Issue 33, 2022

Haber-independent, asymmetric synthesis of the marine alkaloid epi-leptosphaerin from a chitin-derived chiral pool synthon

Abstract

Chitin-derived platforms are emerging as valuable chemical entities for the construction of nitrogenous fine chemicals in processes independent of Haber ammonia. However, much of the work in this area has focused on achiral platforms that limit routine entry into enantiopure, bio-based N-chemical space. Herein, dihydroxyethyl acetamidofuran (Di-HAF), a chiral synthon readily available from chitin, has been transformed into the marine alkaloid epi-leptosphaerin. This work extends the fledgling Haber-independent synthesis concept to enantiopure chemical space not routinely accessible from existing achiral platforms.

Graphical abstract: Haber-independent, asymmetric synthesis of the marine alkaloid epi-leptosphaerin from a chitin-derived chiral pool synthon

Supplementary files

Article information

Article type
Paper
Submitted
12 Jul 2022
Accepted
26 Jul 2022
First published
26 Jul 2022

Org. Biomol. Chem., 2022,20, 6562-6565

Haber-independent, asymmetric synthesis of the marine alkaloid epi-leptosphaerin from a chitin-derived chiral pool synthon

J. C. Neville, M. Y. Lau, T. Söhnel and J. Sperry, Org. Biomol. Chem., 2022, 20, 6562 DOI: 10.1039/D2OB01251K

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