Demonstrates efficient synthesis of glycosyl sulfonamides, suggesting a novel approach in organic chemistry.
We developed an efficient methodology for synthesizing C ‐acyl‐glycosyl sulfonamides via a carbonylative coupling reaction, using 1‐iodo‐glycals as substrates. A wide range of aromatic, heteroaromatic, and aliphatic sulfonamides was explored, employing Mo(CO) 6 as a safe, solid source of carbon monoxide gas. This approach enabled the preparation of novel glycosyl sulfonamides featuring a C ‐acyl‐linked framework under mild reaction conditions, achieving good to excellent yields.
No takes yet. Share an insight, caveat, or question.
Silva et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: