Tailored amination enables switchable synthesis of α- and γ-amino acid derivatives from extended quinone methides
Abstract Unnatural α- and γ-amino acids display a diverse range of biological activities and serve as crucial intermediates in pharmaceutical production. Specifically, the synthesis of such molecules has been highly sought after in both academia and industry. Nevertheless, their direct synthesis fro...
Saved in:
| Main Authors: | Chao-Gang Zhang, Yu-Ping Tang, Qingqin Huang, Yong-Ke Qiu, Hailong Yan, Lei Dai |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-07-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-60749-7 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Development of a novel family of antifungal agents based on a quinone methide oxime framework
by: Monika Janeczko, et al.
Published: (2025-04-01) -
Synthesis and Trapping of the Elusive <i>Ortho</i>-Iminoquinone Methide Derived from α-Tocopheramine and Comparison to the Case of α-Tocopherol
by: Anjan Patel, et al.
Published: (2025-08-01) -
Amino Acids and Biogenic Amines Evolution during the Estufagem of Fortified Wines
by: Vanda Pereira, et al.
Published: (2015-01-01) -
Amines tuned controllable carbonylation for the synthesis of γ-lactones and 1,4-diones
by: Yuanrui Wang, et al.
Published: (2025-07-01) -
Trophic activity of pedofauna in two gardens of Saint-Petersburg (experience of using the express bait-lamina test methid)
by: A. A. Kuzmina, et al.
Published: (2024-11-01)