,9,13,17-hexamethyl-7,11,15,19-tetraoxo-3,3-diphenyl-21-(trifluoromethyl)-4,8,12,16,20-pentaoxa-3-silatricosan-23-oic acid 

Relevant academic research and scientific papers

On the structure of PHB (=Poly[(R)-3-hydroxybutanoic acid]) in phospholipid bilayers: Preparation of trifluoromethyl-labeled oligo[(R)-3-hydroxybutanoic acid] derivatives

Oligomers of (R)-3-hydroxybutanoate (OHB) have previously been shown to transport cations through lipid bilayers. The ion-transport activity has been attributed to the formation of hydrophobic aggregates or pores, which have been identified by fluorescenc

Monodisperse linear and cyclic oligo[(R)-3-hydroxybutanoates] containing up to 128 monomeric units

Using benzyl ester/(tert-butyl)diphenylsilyl ether protection, (COCl)2/pyridine esterification conditions, and a fragment-coupling strategy (with H2/Pd-C debenzylation and HF-pyridine desilylation), linear oligomers of (R)-3-hydroxyb