University of Sussex
Browse

File(s) not publicly available

A novel cyclisation strategy for the synthesis of lactonamycin: A new route to highly functionalised heterocyclic rings

journal contribution
posted on 2023-06-07, 21:40 authored by Philip J Parsons, Johnathan Board, Alexander J Waters, Peter B Hitchcock, Florian Wakenhut, Daryl S Walter
A novel thermal cascade reaction equivalent to the well-known [2+2+2] cycloaddition has been developed which is clean and reliable and does not involve the use of metal ions. This highly efficient method has been used to construct a model for the synthesis of the antibiotic lactonamycin. The utility of this new sequence for the formation of furans is also reported.

History

Publication status

  • Published

Journal

Synlett

ISSN

09365214

Issue

19

Volume

-

Page range

3243-3246

Department affiliated with

  • Chemistry Publications

Full text available

  • No

Peer reviewed?

  • Yes

Legacy Posted Date

2012-02-06

Usage metrics

    University of Sussex (Publications)

    Categories

    No categories selected

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC