A photochemical C=C cleavage process: toward access to backbone N-formyl peptides

dc.citation.firstpage2932en_US
dc.citation.journalTitleBeilstein Journal of Organic Chemistryen_US
dc.citation.lastpage2938en_US
dc.citation.volumeNumber17en_US
dc.contributor.authorWang, Haopeien_US
dc.contributor.authorBall, Zachary T.en_US
dc.date.accessioned2022-01-21T16:23:57Zen_US
dc.date.available2022-01-21T16:23:57Zen_US
dc.date.issued2021en_US
dc.description.abstractPhoto-responsive modifications and photo-uncaging concepts are useful for spatiotemporal control of peptides structure and function. While side chain photo-responsive modifications are relatively common, access to photo-responsive modifications of backbone N–H bonds is quite limited. This letter describes a new photocleavage pathway, affording N-formyl amides from vinylogous nitroaryl precursors under physiologically relevant conditions via a formal oxidative C=C cleavage. The N-formyl amide products have unique properties and reactivity, but are difficult or impossible to access by traditional synthetic approaches.en_US
dc.identifier.citationWang, Haopei and Ball, Zachary T.. "A photochemical C=C cleavage process: toward access to backbone N-formyl peptides." <i>Beilstein Journal of Organic Chemistry,</i> 17, (2021) Beilstein-Institut: 2932-2938. https://doi.org/10.3762/bjoc.17.202.en_US
dc.identifier.digital1860-5397-17-202en_US
dc.identifier.doihttps://doi.org/10.3762/bjoc.17.202en_US
dc.identifier.urihttps://hdl.handle.net/1911/111928en_US
dc.language.isoengen_US
dc.publisherBeilstein-Instituten_US
dc.rightsThis is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.en_US
dc.rights.urihttps://www.beilstein-journals.org/bjoc/termsen_US
dc.titleA photochemical C=C cleavage process: toward access to backbone N-formyl peptidesen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpublisher versionen_US
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