162435-01-0

Upstream product

• 162434-98-2 1,4-di-O-benzyl-L-threitol 2,3-cyclic ethyl orthoformate 
• 162434-99-3 (2R,3R)-1,4-bis(benzyloxy)-3-vinyl-2-butanol mesylate 
• 123125-14-4 1,4-di-O-benzyl-2-chloro-2-deoxy-3-O-formyl-L-erythritol 
• 113368-83-5 (2R,3R)-2-(phenylmethoxy)-3-[(phenylmethoxy)methyl]-4-penten-2-ol 
• 81177-24-4 (S,S)-1,4-bis(benzyloxy)-2,3-epoxybutane 
• 162435-00-9 (2S,3R)-3-azido-1,4-bis(benzyloxy)-2-vinylbutane 

Downstream Products

• 159721-93-4 (2'S,3'S)-1-<2',3'-bis(benzyloxymethyl)azetidinyl>thymine 
• 159721-90-1 (2'S,3'S)-1-<2',3'-bis(benzyloxymethyl)azetidinyl>uracil 
• 159721-86-5 (2S,3S)-N¹-nitroso-2,3-bis(benzyloxymethyl)azetidine 
• 159721-87-6 (2S,3S)-N¹-amino-2,3-bis(benzyloxymethyl)azetidine 
• 159721-85-4 (2S,3S)-2,3-bis(benzyloxymethyl)azetidine 
• 162435-02-1 (2S,3R)-3-azido-1,4-bis(benzyloxy)-2-hydroxymethylbutane mesylate 

Relevant academic research and scientific papers

Enantiospecific synthesis of [(2'S, 3'S)-bis(hydroxymethyl)azetidin-1-yl]pyrimidine nucleosides as potential antiviral agents

The enantiospecific synthesis of [(2'S, 3'S)-bis(hydroxymethyl)azatidin-1-yl]pyrimidine nucleotides 22, 25, and 27 was achieved via construction of the base on the 1-aminoacetidine 18 prepared from (+)-diethyl-L-tartrate, and they are the first members of