949087-71-2

Upstream product

• 942513-97-5 (R)-2-(prop-2-ynyl)hex-5-en-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 942513-96-4 (4S)-4-benzyl-3-((R)-2-(prop-2-ynyl)hex-5-enoyl)oxazolidin-2-one 
• 1577-22-6 5-hexenoic acid 
• 134916-00-0 (4S)-4-benzyl-3-(hex-5-enoyl)-1,3-oxazolidin-2-one 

Downstream Products

• 949087-72-3 (R)-(3-vinylcyclohex-3-enyl)methyl 4-methylbenzenesulfonamide 
• 130548-10-6 (+)-rubiginone B2 
• 28882-53-3 (S)-8-hydroxy-3-methyl-3,4-dihydrotetraphene-1,7,12(2H)-trione 
• 681001-31-0 (R)-5-methyl-1-vinylcyclohex-1-ene 
• 681001-30-9 (R)-8-hydroxy-3-methyl-1,2,3,4-tetrahydrobenz[a]anthracene-7,12-dione 

Relevant academic research and scientific papers

Angucyclinone antibiotics: Total syntheses of YM-181741, (+)-ochromycinone, (+)-rubiginone B2, (-)-tetrangomycin, and MM-47755

(Chemical Equation Presented) A concise and highly enantioselective route has been developed for the synthesis of angucyclinone-type natural products. Utilizing this strategy, total syntheses of five natural products YM-181741, (+)-ochromycinone, (+)-rubi