519013-64-0

Upstream product

• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 233666-22-3 1-O-tert-butyldimethylsilyl-2-O-methanesulfonyloxy-ethane 
• 86864-60-0 2-(tert-butyldimethylsilyloxy)ethyl bromide 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 102229-10-7 2-(tert-butyldimethylsilyloxy)ethanol 

Downstream Products

• 160805-54-9 (E)-tert-butyldimethyl((5-phenylpent-2-en-1-yl)oxy)silane 
• 100009-29-8 (E)-1-tert-butyldimethylsilyloxy-3-phenyl-2-propene 
• 128741-83-3 (cis)-1-benzyloxy-4-(tert-butyldimethyl)silyloxy-2-butene 
• 151359-19-2 (E)-1-(Benzyloxy)-4-<(tert-butyldimethylsilyl)oxy>-2-butene 
• 141023-05-4 tert-Butyl-((E)-3-cyclohexyl-allyloxy)-dimethyl-silane 
• 874739-59-0 tert-butyldimethyl(((2E,4E)-5-phenylpenta-2,4-dien-1-yl)oxy)silane 
• 519013-65-1 5-[(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)sulfonyl]-1-phenyl-1H-tetrazole 

Relevant academic research and scientific papers

COMPOUND HAVING EP2 AGONISTIC ACTIVITY

Provided is an EP2 agonist having excellent safety. A compound represented by general formula (I) (wherein all symbols are as defined in the description), a salt or N-oxide of the compound, or a solvate or prodrug of the compound or the salt or N-oxide ha

Efficient and stereoselective synthesis of allylic ethers and alcohols

(Chemical Equation Presented) A short and efficient synthesis of allylic TBS ethers and allylic alcohols has been developed, based upon a unique Kocienski-Julia olefination reaction. Allylic alcohols and allylic ethers are obtained in good to excellent yields and with high (E)-selectivity. The conditions are mild and the procedure is broadly applicable.