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
Dai Yeun Jeong
Asia Climate Change Education Center, Korea, Republic of
Enrico Paris
CREA-IT & DIAEE, Italy
Hanna Kierzkowska Pawlak
Lodz University of Technology, Poland
Ling Yin
Cornell University, United States
Tsitsishvili Vladimer
Petre Melikishvili Institute of Physical and Organic Chemistry at the Tbilisi State University, Georgia
Rafia Ahmad
King Abdullah University of Science and Technology, Saudi Arabia
Eun Han Lee
Korea Institute of Energy Research, Korea, Republic of
Neul Ha
Sungkyunkwan University, Korea, Republic of
Shailza Sharma
RMIT University, AustraliaSubmit your abstract Today
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