1333388-38-7

Upstream product

• 1316832-00-4 (5R,6S)-5-(benzyloxy)-6-(3-hydroxypropyl)piperidin-2-one 
• 1316831-98-7 (5R,6S)-1-allyl-5-(benzyloxy)-6-(3-hydroxypropyl)piperidin-2-one 
• 1254985-48-2 (R)-1-allyl-3-benzyloxy-2,6-piperidinedione 

Downstream Products

• 1333388-39-8 (3S,8R,8aS)-8-(benzyloxy)-3-[(S)-4-methyl-5-oxo-2,5-dihydrofuran-2-yl]hexahydroindolizin-5(1H)-one 
• 1333388-40-1 (8R,8aS)-8-(benzyloxy)-3-[4-methyl-5-oxo-2,5-dihydrofuran-2-yl]hexahydroindolizin-5(1H)-one 
• 1333388-41-2 (3S,8R,8aS)-8-(benzyloxy)-3-[(2S,4S)-4-methyl-5-oxotetrahydrofuran-2-yl]hexahydroindolizin-5(1H)-one 
• 1333388-37-6 (8R,8aS)-8-(benzyloxy)-5-oxo-octahydroindolizin-3-yl acetate 

Relevant academic research and scientific papers

Concise asymmetric total synthesis of 9-epi-sessilifoliamide J

A 10-step asymmetric synthesis of 9-epi-sessilifoliamide J (20), together with sessilifoliamide J (6), has been accomplished from the key chiral building block 11 via a threo-selective vinylogous Mannich reaction and a Ley oxidation-SmI2-mediated coupling