512171-75-4

Upstream product

• 512171-73-2 (3R,4S)-1-(p-anisyl)-3-benzyloxy-4-[(Z)-3-(t-butyldiphenylsilyloxy)-1-propenyl]-2-azetidinone 
• 512171-62-9 (3R,4S)-1-(p-anisyl)-3-benzyloxy-4-(3-hydroxy-1-propenyl)-2-azetidinone 
• 512171-61-8 (3R,4S)-1-(p-anisyl)-3-benzyloxy-4-(2-formylvinyl)-2-azetidinone 
• 148968-08-5 (+)-(3R,4R)-1-(p-anisyl)-3-benzyloxy-4-formyl-2-azetidinone 
• 24424-99-5 di-tert-butyl dicarbonate 
• 512171-74-3 (+)-(3R,4S)-3-benzyloxy-4-[(Z)-3-(t-butyldiphenylsilyloxy)-1-propenyl]-2-azetidinone 

Downstream Products

• 512171-78-7 methyl (2Z,6Z)-(4S,5S)-5-(t-butyloxycarbonyl)amino-4-benzyloxy-8-(t-butyldiphenylsilyloxy)-2,6-octadienoate 
• 512171-77-6 (4Z)-(2R,3S)-3-(t-butyloxycarbonyl)amino-2-benzyloxy-6-(t-butyldiphenylsilyloxy)-4-hexenal 
• 512171-80-1 (-)-(5S,6S)-1-allyl-5-benzyloxy-6-[(Z)-(t-butyldiphenylsilyloxy)-1-propenyl]-1,2,5,6-tetrahydro-2-pyridinone 
• 512171-79-8 (+)-(5S,6S)-5-benzyloxy-6-[(Z)-(t-butyldiphenylsilyloxy)-1-propenyl]-1,2,5,6-tetrahydro-2-pyridinone 
• 512171-60-7 (+)-(8S,8aS)-8-(benzyloxy)-3,5,8,8a-tetrahydro-5-indolizidinone 
• 512171-76-5 (+)-(4Z)-(2R,3S)-3-(t-butyloxycarbonyl)amino-2-benzyloxy-6-(t-butyldiphenylsilyloxy)-4-hexen-1-ol 

Relevant academic research and scientific papers

Facile transformation of 2-azetidinones to 2-piperidones: Application to the synthesis of the indolizidine skeleton and (8S,8aS)-perhydro-8-indolizinol

The highly functionalized bicyclic lactam 7 was prepared from diolefinic-2-piperidone 18 by the use of ruthenium-catalyzed RCM, and in turn, 18 was derived via a two-carbon addition process from readily accessible 4-olefinic-2-azetidinone 13. Bicyclic lac