107938-43-2

Upstream product

• 81177-24-4 (S,S)-1,4-bis(benzyloxy)-2,3-epoxybutane 
• 195374-95-9 (2S,4R,5S)-4,5-Bis-benzyloxymethyl-2-phenylethynyl-[1,3]dioxolane 
• 210104-38-4 (S)-3-((1R,2S)-3-Benzyloxy-1-benzyloxymethyl-2-hydroxy-propoxy)-5-phenyl-pent-4-ynethioic acid S-tert-butyl ester 
• 210104-32-8 (2R,3S)-1,4-Bis-benzyloxy-3-methoxymethoxy-butan-2-ol 
• 69010-01-1 (2R*,3S*)-1,4-bis(benzyloxy)butane-2,3-diol 
• 107779-33-9 (+/-)-erythro-3-amino-1,4-bis-benzyloxy-butan-2-ol 

Downstream Products

• 107779-33-9 L-erythro-3-amino-1,4-bis-benzyloxy-butan-2-ol 

Relevant academic research and scientific papers

Desymmetrization of meso-1,2-diols via chiral oxazaborolidine-mediated ring-cleavage of acetal derivatives with silyl ketene S,O-acetal

Desymmetrization of meso-1,2-diols leading to enantiomerically enriched MOM and MEM ethers is realized via chiral oxazaborolidine-mediated enantioselective ring-cleavage reaction of the acetal derivatives with silyl ketene S,O-acetal.

Selective Manipulation of Hydroxy Groups in (2S,3S)-Threitol

Systematic transformation of diethyl (2R,3R)-tartrate into a number of protected or functionalized derivatives of threitol, which are important precursors for many natural products, is carried out employing reductive and oxidative cleavage reactions of be