Yuchen Yang, Jia-Long Wu, Sheng-Ye Zhang, Xu Liu, Teng Sun, Yanan Zhao and Lijia Wang
Chem. Sci., 2026, Advance Article
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.