1448461-16-2

Upstream product

• 845734-51-2 5-{[(2S)-2-methylbut-3-en-1-yl]sulfonyl}-1-phenyl-1H-tetrazole 
• 842125-04-6 (E)-4-((4-methoxybenzyl)oxy)but-2-en-1-al 

Downstream Products

• 1448461-32-2 (3R)-4,4-dimethyl-2-oxotetrahydrofuran-3-yl (2E,6S,7E,9E)-11-({[4-(methoxyphenyl)]methoxy})-6-methylundeca-2,7,9-trienoate 
• 1448461-19-5 methyl (2E,6S,7E,9E)-6-methyl-11-({[4-(methyloxy)phenyl]methyl}oxy)undeca-2,7,9-trienoate 

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.