85287-65-6

Upstream product

• 66348-32-1 (S)-diethyl malate 2-(1-methyl-1-methoxyethyl ether) 
• 106976-85-6 (E)-(2S,3R)-1-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-5-phenyl-pent-4-ene-2,3-diol 
• 99-33-2 3,5-dinitrobenoyl chloride 
• 66348-33-2 (S)-1,2,4-butanetriol 2-(1-methyl-1-methoxyethyl ether) 
• 32233-43-5 2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol 

Downstream Products

• 85287-64-5 (S)-butane-1,2,4-triol 2,4-acetonide 
• 85287-66-7 3,5-Dinitro-benzoic acid (S)-2,2-dimethyl-[1,3]dioxan-4-ylmethyl ester 
• 105183-53-7 2-[(R)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenoxycarbonyloxy-propyl]-oxazole-4-carboxylic acid methyl ester 
• 105228-50-0 2-[(S)-3-((S)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-2-phenoxycarbonyloxy-propyl]-oxazole-4-carboxylic acid methyl ester 
• 32233-44-6 2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]acetaldehyde 
• 32233-43-5 2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol 

Relevant academic research and scientific papers

Facile access to (S)-1,2,4-butanetriol and its derivatives

The synthesis of (S)-1,2,4-butanetriol from the readily available (S)-malic acid in one step using borane-dimethyl sulfide is described.

ON THE FORMATION OF THE 1,2-ACETONIDE OF (+), (-), AND (+/-) 1,2,4-BUTANETRIOL AND ITS CORRESPONDING ALDEHYDE

The acetonides 1 and 3 are components of a 9:1 equilibrium established during their formation.