In 2019.0 CHEM-EUR J published article about NUCLEOPHILIC-SUBSTITUTION REACTIONS; ARMED GLYCOSYL DONORS; N-PENTENYL GLYCOSIDES; RESTRICTION STRATEGY; OXOCARBENIUM IONS; PROTECTING GROUPS; REACTIVITY; MECHANISMS; ACETALS in [Panza, Matteo; Yasomanee, Jagodige P.; Demchenko, Alexei, V] Univ Missouri, Dept Chem & Biochem, One Univ Blvd, St Louis, MO 63121 USA; [Civera, Monica; Belvisi, Laura] Univ Milan, Dept Chem, I-20133 Milan, Italy in 2019.0, Cited 50.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. Formula: C7H8O
Presented herein is a study of the conformation and reactivity of highly reactive thioglycoside donors. The structural studies have been conducted using NMR spectroscopy and computational methods. The reactivity of these donors has been investigated in bromine-promoted glycosylations of aliphatic and sugar alcohols. Swift reaction times, high yields, and respectable 1,2-cis stereoselectivity were observed in a majority of these glycosylations.
Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Panza, M; Civera, M; Yasomanee, JP; Belvisi, L; Demchenko, AV or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles