87515-26-2

Upstream product

• 3386-33-2 1-chlorooctadecane 
• 1708-40-3 trans-2-phenyl-1,3-dioxan-5-ol 
• 76-84-6 triphenylmethyl alcohol 
• 82521-21-9 cis-5-(1-octadecyloxy)-2-phenyl-1,3-dioxan 
• 112-89-0 1-Bromooctadecane 
• 1708-40-3 2-phenyl-[1,3]dioxan-5-ol 
• 629-93-6 n-iodooctadecane 
• 1708-40-3 cis-5-hydroxyl-2-phenyl-1,3-dioxane 

Downstream Products

• 87515-29-5 (R,S)-3-brom-2-(1-octadecyloxy)propylbenzoat 

Relevant academic research and scientific papers

Anomeric O-alkylation, 15: New 2/1-type surfactants by anomeric O-alkylation of mannofuranose

New 2/1-type surfactants were synthesized from glycerol derivatives 2a-e having a long-chain 2-O-alkyl substituent. Transformation of 2a-d into 1,3-di-O-trifluoromethanesulfonates 4a-d and their use in anomeric O-alkylation of mannofuranose 7 afforded aft

1,3(R):4,6(R)-DI-O-BENZYLIDEN-D-MANNIT ALS AUSGANGSPRODUKT FUER DIE SYNTHESE OPTISCH AKTIVER GLYCERIN-DERIVATE

Starting from the di-O-benzylidene-D-mannitol derivative 11, certain types of optically active glycerol derivatives can be prepared with a minimum of protecting group chemistry.This is exemplified by an efficient synthesis of 2-O-alkyl glyceric acid derivatives 22 and 23.