113219-32-2

Upstream product

• 95851-64-2 6,7-epoxy-3,7-dimethyl-oct-2-enyl phenyl sulfide 

Downstream Products

• 95851-66-4 (E)-2,6-Dimethyl-8-phenylsulfanyl-octa-1,6-dien-3-ol 
• 95851-73-3 3-((3E,7E)-3,7-Dimethyl-9-phenylsulfanyl-nona-3,7-dienyl)-2-methyl-2-(4-methyl-pent-3-enyl)-oxirane 
• 95851-68-6 2-((3E,7E)-(1S,2S)-4,8-Dimethyl-2-phenylsulfanyl-cyclodeca-3,7-dienyl)-6-methyl-hept-5-en-2-ol 
• 95851-72-2 (1E,5E)-(7S,8S)-8-((E)-1,5-Dimethyl-hexa-1,4-dienyl)-1,5-dimethyl-7-phenylsulfanyl-cyclodeca-1,5-diene 
• 95851-69-7 (10E,14E)-6-Chloro-2,6,10,14-tetramethyl-16-phenylsulfanyl-hexadeca-2,10,14-trien-7-one 
• 95851-70-0 (1E,5E)-(7S,8S)-1,5-Dimethyl-8-(5-methyl-1-methylene-hex-4-enyl)-7-phenylsulfanyl-cyclodeca-1,5-diene 
• 95910-64-8 (+/-)-Biflora-4,10(19),15-triene 

Relevant academic research and scientific papers

SYNTHESIS OF MACROCYCLIC TERPENOIDS BY INTRAMOLECULAR CYCLIZATION IX. TOTAL SYNTHESIS OF (+/-)-OBSCURONATIN AND (+)-BIFLORA-4,10(19),15-TRIENE.

Stereoselective total synthesis of (+/-)-obscuronatin, a marine diterpene with a 10-membered ring, has been achieved utilizing the anion-induced cyclization of an acyclic epoxy sulfide.The synthesis confirmed the stereostructure of the natural product.