| Literature DB >> 30747539 |
Yan Zhang1, Haiqian Zhu1, Yuting Huang1, Qi Hu1, Yu He1, Yihang Wen1, Gangguo Zhu1.
Abstract
A practical one-pot isoindolinone synthesis enabled by RhIII catalysis was developed. The advantage of this protocol is that it does not require pre-preparation of amide substrates, because RhIII participates in two reactions independently. This mild, operationally multicomponent process transforms a wide variety of commercially available aldehydes into the corresponding γ-lactams in good yields, thereby demonstrating that N-pyridin-2-yl benzamide is an effective directing group. Notably, the anxiolytic drugs pagoclone and pazinaclone can be directly prepared by this methodology.Entities:
Year: 2019 PMID: 30747539 DOI: 10.1021/acs.orglett.8b04026
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005