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Synthesis of the Proposed Structure of Celacarfurine and Analogues Using Sequential Cascade Ring Expansion Reactions

Title: Synthesis of the Proposed Structure of Celacarfurine and Analogues Using Sequential Cascade Ring Expansion Reactions
Authors: Tam JKF; Waddell LJN; Palate KY; Whitwood AC; Longcake A; Probert MR; Grogan G; Lichman BR; Unsworth WP
Source: Organic Letters, 30 January 2026
Publisher Information: American Chemical Society
Publication Year: 2026
Collection: Newcastle University Library ePrints Service
Description: The first synthesis of the proposed structure of spermidine derived macrocyclic alkaloid celacarfurine is described. A versatile synthetic strategy has been developed based on sequential cascade ring expansion reactions, with high dilution conditions not needed for any of the steps. The same general strategy was also used to generate a series of macrocyclic analogues. The physical properties and spectroscopic data obtained for our synthetic product do not match those reported for the isolated alkaloid.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/310467; https://eprints.ncl.ac.uk/fulltext.aspx?url=310467/54CB60AF-1C46-4D54-B91F-0C52395C0D4B.pdf&pub_id=310467
Availability: https://eprints.ncl.ac.uk/310467
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.60718E89
Database: BASE