1100106-37-3

Basic information

• Product Name: (1R,3S,4S,5S,8R)-4-benzyloxy-8-hydroxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane
• Synonyms: (1R,3S,4S,5S,8R)-4-benzyloxy-8-hydroxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane
• CAS NO: 1100106-37-3
• Molecular Weight: 266.294
• Mol File: 1100106-37-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,3S,4S,5S,8R)-4-benzyloxy-8-hydroxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,3S,4S,5S,8R)-4-benzyloxy-8-hydroxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane(1100106-37-3)
• EPA Substance Registry System: (1R,3S,4S,5S,8R)-4-benzyloxy-8-hydroxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane(1100106-37-3)

Safety Data

• Hazardous Substances Data: 1100106-37-3(Hazardous Substances Data)

Upstream product

• 1100106-38-4 C₁₄H₁₆O₅ 

Downstream Products

• 1100106-43-1 C₁₉H₂₆O₆ 

Relevant articles and documents

Stereodivergent synthesis of new amino sugars, furanodictines A and B, starting from d-glucuronolactone

An efficient and divergent strategy for the total synthesis of the first 3,6-dihydroaminosugars, furanodictines A (2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-d-glucofuranose) and B (2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-d-mannofuranose), has been developed. The synthetic process is featured by readily accessible and stereodefined manipulation of highly functionalized bicyclic tetrahydrofuran derivatives incorporating the glucuronolactone (common starting material)-derived skeleton.