121328-65-2

Upstream product

• 1075748-99-0 4,6-di-O-benzoyl-1,5-anhydro-2-deoxy-D-erythro-hex-1-en-3-ulose 
• 98-88-4 benzoyl chloride 
• 58871-05-9 6-O-Benzoyl-D-glucal 

Downstream Products

• 121328-66-3 C₄₇H₄₅IO₁₀ 
• 121328-67-4 C₅₉H₆₄I₂O₁₆ 
• 121328-72-1 C₆₅H₈₂I₂O₁₄Si₂ 
• 121328-70-9 (2R,3S,4R)-4-((2S,3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-iodo-tetrahydro-pyran-2-yloxy)-3-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-3,4-dihydro-2H-pyran 
• 121328-69-6 (2R,3S,4R)-4-((2S,3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-3-iodo-tetrahydro-pyran-2-yloxy)-2-hydroxymethyl-3,4-dihydro-2H-pyran-3-ol 

Relevant academic research and scientific papers

Efficient synthesis of rare sugar D-allal via reversal of diastereoselection in the reduction of protected 1,5-anhydrohex-1-en-3-uloses: Protecting group dependence of the stereoselection

(Chemical Equation Presented) D-Allal was selectively obtained by reducing bulky-silyl-protected 1,5-anhydrohex-1-en-3-uloses using the NaBH4 - CeCl3·7H2O system. The crucial point of this synthesis is the nature of the pr

On the Controlled Oxidative Coupling of Glycals: A New Strategy for the Rapid Assembly of Oligosaccharides

Controlled oxidative coupling of various glucal triethers with glucals containing a single hydroxy group (either at C4 or C3) and acyloxy groups at the other two positions has been demonstrated.The process is readily reiterated.A concise route to α-linked