Vogel, James A. et al. published their research in Organic Letters in 2022 | CAS: 582-52-5

(3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 582-52-5) belongs to tetrahydrofuran derivatives. Tetrahydrofuran and dihydrofuran form the basic structural unit of many naturally occurring scaffolds like gambieric acid A and ciguatoxin, goniocin, and some biologically active molecules. Tetrahydrofuran can also be produced, or synthesised, via catalytic hydrogenation of furan. This process involves converting certain sugars into THF by digesting to furfural. An alternative to this method is the catalytic hydrogenation of furan with a nickel catalyst.Recommanded Product: 582-52-5

Synthesis of Highly Reactive Sulfone Iminium Fluorides and Their Use in Deoxyfluorination and Sulfur Fluoride Exchange Chemistry was written by Vogel, James A.;Hammami, Rania;Ko, Ara;Datta, Hiya;Eiben, Yael N.;Labenne, Karley J.;McCarver, Ellis C.;Yilmaz, Ebrar Z.;Melvin, Patrick R.. And the article was included in Organic Letters in 2022.Recommanded Product: 582-52-5 This article mentions the following:

The synthesis of sulfone iminium fluorides (SIFs) RS(O)(F)=N+(CH3)R1OTf– (R = Ph, Me, 4-fluorophenyl; R1 = n-Pr, cyclopropyl, 4-fluorophenyl, etc.), a reactive class of sulfur(VI) mols. was reported. The synthesis is tolerant of a variety of substituents on the sulfur and nitrogen components. The SIF reagents were applied to the deoxyfluorination of alcs. such as 1-(tert-butyl) 2-Me (2S,4S)-4-hydroxypyrrolidine-1,2-dicarboxylate and carboxylic acids R2CO2H (R2 = 4-bromophenyl, butan-2-yl, adamant-1-yl, etc.), providing high yields of fluorinated products in 60 s at room temperature The SIF reagents were then utilized in sulfur fluoride exchange (SuFEx), creating the first ionic SuFEx products C6H5S(O)(OR3)=N+(CH3)(Bn)OTf– (R3 = Ph, 6-methylpyridin-2-yl, 2-oxo-2H-chromen-7-yl, etc.) to date. In the experiment, the researchers used many compounds, for example, (3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 582-52-5Recommanded Product: 582-52-5).

(3aR,5S,6S,6aR)-5-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-ol (cas: 582-52-5) belongs to tetrahydrofuran derivatives. Tetrahydrofuran and dihydrofuran form the basic structural unit of many naturally occurring scaffolds like gambieric acid A and ciguatoxin, goniocin, and some biologically active molecules. Tetrahydrofuran can also be produced, or synthesised, via catalytic hydrogenation of furan. This process involves converting certain sugars into THF by digesting to furfural. An alternative to this method is the catalytic hydrogenation of furan with a nickel catalyst.Recommanded Product: 582-52-5

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