144993-60-2

Upstream product

• 2549-33-9 4-(chloromethyl)-2,5-diphenyloxazole 
• 144993-59-9 4-<3-Dioxolan-8-(2',2',2'-trichloroethylcarbonoyl)-5-E-nonen>-2,5-diphenyloxazole 
• 144936-88-9 4-<3-Oxo-8-(2',2',2'-trichloroethylcarbonoyl)-4-E-nonen>-2,5-diphenyloxazole 
• 144762-97-0 4-(4-Triphenylphosphoranylidene-3-butanon)-2,5-diphenyloxazole 
• 144936-87-8 2-(2',2',2'-Trichloroethylcarbonoyl)-6-methyl-5-heptene 
• 144762-96-9 4-(2',2',2'-Trichloroethylcarbonoyl)pentanal 
• 2549-30-6 4-Methyl-2,5-diphenyloxazole N-oxide 
• 4630-06-2 6-methylhept-5-en-2-ol 
• 144763-00-8 4-(3-Dioxolan-8-hydroxy-5-E-nonen)-2,5-diphenyloxazole 
• 107-21-1 ethylene glycol 

Downstream Products

• 76353-69-0 (+/-)-Pyrenolide C 
• 144763-04-2 Z-2-Phenylselenyl-4-oxo-6-decen-9-olide 
• 144763-04-2 E-2-Phenylselenyl-4-oxo-6-decen-9-olide 
• 144763-03-1 2-Phenylselenyl-4-dioxolan-6-decen-9-olide 

Relevant academic research and scientific papers

The Synthesis of (+/-)-Pyrenolide C Using the Oxazole-Singlet Oxygen Reaction. Assignment of Stereochemistry.

Pyrenolide C has been synthesized for the first time using an oxazole template to construct the framework of the ten-membered unsaturated lactone system.The stereochemical assignment, based on the mode of synthesis, has been confirmed by NMR studies. Key

The Singlet Oxygen Conversion of Oxazoles to Triamides. Application in the Synthesis of (+/-)-Pyrenolide C. Assignment of Stereochemistry.

Pyrenolide C has been synthesized for the first time using an oxazole template to construct the framework of the ten-membered unsaturated lactone system.The stereochemical assignment of the allylic alcohol substituent, based on the mode of synthesis, has