Expanding Heteroaromatic and 2-Aminosugar Chemical Space Accessible from the Biopolymer Chitin

Author:

Rossa Thaís A.1,Neville Jessica C.1,Jun Seongmin Paul1,Söhnel Tilo1ORCID,Sperry Jonathan1

Affiliation:

1. Centre for Green Chemical Science, University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand

Abstract

Herein, we report the expansion of chemical space available from chitin, accessible via the biogenic N-platforms 3A5AF, M4A2C, and di-HAF. The biologically active heteroaromatics furo[3,2-d]pyrimidin-4-one and furo[3,2-d]pyrimidin-4-amine can be selectively accessed from 3A5AF and M4A2C, respectively. The chiral pool synthon di-HAF is a viable substrate for Achmatowicz rearrangement, providing streamlined access to 2-aminosugars possessing a versatile hydroxymethyl group at C5.

Funder

University of Auckland

Publisher

MDPI AG

Subject

Organic Chemistry,Inorganic Chemistry,Electrochemistry,Chemistry (miscellaneous)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Sustainable synthesis of nitrogen-rich aromatics from chitin: Opportunities and challenges;Current Opinion in Green and Sustainable Chemistry;2024-10

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