88481-66-7

Upstream product

• 88481-65-6 (4S,5S)-5-Allyl-4-hydroxymethyl-2-phenyl-1,3-dioxan 
• 88481-64-5 (2S,3S)-3-(2-propenyl)-1,2,4-butanetriol 
• 73828-22-5 (2S,3R)-3-Allyl-2-Hydroxybernsteinsaeure-diethylester 
• 1339946-61-0 (S)-2-((S)-1,4-dioxaspiro[4.5]decan-2-yl)-pent-4-en-1-ol 
• 1231913-19-1 (S)-2-(1,4-dioxaspiro[4.5]decan-2-yl)-pent-4-enal 
• 88481-62-3 (2S,3R)-3-Allyl-2-(1-methoxy-1-methylethoxy)bernsteinsaeure-diethylester 
• 100-52-7 benzaldehyde 

Downstream Products

• 88481-68-9 (R)-2-((benzyloxy)methyl)pent-4-en-1-ol 

Relevant academic research and scientific papers

A stereodivergent approach to carbahexofuranoses: Synthesis of carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-allofuranose, carba-β-d-idofuranose, carba-α-d- galactofuranose and carba-β-d-talofuranose

A stereodivergent route, starting from d-glyceraldehyde derivative, employing Wittig olefination-Claisen rearrangement protocol is reported for the synthesis of six novel carbahexofuranoses - carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-all

Enantiomerically Pure Building Blocks for Syntheses from Branched Malates

Isocitric acid lactone (13) and the chiral building blocks (2S,3R)-4-bromo-1,2-epoxy-3-methyl-butane (21), cis- and trans 2,3-epoxy-2-methylsuccinates (23, 24), and the singly protected (2R)-2-methyl-, -2-allyl- and -2-benzyl-1,3-propanediols (32a, b, c)