Category: 114861-22-2

Total synthesis of the alkaloid (-)-codonopsinine from L-xylose was written by Chandrasekhar, S.;Jagadeshwar, V.;Prakash, S. Jaya. And the article was included in Tetrahedron Letters in 2005.Computed Properties of C8H14O5 This article mentions the following:

The enantiopure total synthesis of (-)-codonopsinine (I) is described from com. available L-xylose in 20% overall yield. The key steps included Julia trans olefination and cascade epoxidation-cyclization strategies. In the experiment, the researchers used many compounds, for example, (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2Computed Properties of C8H14O5).

(3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2) belongs to tetrahydrofuran derivatives. Tetrahydrofuran (THF), or oxolane, is mainly used as a precursor to polymers. Being polar and having a wide liquid range, THF is a versatile solvent. Tetrahydrofuran reaction with hydrogen sulfide: In the presence of a solid acid catalyst, tetrahydrofuran reacts with hydrogen sulfide to give tetrahydrothiophene.Computed Properties of C8H14O5

Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Synthesis of 5-fluoro-4-deoxy-β-L-uridine was written by Dong, Chun-Hong;Qi, Xiu-Xiang;Yu, Xue-Jun;Chang, Jun-Biao. And the article was included in Gaodeng Xuexiao Huaxue Xuebao in 2004.Category: tetrahydrofurans This article mentions the following:

The title compound was prepared in 10 steps starting from L-xylose via condensation of 1-O-acetyl-2,3,5-tri-O-benzoyl-β-L-ribofuranose with silylated 5-fluorouracil. The structures of compounds were identified by the MS, UV, IR, ¹H NMR spectra and elemental analyses. In the experiment, the researchers used many compounds, for example, (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2Category: tetrahydrofurans).

(3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2) belongs to tetrahydrofuran derivatives. Tetrahydrofuran (THF) is a Lewis base that bonds to a variety of Lewis acids such as I2, phenols, triethylaluminum and bis(hexafluoroacetylacetonato)copper(II). Tetrahydrofuran reaction with hydrogen sulfide: In the presence of a solid acid catalyst, tetrahydrofuran reacts with hydrogen sulfide to give tetrahydrothiophene.Category: tetrahydrofurans

Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Synthesis of L-3′-hydroxymethylribonucleosides was written by Cooperwood, John S.;Boyd, Vincent;Gumina, Giuseppe;Chu, Chung K.. And the article was included in Nucleosides, Nucleotides & Nucleic Acids in 2000.Name: (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol This article mentions the following:

The target compounds, e.g. I, were synthesized via the key intermediate carbohydrate II, which was synthesized by first selectively protecting the 1′- and 2′-hydroxyl groups followed by selective tosylation of the 5′-hydroxyl group, Dess-Martin oxidation, Wittig olefination, and regioselective hydroboration. The synthesized compounds were evaluated for anti-HIV-1 and anti-HBV activity in human peripheral blood mononuclear cells and 2.2.15 cells; no significant antiviral activity was detected up to 100 μM and 10 μM, resp. In the experiment, the researchers used many compounds, for example, (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2Name: (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol).

(3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2) belongs to tetrahydrofuran derivatives.Tetrahydrofuran has many industry uses as a solvent including in natural and synthetic resins, high polymers, fat oils, rubber, polymer. THF (Tetrahydrofuran) is also used as a starting material for the synthesis of poly(tetramethylene ether) glycol (PTMG), etc.Name: (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol

Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem

Carbohydrate-based approach to four enantiomerically pure 2-naphthylmethyl 3-hydroxy-2-methylbutanoates was written by Doboszewski, Bogdan;Herdewijn, Piet. And the article was included in Tetrahedron Letters in 2008.Application of 114861-22-2 This article mentions the following:

Chiral pool approach using D-glucose, L-xylose, and D– and L-arabinoses was used to obtain four stereoisomeric 3-hydroxy-2-methylbutanoic acids with well defined configurations. The acids were isolated as fluorescent 2-naphthylmethyl esters after reaction with 2-naphthyldiazomethane. In the experiment, the researchers used many compounds, for example, (3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2Application of 114861-22-2).

(3aS,5S,6R,6aS)-5-(Hydroxymethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 114861-22-2) belongs to tetrahydrofuran derivatives. Solid acid catalysis, and the advantages often associated with their use, have been proved equally efficient for the synthesis of tetrahydrofurans or furans. Tetrahydrofuran reaction with hydrogen sulfide: In the presence of a solid acid catalyst, tetrahydrofuran reacts with hydrogen sulfide to give tetrahydrothiophene.Application of 114861-22-2

Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem