Xu Yan, Wei Feng, Jiong Xu Ng, Jiaxin Li, Ying Liu, Bo Zhang, Pan-Lin Shao and Yu Zhao
Chem. Soc. Rev., 2025,54, 7966-8018
Abstract
This review aims to provide a thorough overview of recent advancements in the synthesis of chiral vicinal amino alcohols, with a particular focus on strategic developments over the past two decades.
Yuchen Yang, Jia-Long Wu, Sheng-Ye Zhang, Xu Liu, Teng Sun, Yanan Zhao and Lijia Wang
Chem. Sci., 2026,17, 2356-2363
Abstract
Fluorinated counteranions enable enantioselective synthesis of vicinal amino alcohols.
Guoqi Huang, Yu Wu, Hegui Gong and Yunrong Chen
Org. Biomol. Chem., 2023,21, 6111-6114
Abstract
An economical route providing quick access to chiral vicinal amino alcohols bearing a symmetric β-sec-alkyl group was developed.
Yuntao Yuan, Wenhao Wang, Yong Wang, Daming Feng, Shiyong Peng, Chunhua Ge and Peng Huang
Org. Biomol. Chem., 2026,24, 3435-3441
Abstract
A highly efficient iodine-catalyzed Z-to-E isomerization of enamides has been developed, featuring mild reaction conditions, excellent yields, broad substrate scope, and gram-scale synthesis.
Padmanava Barik, Subhasmita Sahoo, Usharani Das and Santosh Kumar Nanda
Chem. Commun., 2025,61, 11581-11596
Abstract
The photocatalytic and electrocatalytic cross aza–pinacol coupling has been a potential method for the rapid access to amino alcohols in an eco-friendly manner.