1448461-33-3

Upstream product

• 842125-04-6 (E)-4-((4-methoxybenzyl)oxy)but-2-en-1-al 
• 688317-98-8 trans-carbonic acid methyl ester pent-2-enyl ester 
• 1448461-17-3 1-({[(2E,4E,6S)-6-ethylocta-2,4,7-trien-1-yl]oxy}methyl)-4-methoxybenzene 
• 126983-28-6 (E)-3-bromoacrylate of (R)-pantolactone 
• 1448461-10-6 5-{[(2S)-2-ethylbut-3-en-1-yl]sulfonyl}-1-phenyl-1H-tetrazole 

Relevant academic research and scientific papers

Syntheses of the hexahydroindene cores of indanomycin and stawamycin by combinations of iridium-catalyzed asymmetric allylic alkylations and intramolecular diels-alder reactions

Short and concise syntheses of the hexahydroindene cores of the antibiotics indanomycin (X-14547 A) and stawamycin are presented. Key methods used are an asymmetric iridium-catalyzed allylic alkylation, a modified Julia olefination, a Suzuki-Miyaura coupling, and an intramolecular Diels-Alder reaction.