146467-10-9

Upstream product

• 146467-09-6 (2R,3R-O-isopropylidene)-4S-(N-benzylamino)-5R,6-dihydroxyhexyl-triphenylmethyl ether 
• 146467-07-4 1-benzyl-3S-hydroxy-4R-[1'R,2'R-O-isopropylidene-3'-hydroxy]propyl-azetidin-2-one 
• 146467-06-3 1-benzyl-3S-benzyloxy-4R-[1'R,2'R-O-isopropylidene-3'-hydroxy]propyl-azetidin-2-one 
• 146467-05-2 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3-oxo]propyl-azetidin-2-one 
• 146467-04-1 1-benzyl-3S-benzyloxy-4R-[1'R,2'S-O-isopropylidene-3'R,4'-dihydroxy]butyl azetidin-2-one 
• 146467-03-0 cis-1-benzyl-3S-benzyloxy-4R-[1'R,2'S,3'R,4'-di-O-isopropylidene]butyl-azetidin-2-one 
• 146467-08-5 1-benzyl-3S-hydroxy-4R-[1'R,2'R-O-isopropylidene-3'-triphenylmethoxy]propyl-azetidin-2-one 
• 76-83-5 trityl chloride 

Downstream Products

• 146467-12-1 (R)-tert-Butoxycarbonylamino-((4R,5R)-2,2-dimethyl-5-trityloxymethyl-[1,3]dioxolan-4-yl)-acetic acid 
• 146467-11-0 [(1S,2S)-1-((4R,5R)-2,2-Dimethyl-5-trityloxymethyl-[1,3]dioxolan-4-yl)-2,3-dihydroxy-propyl]-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

Polyhydroxy amino acid derivatives via β-lactams using enantiospecific approaches and microwave techniques

Enantiospecific synthesis has been developed for α-hydroxy β-lactams of predictable absolute configuration starting with readily available carbohydrates. Stereospecific approaches and microwave assisted chemical reactions have been utilized for the prepar

Versatile β-Lactam Synthons: Enantiospecific Synthesis of (-)-Polyoxamic Acid

An optically pure cis-α-hydroxy β-lactam of predictable absolute configuration prepared from readily available D-mannitol has been utilized for the synthesis of the non-natural enantiomer of polyoxamic acid through a series of stereospecific reactions.