1445989-91-2

Upstream product

• 1445989-88-7 C₂₆H₃₉NO₂S₂Si 
• 1445989-89-8 (R,E)-3-(tert-butyldimethylsilyloxy)-6-methylnona-6,8-dienal 
• 790661-41-5 (S)-1-(4-benzyl-2-thioxothiazolidin-3-yl)ethan-1-one 
• 5390-04-5 pent-1-yn-5-ol 
• 104846-46-0 (4E)-5-iodo-4-methylpent-4-en-1-ol 
• 113375-54-5 (4E)-4-Methylhepta-4,6-dien-1-ol 
• 139026-03-2 (E)-4-Methyl-4,6-heptadienal 
• 1445989-80-9 (3R,6E)-1-((4R)-4-benzyl-2-thioxothiazolidin-3-yl)-3-hydroxy-6-methylnona-6,8-dien-1-one 

Relevant academic research and scientific papers

Stereoselective total synthesis of ieodomycins A and B and revision of the NMR spectroscopic data of ieodomycin B

Stereoselective total synthesis of antimicrobial marine metabolites ieodomycin A and B have been accomplished starting from commercially available 4-pentyn-1-ol featuring strategic application of the Negishi reaction, Kumada coupling, and Crimmins acetate aldol. This revises the proton NMR spectra of ieodomycin B.