796869-98-2

Upstream product

• 796869-82-4 benzyl (2S,5R)-2-benzyloxycarbonylamino-5-triisopropylsilyloxymethyl-5,6-dihydroxyhexanoate 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 

Downstream Products

• 796869-89-1 benzyl (2S,5S)-5-benzyloxycarbamoyl-2-benzyloxycarbonylamino-5,6-dihydroxyhexanoate 
• 956007-31-1 (3S,3'S)-1-benzyloxy-3-(3'-benzyloxycarbonyl-3'-benzyloxycarbonylaminopropyl)-3-hydroxy-2-azetidinone 
• 796869-92-6 (3S,3'S)-1-benzyloxy-3-(3'-benzyloxycarbonylamino-3'-carboxypropyl)-3-tert-butyldimethylsilyloxy-2-azetidinone 
• 796869-99-3 benzyl (2S,5S)-5-benzyloxycarbamoyl-2-benzyloxycarbonylamino-5-hydroxy-6-methylsulfonyloxyhexanoate 
• 796869-91-5 (3S,3'S)-1-benzyloxy-3-(3'-benzyloxycarbonyl-3'-benzyloxycarbonylaminopropyl)-3-tert-butyldimethylsilyloxy-2-azetidinone 
• 796869-90-4 benzyl (2S,5S)-5-benzyloxycarbamoyl-2-benzyloxycarbonylamino-5-tert-butyldimethylsilyloxy-6-methylsulfonyloxyhexanoate 

Relevant academic research and scientific papers

Synthesis of (-)-tabtoxinine-β-lactam, the phytotoxin of tobacco wildfire disease

Synthesis of (-)-tabtoxinine-β-lactam and its (3R)-isomer, the cause of tobacco wildfire disease, was achieved from L-serine using a zinc-mediated coupling reaction, Sharpless asymmetric dihydroxylation and lactamization of β-mesyloxy benzylhydroxamate amide as the key steps. Georg Thieme Verlag Stuttgart.

Facile synthesis of (-)-tabtoxinine-β-lactam and its (3′R)-isomer

A concise and high yielding synthesis of (-)-tabtoxinine-β-lactam 1, the cause of tobacco wildfire disease, was achieved from l-serine. A concise and high yielding synthesis of (-)-tabtoxinine-β-lactam 1, the cause of tobacco wildfire disease, was achieve