Shamim Fanai-Danesh, Daniel F. Moseley, Kevin M. Foote, Kieran D. Jones, Stephen P. Argent and Hon Wai Lam
Org. Biomol. Chem., 2025,23, 10502-10507
Abstract
The nucleophilic allylation of N-sulfinylamines with allylboron reagents is reported. Bulky N-sulfinylamines react with allyl pinacolboronate using indium catalysis, while others react with potassium allyltrifluoroborate using (thio)urea catalysis.
Hang T. Dang, Arka Porey, Sachchida Nand, Ramon Trevino, Patrick Manning-Lorino, William B. Hughes, Seth O. Fremin, William T. Thompson, Shree Krishna Dhakal, Hadi D. Arman and Oleg V. Larionov
Chem. Sci., 2023,14, 13384-13391
From themed collection:
2023 Chemical Science Covers
Abstract
Sulfinamides can now be readily accessed from carboxylic acids and amines in a direct decarboxylative reaction enabled by the kinetically-driven reactivity of sulfinylamines and acridine photocatalysis.
Miloš Jabczun, Vladimír Nosek and Jiří Míšek
Org. Biomol. Chem., 2023,21, 2950-2954
Abstract
We describe a straightforward one-pot reductive protocol for the synthesis of sulfinamides from sulfonyl chlorides.
Xinyu Zhu, Junliang Wu, Junliang Zhang and Junfeng Yang
RSC Adv., 2025,15, 4532-4535
Abstract
Sulfinamides play a crucial role in organic synthesis and pharmaceuticals.
Yongxin Zhang, Helian Li, Xiaoxiao Yang, Pan Zhou and Chao Shu
Chem. Commun., 2023,59, 6272-6285
From themed collection:
2023 Emerging Investigators
Abstract
This feature article discusses the state-of-play of cyclic sulfinic acid derivative (sultines and cyclic sulfinamides) formation.