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.
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.
Pei-Jun Yang and Zhuo Chai
Org. Biomol. Chem., 2023,21, 465-478
Abstract
Over the past three decades, the catalytic enantioselective desymmetrization of meso-aziridines has evovled to be a ready synthetic toolkit for efficient construction of diverse useful nitrogen-containing molecules bearing contiguous stereocenters.
Seokhwi Park, In-Soo Myeong and Won-Hun Ham
Org. Biomol. Chem., 2024,22, 894-926
Abstract
The flexible synthetic strategy utilizing syn,syn-, syn,anti-, anti,syn-oxazines enabled the synthesis of 30 diverse polyhydroxylated alkaloids.