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Modular, Scalable Total Synthesis of Lapparbin with a Noncanonical Biaryl Linkage.
- Source :
-
Angewandte Chemie International Edition . 10/14/2024, Vol. 63 Issue 42, p1-9. 9p. - Publication Year :
- 2024
-
Abstract
- We report the development of a novel synthetic approach for the highly strained atrop‐Tyr C‐6‐to‐Trp N‐1′ linkage, which can be executed on a decagram scale using a modular strategy involving palladium‐catalyzed C−H arylation followed by Larock macrocyclization. The first total synthesis of lapparbin (1) was achieved by applying this synthetic strategy. Furthermore, the modular synthesis utilizing C−H arylation and Larock macrocyclization, discovered in the total synthesis of lapparbin (1), was demonstrated to be applicable to various arbitrary biaryl linkages, including non‐natural types. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CYCLIC peptides
*PALLADIUM
*CATALYSIS
*ARYLATION
Subjects
Details
- Language :
- English
- ISSN :
- 14337851
- Volume :
- 63
- Issue :
- 42
- Database :
- Academic Search Index
- Journal :
- Angewandte Chemie International Edition
- Publication Type :
- Academic Journal
- Accession number :
- 180150636
- Full Text :
- https://doi.org/10.1002/anie.202409987