1426682-75-8

Upstream product

• 1425495-08-4 C₁₀H₁₄Br₂O₅ 
• 1425495-06-2 C₇H₈O₄ 
• 100-39-0 benzyl bromide 
• 191033-22-4 (R)-5-((1R,2S)-3-Bromo-1,2-dihydroxy-propyl)-5H-furan-2-one 
• 172749-97-2 5,6-di-O-acetyl-7-bromo-2,3,7-trideoxy-D-arabino-hept-2-enono-1,4-lactone 
• 191032-75-4 3,5,6-tri-O-acetyl-2,7-dibromo-2,7-dideoxy-D-glycero-D-ido-heptono-1,4-lactone 
• 116386-12-0 2,7-dibromo-2,7-dideoxy-D-glycero-D-ido-heptono-1,4-lactone 
• 89-67-8 α-D-glucoheptonic γ-lactone 

Downstream Products

• 1425495-11-9 C₁₄H₁₆O₄S 
• 1425495-12-0 C₁₅H₁₈O₆S₂ 
• 1425495-13-1 C₁₄H₁₅N₃O₃S 

Relevant academic research and scientific papers

Deoxythiosugar derivatives with Furano, Pyrano, and septano motifs from L -gulono-1,4-lactone and D-glycero-D-gulo-heptono-1,4-lactone

A short synthesis of thiosugar derivatives mimicking furanose, pyranose, and septanose structures has been achieved starting from L-gulono-1,4-lactone and D-glucoheptono-1,4-lactone. Different strategies used in the synthesis are: (1) a nucleophilic displacement and Michael addition; (2) epoxide ring opening and Michael addition; (3) epoxide ring opening and nucleophilic displacement process; and (4) double nucleophilic displacement. All of these reactions used benzyltriethylammonium tetrathiomolybdate, (BnEt3N) 2MoS4 as the sulfur-transfer reagent. Copyright