Recent Advancements in Glycosylation Reactions: An Access to Privileged C- and S-glycosides

RP Pandey, B Tiwari, AK Pandey… - Current Organic …, 2025 - benthamdirect.com
Glycosylation reactions are central to carbohydrate chemistry due to their broad applications
in drug development and biological probes. Despite presenting significant challenges and …

Reactivity Switch in Glycal Dienes toward Different Nucleophiles: Mechanistic Insight and Applications toward the Synthesis of Naphthalene-Fused Pyran Derivatives

RP Pandey, B Tiwari, N Sharma, K Giri… - The Journal of Organic …, 2024 - ACS Publications
The stereo-and regioselective formation of chiral molecules is an interesting and important
topic in organic synthesis due to its wide applicability and intricacy during synthesis. Herein …

Pd-catalyzed stereoselective synthesis of chromone C-glycosides

MK Sharma, B Tiwari, N Hussain - Chemical Communications, 2024 - pubs.rsc.org
Herein, we present an efficient Pd-catalysed method for stereoselective synthesis of
chromone C-glycosides from various glycals. We successfully applied this method to various …

Synthesis of Branched Sugars and Chiral Aromatic Building Blocks Derived from Glycals

M Maheswari, N Hussain - Synlett, 2025 - thieme-connect.com
The transformation of sugar enolic ethers into branched sugars through CH activation or
cross-coupling reaction represents a compelling strategy in carbohydrate chemistry. These …

Glycals as Chiral Synthons in Organic Synthesis of Privileged Molecular Scaffolds

R Sagar, Y Sagar - Chemistry–An Asian Journal - Wiley Online Library
Chirality is a vital characteristic of molecules and crucial for biological functioning. Glycals
are unsaturated chiral sugars that contain an enolic double bond within the ring structure …

Five-membered ring systems: With more than 1 N atom

L Yet - Progress in Heterocyclic Chemistry, 2024 - Elsevier
The synthesis and chemistry of pyrazoles, imidazoles, 1, 2, 3-triazoles, 1, 2, 4-triazoles, and
tetrazoles were actively pursued in 2023. No attempt was made to incorporate all the …