Stereoselective synthesis of medium lactams enabled by metal-free hydroalkoxylation/stereospecific [1,3]-rearrangement
Stereospecific [1,3]-rearrangements are rarely reported method to efficiently build complex organic architectures. Here, the authors describe a metal-free intramolecular hydroalkoxylation/[1,3]-rearrangement sequence affording medium-sized lactams with wide scope, also in an asymmetric fashion.
Main Authors: | Bo Zhou, Ying-Qi Zhang, Kairui Zhang, Ming-Yang Yang, Yang-Bo Chen, You Li, Qian Peng, Shou-Fei Zhu, Qi-Lin Zhou, Long-Wu Ye |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2019-07-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-019-11245-2 |
Similar Items
-
Synthesis of Polysubstituted Tetrahydropyrans by Stereoselective Hydroalkoxylation of Silyl Alkenols: En Route to Tetrahydropyranyl Marine Analogues
by: Carlos Díez-Poza, et al.
Published: (2018-11-01) -
Recent advances in reagent-controlled stereoselective/stereospecific glycosylation
by: Yao, Hui, et al.
Published: (2020) -
Stereoselective oxygenation of bicyclic lactams
by: Cottrell, I, et al.
Published: (2004) -
Towards Dual-Metal Catalyzed Hydroalkoxylation of Alkynes
by: Oscar F. González-Belman, et al.
Published: (2021-06-01) -
Stereospecific total synthesis of beta-lactam antibiotics from peptide precursors.
by: Christie, Michael Allen.
Published: (2024)