Concise Total Syntheses of Leuconoxine‐Type Alkaloids Enabled by Palladium/Norbornene‐Catalyzed Pyrrole Difunctionalization
Concise total syntheses of five leuconoxine-type alkaloids, i.e., chloromelodinine, leuconodine A, leuconodine F, melodinine E, and leuconoxine, are achieved through a pyrrole-centered strategy. The approach features a newly developed palladium/norbornene-catalyzed pyrrole double C─H functionalization reaction to generate the core skeleton and a divergent oxidative dearomatization to complete the end game. In addition, no protecting group was employed, and the strategic use of a chloro substituent offers a number of advantages in these syntheses, which could have implications beyond this work. The discovery of an unusual chloro 1,2-migration reaction enabled the first total synthesis of chloromelodinine E. This work represents the shortest syntheses of these natural products to date with 10-11 total steps.
Authors
- Guangbin Dong (ORCID: https://orcid.org/0000-0003-1331-6015)
- Renhe Li (ORCID: https://orcid.org/0000-0001-5269-4735)
- Qi Zhu
- Meng Yu (ORCID: https://orcid.org/0000-0003-0234-5902)
- Xin Liu (ORCID: https://orcid.org/0000-0001-8355-4217)
- Yun Zhou (ORCID: https://orcid.org/0000-0003-1945-5876)
Institutions
- University of Illinois Chicago (US)
- University of Chicago (US)
- Physical Sciences (United States) (US)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2025-03-31
- DOI
- https://doi.org/10.1002/anie.202502736
- Citations
- 5
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 4.68
Funders
- National Institute of General Medical Sciences