256390-72-4

Upstream product

• 112-82-3 hexadecanyl bromide 
• 100-52-7 benzaldehyde 
• 256390-84-8 (S)-4-(hydroxymethyl)-2-phenyl-1,3-dioxane 

Downstream Products

• 916428-45-0 diethyl 3(S)-benzoyl-4-hexadecyloxy-1-butanephosphonate 
• 256390-77-9 C₄₈H₇₀O₆ 
• 256390-76-8 C₄₈H₇₂O₈S 
• 256390-89-3 C₄₈H₇₂O₆S 
• 256390-75-7 C₅₄H₇₄O₇S 

Relevant academic research and scientific papers

Synthesis and antitumor activity of ether glycero-phospholipids bearing a carbamate moiety at the sn-2 position: Selective sensitivity against prostate cancer cell lines

Analogues of 1-O-hexadecyl-sn-3-glycerophosphonocholine (compounds 1-4) or sn-3-glycerophosphocholine (compound 5) bearing a carbamate or dicarbamate moiety at the sn-2 position were synthesized and evaluated for their antiproliferative activity against c

SYNTHESIS OF GLYCEROLIPID CARBAMATES AND DICARBAMATES AND THEIR USE AS ANTITUMOR COMPOUNDS

The syntheses and in vitro antitumor properties of carbamate-containing, dicarbamate-containing, and ureido-containing phospholipid compounds that have an ether linkage at the C-1 position of a glycerol backbone, a carbamate, dicarbamate, or ureido moiety

Convergent C-glycolipid synthesis via the Ramberg-Baecklund reaction: active antiproliferative glycolipids.

[formula: see text] A novel methodology has been developed, employing the Ramberg-Baecklund rearrangement and ionic hydrogenation to synthesize C-glycosides with high stereoselectivity at the anomeric center. The C-glycolipid 14b exhibits antiproliferativ