243462-70-6

Basic information

• Product Name: 5-O-Benzyl-4a-carba-2,3-O-isopropylidene-β-L-lyxofuranose
• Synonyms: 5-O-Benzyl-4a-carba-2,3-O-isopropylidene-β-L-lyxofuranose
• CAS NO: 243462-70-6
• Molecular Weight: 278.348
• Mol File: 243462-70-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-O-Benzyl-4a-carba-2,3-O-isopropylidene-β-L-lyxofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 5-O-Benzyl-4a-carba-2,3-O-isopropylidene-β-L-lyxofuranose(243462-70-6)
• EPA Substance Registry System: 5-O-Benzyl-4a-carba-2,3-O-isopropylidene-β-L-lyxofuranose(243462-70-6)

Safety Data

• Hazardous Substances Data: 243462-70-6(Hazardous Substances Data)

Upstream product

• 117307-62-7 (3aR,6aR)-6-Benzyloxymethyl-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-one 
• 243462-69-3 (3aR,6S,6aR)-6-Benzyloxymethyl-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-one 
• 89291-76-9 (1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol 

Relevant articles and documents

Chiral pool synthesis of 4a-substituted carbocyclic cyclopentanoid nucleoside precursors, II

Suitable protected 4,4a-anhydro-cyclopentane derivatives have been used for the straight-forward of cyclopentanoid nucleoside precursors. Thus, by simple transformations nucleoside precursors modified at the positions C(4), C(4a) and C(4,4a) as well as side-chain modified derivatives were accessible. The structures of the key intermediates were determined by x-ray analyses.