79241-07-9

Basic information

• Product Name: (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan
• Synonyms: (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan
• CAS NO: 79241-07-9
• Molecular Weight: 276.332
• Mol File: 79241-07-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan(79241-07-9)
• EPA Substance Registry System: (R)-4-((2S,3R)-3-(benzyloxy)-2,3-dihydrofuran-2-yl)-2,2-dimethyl-1,3-dioxolan(79241-07-9)

Safety Data

• Hazardous Substances Data: 79241-07-9(Hazardous Substances Data)

Upstream product

• 1017236-05-3 (2R,3R,4R,5R)-1,2-O-isopropylidene-3,6-anhydro-4-O-benzyl-5-O-methanesulfonyl-D-glucitol 
• 1167439-17-9 C₁₆H₂₁IO₄ 
• 17087-84-2 (3aS,4R,6R,6aS)-4-chloro-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole 
• 530-26-7 D-Mannose 
• 68144-11-6 1,4-anhydro-2-deoxy-5,6-O-isopropylidene-D-arabinohex-1-enitol 
• 100-39-0 benzyl bromide 
• 7757-38-2 2,3,5,6-di-O-isopropylidene-D-mannofuranose 
• 7757-38-2 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 6160-67-4 (3aS,4R,6R,6aS)-4-chloro-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxole 
• 68144-11-6 1,4-anhydro-2-deoxy-5,6-O-isopropylidene-D-arabino-hex-1-enitol 
• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 

Downstream Products

• 112289-64-2 1-O-acetyl-3-O-benzyl-2-deoxy-2-fluoro-5,6-O-isopropylidne-α-D-glucofuranose 
• 149774-40-3 1-[(2R,3R,4S,5R)-4-Benzyloxy-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-3-phenylselanyl-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 1272376-60-9 1,4-anhydro-3-O-benzyl-2-deoxy-1,2-C-(dichloromethylene)-5,6-O-isopropylidene-D-glycero-D-glucohexitol 

Relevant articles and documents

Synthesis of Bioactive Side-Chain Analogues of TAN-2483B

The fungal metabolite TAN-2483B has a 2,6-trans-relationship across the pyran ring of its furo[3,4-b]pyran-5-one core, which has thwarted previous attempts at its synthesis. We have now developed a chiral pool approach to this core and prepared side-chain

Norrisolide: Total synthesis and related studies

A stereoselective synthesis of (+)-norrisolide is presented. This natural product belongs to a family of marine spongiane diterpenes the structure of which is characterized by a fused γ-lactone-γ-lactol ring system attached to a bicyclic hydrophobic core.

Synthetic studies on norrisolide: Enantioselective synthesis of the norrisane side chain

Norrisolide (1) belongs to a family of marine diterpenes that are characterized by the assembly of a bicyclic core with a unique and highly oxygenated side chain (norrisane side chain). As a prelude to the synthesis of 1, we present herein a short, effici