354567-18-3

Upstream product

• 148407-40-3 (2R,3R)-3-undecyloxirane-2-methanol 
• 103773-79-1 [(2S,4S)-2-phenyl-1,3-dioxan-4-yl]methanol 
• 17049-50-2 n-decyl magnesium bromide 
• 79413-94-8 (2S,4S)-2-Phenyl-4-tosyloxymethyl-1,3-dioxan 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 139623-13-5 (R)-1,3-dihydroxytetradecane 

Downstream Products

• 139623-16-8 (R)-3-benzyloxy-1-hydroxytetradecane 
• 902769-93-1 (E)-(8S,10R)-10-Benzyloxy-henicos-6-en-8-ol 
• 902769-92-0 (E)-(8R,10R)-10-Benzyloxy-henicos-6-en-8-ol 
• 902770-00-7 (2S,3R)-2-((R)-2-Benzyloxy-tridecyl)-3-hexyl-2,3-dihydro-furan 
• 902769-91-9 (8S,10R)-10-Benzyloxy-henicos-6-yn-8-ol 
• 902769-90-8 (8R,10R)-10-Benzyloxy-henicos-6-yn-8-ol 
• 902769-99-7 (2S,3R)-2-((R)-2-Benzyloxy-tridecyl)-5-ethoxy-3-hexyl-tetrahydro-furan 
• 902769-98-6 {(R)-1-[(E)-(S)-2-(2-Bromo-1-ethoxy-ethoxy)-non-3-enyl]-dodecyloxymethyl}-benzene 
• 112763-97-0 (R)-3-phenylmethyloxy-tetradecanal 
• 137119-93-8 (R)-3-benzyloxy-1-(methanesulfonyloxy)tetradecane 
• 288402-93-7 (4aR,6S,7S,8R,8aS)-7-Amino-8-((R)-3-benzyloxy-tetradecyloxy)-2,2-dimethyl-hexahydro-pyrano[3,2-d][1,3]dioxine-6-carbonitrile 
• 288402-92-6 2,6-anhydro-3-azido-4-O-[(R)-3-(benzyloxy)tetradecyl]-3-deoxy-5,7-O-isopropylidene-D-glycero-D-ido-heptononitrile 
• 288402-89-1 allyl 2-azido-3-O-[(R)-3-(benzyloxy)tetradecyl]-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 288402-91-5 2,2,2-trichloroethylimidoyl 2-azido-3-O-[(R)-3-(benzyloxy)tetradecyl]-2-deoxy-4,6-O-isopropylidene-α-D-glucopyranoside 

Relevant academic research and scientific papers

Stereoselective synthesis of (-)-tetrahydrolipstatin via a radical cyclization based strategy

An efficient and flexible approach for the total synthesis of (-)-tetrahydrolipstatin is described. The main features of the synthetic strategy are a stereocontrolled radical cyclization and the successful utilization of commercially available S-malic acid.

Synthesis of GLA-60 type pyran carboxylic acids with an alkyl chain instead of an ester chain as LPS-antagonists

Synthesis of GLA-60 type pyran carboxylic acid analogues with an alkyl chain instead of an ester chain and their LPS-antagonist activity toward human U937 cells are described.