144993-60-2

Upstream product

• 107-21-1 ethylene glycol 
• 144936-88-9 4-<3-Oxo-8-(2',2',2'-trichloroethylcarbonoyl)-4-E-nonen>-2,5-diphenyloxazole 
• 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 
• 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 
• 144763-00-8 4-(3-Dioxolan-8-hydroxy-5-E-nonen)-2,5-diphenyloxazole 
• 2549-30-6 4-Methyl-2,5-diphenyloxazole N-oxide 
• 4630-06-2 6-methylhept-5-en-2-ol 

Downstream Products

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

Relevant academic research and scientific papers

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

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