1314093-89-4

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 26153-38-8 3,5-dihydroxybenzaldehyde 
• 1314093-86-1 C₂₆H₂₆F₃NO₅ 
• 1314093-99-6 1,3-bis(4-methoxybenzyloxy)-5-[(E)-2-nitroethenyl]benzene 
• 1314093-97-4 3,5-bis(4-methoxybenzyloxy)benzaldehyde 

Downstream Products

• 1314093-93-0 1,3-bis(4-methoxybenzyloxy)-6-[(Z)-3-hydroxyprop-1-enyl]5-[2-(trifluoroacetamido)ethyl]benzene 
• 1314093-80-5 (+)-(S)-6,8-bis-(4-methoxybenzyloxy)-1-ethenyl-2-trifluoroacetyl-3,4-dihydro-1H-isoquinoline 
• 1314094-16-0 (-)-(R)-6,8-bis-(4-methoxybenzyloxy)-1-ethenyl-2-trifluoroacetyl-3,4-dihydro-1H-isoquinoline 
• 1314093-81-6 (+)-(S)-6,8-bis(4-methoxybenzyloxy)-3,4-dihydro-1-ethenyl-1H-isoquinoline 
• 1314094-18-2 (-)-(R)-6,8-bis(4-methoxybenzyloxy)-3,4-dihydro-1-ethenyl-1H-isoquinoline 
• 1314093-82-7 C₄₆H₄₄N₂O₇ 
• 1314094-20-6 C₄₆H₄₄N₂O₇ 
• 1314093-91-8 1,3-bis(4-methoxybenzyloxy)-6-(3-hydroxyprop-1-ynyl)-5-[2-(trifluoroacetamido)ethyl]benzene 

Relevant academic research and scientific papers

Formal enantioselective total synthesis of schulzeines A-C via Pd-catalyzed intramolecular asymmetric allylic amination

Formal enantioselective total synthesis of schulzeines A-C was accomplished, featuring highly efficient Pd-catalyzed asymmetric allylic amination using novel diphosphonite ligands (BOPs) to provide 1-vinyltetrahydroisoquinoline key intermediates, as well