437609-55-7

Upstream product

• 244023-85-6 (S)-3-(tert-butoxycarbonylamino)-1,5-dioxaspiro[3.2]hexane 
• 1192356-68-5 C₁₆H₂₅NO₅ 
• 77-76-9 2,2-dimethoxy-propane 
• 437609-52-4 (4S,1'S)-4-(2'-tert-butyldimethylsilanyloxy-1'-hydroxyethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 437609-40-0 (S)-4-(acetoxyacetyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 437609-43-3 (4S,1'S)-4-(1',2'-dihydroxyethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 437609-39-7 (S)-1-acetoxy-3-(tert-butoxycarbonylamino)-4-hydroxybutan-2-one 
• 213338-89-7 (S)-3-(tert-butoxycarbonylamino)-2-methyleneoxetane 
• 100-39-0 benzyl bromide 
• 437609-53-5 (4S,1'S)-4-(1'-benzyloxy-2'-tert-butyldimethylsilanyloxyethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 115822-55-4 (4S,1'S)-4-(1'-benzyloxy-2'-oxoethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Stereoselective synthesis of 2-epi-jaspine B via base-catalyzed intramolecular oxy-Michael conjugate addition approach

2-epi-Jaspine B has been synthesized starting from (-)-diethyl tartrate in 12 simple steps and 26.6% overall yield. The key intermediate was obtained via stereoselective base-catalyzed intramolecular oxy-Michael conjugate addition followed by tandem hydro

Synthesis of D-erythro-dihydrosphingosine and D-xylo-phytosphingosine from a serine-derived 1,5-dioxaspiro[3.2]hexane template

Matrix presented A serine-derived 1,5-dioxaspiro[3.2]hexane template is shown to be a useful precursor for both aminodiol and aminotriol sphingoid bases by its conversion to D-erythro-dihydrosphingosine and D-xylo-phytoshingosine.