874117-65-4

Upstream product

• 874117-64-3 (2S,3R)-3-Trityloxymethyl-oxirane-2-carboxylic acid methyl ester 
• 76-83-5 trityl chloride 
• 142096-78-4 (E)-1-hydroxy-4-(triphenylmethoxy)-2-butene 

Downstream Products

• 874117-56-3 (2S,3S)-2-[1,3]Dithian-2-yl-4-trityloxy-butane-1,3-diol 
• 874117-67-6 (4S,5S)-2,2-Di-tert-butyl-4-trityloxymethyl-[1,3,2]dioxasilinane-5-carbaldehyde 
• 874117-57-4 ((4S,5S)-2,2-Di-tert-butyl-4-trityloxymethyl-[1,3,2]dioxasilinan-5-yl)-methanol 
• 874117-69-8 (4S,5S)-5-Azidomethyl-2,2-di-tert-butyl-4-trityloxymethyl-[1,3,2]dioxasilinane 
• 874117-68-7 Methanesulfonic acid (4S,5R)-2,2-di-tert-butyl-4-trityloxymethyl-[1,3,2]dioxasilinan-5-ylmethyl ester 
• 874117-66-5 (4S,5S)-2,2-Di-tert-butyl-5-[1,3]dithian-2-yl-4-trityloxymethyl-[1,3,2]dioxasilinane 

Relevant academic research and scientific papers

A mild and metal-free synthesis of chiral 2,3-dihydro-3-hydroxymethyl-1,4-benzoxazines

Various functionalized enantiomerically pure 3-hydroxymethyl-1,4-benzoxazine derivatives, including four stereoisomers, were synthesized from chiral 2,3-epoxy-4-trityloxybutanol. The synthesis was mild and metal-free. Yields of 52%–94%, and stereoselectiv

Synthesis of a versatile (S)-3-(hydroxymethyl)butane-1,2,4-triol building block and its application for the stereoselective synthesis of N-homoceramides

(Chemical Equation Presented) A versatile (S)-3-(hydroxymethyl)butane-1,2, 4-triol building block has been synthesized starting from D-isoascorbic acid, a common food preservative. The key transformation in this approach was the introduction of branching