Four-Component Radical 1, 2-Selenosulfonylation of Allenes
XR Shu, MH Li, C Wu, XN Luo, DQ Yang… - Organic …, 2024 - ACS Publications
Selenosulfones, as pivotal pharmaceutical molecule frameworks, have become a research
hotspot in modern organic synthesis due to their vital need for efficient preparation. Herein …
hotspot in modern organic synthesis due to their vital need for efficient preparation. Herein …
A Radical Activation Strategy for Versatile and Stereoselective N‐Glycosylation
W Ding, X Chen, Z Sun, J Luo, S Wang… - Angewandte Chemie …, 2024 - Wiley Online Library
Previous N‐glycosylation approaches have predominately involved acidic conditions, facing
challenges of low stereoselectivity and limited scope. Herein, we introduce a radical …
challenges of low stereoselectivity and limited scope. Herein, we introduce a radical …
Ring Opening of Aziridines by Pendant Sulfamates Allows for Regioselective and Stereospecific Preparation of Vicinal Diamines
The ring opening of aziridines by pendant sulfamates is a viable strategy for the rapid
preparation of vicinal diamines. Our reaction is compatible with both disubstituted cis-and …
preparation of vicinal diamines. Our reaction is compatible with both disubstituted cis-and …
Incorporating azaheterocycle functionality in intramolecular aerobic, copper-catalyzed aminooxygenation of alkenes
EM DeCicco, N Tlapale-Lara, SM Paradine - RSC advances, 2024 - pubs.rsc.org
Despite the maturity of alkene 1, 2-difunctionalization reactions involving C–N bond
formation, a key limitation across aminofunctionalization methods is incompatibility with …
formation, a key limitation across aminofunctionalization methods is incompatibility with …
Ring-Opening of Aziridines by Pendant Sulfamates Allows for Regioselective and Stereospecific Preparations of Vicinal Diamines
S Sathyamoorthi, S Nagamalla, AA Thomas, A Nirpal… - 2023 - chemrxiv.org
The ring-opening of aziridines by pendant sulfamates is a viable strategy for the rapid
preparation of vicinal diamines. Our reaction is compatible with both di-substituted cis and …
preparation of vicinal diamines. Our reaction is compatible with both di-substituted cis and …