The glycosidic C—C bond's construction is used by the majority of techniques. These C-glycosylation techniques are grouped here according to the glycosyl donor precursors that are often utilised in the synthesis of O-glycosides and are simple for non-experts to obtain. The glycosyl halides, glycals, sugar acetates, lactones, lactones, lactones, 1,2-anhydro sugars, thioglycosides/sulfoxides/sulfones, selenoglycosides/telluroglycosides, methyl glycosides, and glycosyl imidates/phosphates are some of these substances. Glycosyl electrophilic/cationic species, anionic species, radical species, or transition-metal complexes can all play a role in C-glycosylation processes in terms of their underlying mechanisms, which are covered as subcategories under each kind of sugar precursor. The Claisen, Ramberg-Bäcklund, and 1,2-Wittig rearrangements, which frequently include coordinated pathways, are only a few examples of intramolecular rearrangements. These rearrangements also fall under the category of C-glycosylations. The development of pyranoside/furanoside rings following the creation of the C-glycosylations provides an alternative to the C-glycosylations.
Stanislaw Dzwigaj
Sorbonne University, France
Thomas J Webster
Interstellar Therapeutics, United States
Dai Yeun Jeong
Asia Climate Change Education Center, Korea, Republic of
Vladislav Sadykov
Boreskov Institute of Catalysis, Russian Federation
Beatrice Vincenti
Sapienza University of Rome, Italy
Haibo Ge
Texas Tech University, United States
Pengju Wu
School of Energy and Power Engineering Jiangsu University, China
Yaxin Su
Donghua University, China
Isabel Oller Alberola
Plataforma Solar de Almería, Spain
Majed Alamoudi
King Abdulaziz University, Saudi ArabiaSubmit your abstract Today
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