93676-55-2

Upstream product

• 87164-37-2 hexahydro-3aα,4,5,6,7,7aα (3H) iodo-5β trimethyl-4,4,7a benzofurannone-2 
• 79693-70-2 tetrahydro-3aα,4,7,7aα (3H) trimethyl-4,4,7a benzofurannone-2 
• 87164-39-4 bromo-5α hexahydro-3aα,4,5,6,7,7aα (3H) hydroxy-6 trimethyl-4,4,7α benzofurannone-2 
• 459-85-8 (E)-4,8-dimethylnona-3,7-dienoic acid 
• 1133-01-3 hexahydro-3aα,4,5,6,7,7aα (3H) hydroxy-6 trimethyl-4,4,7α benzofurannone-2 
• 87164-34-9 hexahydro-3aα,4,5,6,7,7aα (3H) phenylseleno-3-tetrahydropyrannoxy-6 trimethyl-4,4,7a benzofurannone-2 
• 87164-41-8 hexahydro-3aα,4,5,6,7,7aα (3H) tetrahydropyrannoxy-6 trimethyl-4,4,7a benzofurannone-2 

Downstream Products

• 1133-03-5 (+/-)-loliolide 

Relevant academic research and scientific papers

Syntheese du (+/-)-loliolide ou hydroxy-6 teetrahydro-5,6,7,7a trimeethyl-4,4,7a(4H) benzofurannone-2 (6S,7aR) par cyclisation de l'acide homogeeranique

Starting from pure homogeranic acid 2, in a stereoselective fashion, we describe a new synthesis of (+/-)-loliolide 1.Cyclization of 2 with mercury trifluoroacetate or phenylselenyl chloride provides the isohydroactinidiolide 6 which was converted to the