130353-17-2

Upstream product

• 150-78-7 1,4-dimethoxybezene 
• 109715-12-0 2,3-O-Isopropyliden-2-C-methyl-5-O-p-toluolsulfonyl-D-ribo-pentonsaeure-γ-lacton 
• 130464-15-2 (-)-5-iodo-2,3-O-isopropylidene-2-C-methyl-D-ribolactone 
• 130353-07-0 (-)-(2S,3R)-5-(2,5-dimethoxyphenyl)-3,4-dihydroxy-3,4-O-isopropylidene-4-methylpentene 
• 130353-06-9 Dithiocarbonic acid O-[(2,5-dimethoxy-phenyl)-((4R,5R)-2,2,4-trimethyl-5-vinyl-[1,3]dioxolan-4-yl)-methyl] ester S-methyl ester 
• 130353-05-8 (2S,3R)-1-(2,5-dimethoxyphenyl)-1,2,3-trihydroxy-2,3-O-isopropylidene-2-methylpent-4-ene 
• 130353-11-6 C₁₁H₁₆O₆ 
• 85963-85-5 (-)-(2R,3R)-methyl 2,3-dihydroxy-2,3-O-isopropylidene-2-methylpent-4-enoate 
• 130353-10-5 (+)-(2R,3R)-2,3-dihydroxy-2,3-O-isopropylidene-2-methylpent-4-enoic acid 
• 130353-12-7 (-)-(2S,3R)-2,3-dihydroxy-2,3-O-isoproylidene-2-methylpent-4-enol 

Relevant academic research and scientific papers

Anthracyclinones. 5. Glucosaccharino-1,4-lactone as a Chiral Template for the Synthesis of New Anthracyclinones

Alkylation of dimethoxybenzene 16 with the chiral aldehyde derivative 14 prepared in six steps from α-D-glucosaccharino-1,4-lactone 3 afforded the adduct 17.After suitable transformation of 17, A ring closure was stereoselectively performed using SnCl4 at