A low temperature, vinylboronate ester-mediated, iterative cross-coupling approach to xanthomonadin polyenyl pigment analogues

Madden, Katrina S., Knowles, Jonathan and Whiting, Andrew (2019) A low temperature, vinylboronate ester-mediated, iterative cross-coupling approach to xanthomonadin polyenyl pigment analogues. Tetrahedron, 75 (45). p. 130657. ISSN 0040-4020

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Madden et al - A low temperature, vinylboronate ester-mediated, iterative cross-coupling approach to xanthomonadin polyenyl pigment analogues AAM.pdf - Accepted Version
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Official URL: https://doi.org/10.1016/j.tet.2019.130657

Abstract

Approaches to the polyene natural product xanthomonadin, an octaenyl electron-deficient bacterial photoprotective agent, and its debromo analogue, were developed. These involved the iterative cross-coupling of multiple C2-fragments, using a vinylboronate ester as a formal vinyl dianion equivalent. Vinyl iodide starting materials undergo Heck-Mizoroki cross-coupling at ambient temperatures, allowing further iododeboronation to derive the next vinyl iodide. This works in a highly effective manner to access systems of up to pentaene chain length. However, final assembly of polyenylboronates with such polyenyl iodides through their Suzuki-Miyaura cross-coupling was less successful, even at lower temperatures, reflecting the extreme sensitivity of such octaenylxanthomonadin analogues. Despite this, the mild cross-coupling conditions could be effectively applied to the assembly of a range of useful polyenyl building blocks, as well as a truncated pentaenyl-debromoxanthomonadin analogue.

Item Type: Article
Uncontrolled Keywords: Polyene, Iterative cross-coupling, Vinylboronate, Heck-Mizoroki reaction, Suzuki-Miyaura cross-coupling, iodo-deboronation
Subjects: F100 Chemistry
Department: Faculties > Health and Life Sciences > Applied Sciences
Depositing User: Paul Burns
Date Deposited: 10 Oct 2019 12:43
Last Modified: 11 Oct 2020 08:01
URI: http://nrl.northumbria.ac.uk/id/eprint/41071

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