138723-41-8

Upstream product

• 13096-62-3 (3R,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-one 
• 138723-27-0 C₁₉H₂₁LiOSi 
• 138723-39-4 (2R,4aR,6S,7R,8R,8aS)-6-(4-Hydroxy-3,3-dimethyl-butyl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 138723-38-3 [2,2-Dimethyl-4-((2S,3S,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-but-3-ynyloxy]-methyl-diphenyl-silane 
• 138723-28-1 (2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-[3,3-dimethyl-4-(methyl-diphenyl-silanyloxy)-but-1-ynyl]-tetrahydro-pyran-2-ol 
• 138723-31-6 (4S,5aR,8R,9aR,9bS)-4-[4-(tert-Butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyl]-3a-methyl-8-phenyl-hexahydro-[1,3]dioxolo[4',5':4,5]pyrano[3,2-d][1,3]dioxine-2-thione 
• 138723-40-7 (2R,4aR,6S,8S,8aS)-6-[4-(tert-Butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyl]-7-methyl-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 138723-30-5 (2R,4aR,6S,8S,8aS)-6-[4-(tert-Butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyl]-8-hydroxy-2-phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-7-one 
• 138723-29-2 (2R,4aR,6S,7R,8R,8aS)-6-[4-(tert-Butyl-dimethyl-silanyloxy)-3,3-dimethyl-butyl]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine-7,8-diol 
• 138723-32-7 tert-Butyl-[2,2-dimethyl-4-((2R,4aR,6S,8aS)-7-methyl-2-phenyl-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-butoxy]-dimethyl-silane 
• 138723-33-8 2,2-Dimethyl-4-((2R,4aR,6S,8aS)-7-methyl-2-phenyl-4,4a,6,8a-tetrahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-butyraldehyde 
• 138723-42-9 (2S,3R,4R,5S,6R)-2-(4-Hydroxy-3,3-dimethyl-butyl)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 

Relevant academic research and scientific papers

Pyranose α-Enones Provide Ready Access to Functionalized trans-Decalins via Bis-Annulated Pyranosides Obtained by Intramolecular Diels-Alder Reactions. A Key Intermediate for Forskolin

Intramolecular Diels-Alder routes for the preparation of bis-annulated pyranosides, as chiral precursors of functionalized trans-decalin rings of terpenoid natural products, have been investigated.