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  • COOTE 4-Pi-Photocyclization Revised

    Rights statement: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.orglett.9b03613

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4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential. / Britten, Tom; Kemmitt, Paul D.; Halcovitch, Nathan et al.
In: Organic Letters, Vol. 21, No. 22, 15.11.2019, p. 9232-9235.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Britten, T, Kemmitt, PD, Halcovitch, N & Coote, S 2019, '4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential', Organic Letters, vol. 21, no. 22, pp. 9232-9235. https://doi.org/10.1021/acs.orglett.9b03613

APA

Britten, T., Kemmitt, P. D., Halcovitch, N., & Coote, S. (2019). 4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential. Organic Letters, 21(22), 9232-9235. https://doi.org/10.1021/acs.orglett.9b03613

Vancouver

Britten T, Kemmitt PD, Halcovitch N, Coote S. 4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential. Organic Letters. 2019 Nov 15;21(22):9232-9235. Epub 2019 Nov 7. doi: 10.1021/acs.orglett.9b03613

Author

Britten, Tom ; Kemmitt, Paul D. ; Halcovitch, Nathan et al. / 4‐π-Photocyclization of 1,2-Dihydropyridazines : An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential. In: Organic Letters. 2019 ; Vol. 21, No. 22. pp. 9232-9235.

Bibtex

@article{392de3143d32490a89ec7dcdfce8821b,
title = "4‐π-Photocyclization of 1,2-Dihydropyridazines: An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential",
abstract = "The 4-π-photocyclization of a range of 1,2-dihydropyridazines is described, generating bicyclic 1,2-diazetidines in high yields on multigram scale. The key bicyclic 1,2-diazetidines are versatile synthetic intermediates and were easily converted into a range of novel derivatives, including functionalized 1,2-diazetidines, cyclobutenes, cyclobutanes, and 1,3-dienes.",
author = "Tom Britten and Kemmitt, {Paul D.} and Nathan Halcovitch and Susannah Coote",
note = "This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright {\textcopyright} American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.orglett.9b03613",
year = "2019",
month = nov,
day = "15",
doi = "10.1021/acs.orglett.9b03613",
language = "English",
volume = "21",
pages = "9232--9235",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "22",

}

RIS

TY - JOUR

T1 - 4‐π-Photocyclization of 1,2-Dihydropyridazines

T2 - An Approach to Bicyclic 1,2-Diazetidines with Rich Synthetic Potential

AU - Britten, Tom

AU - Kemmitt, Paul D.

AU - Halcovitch, Nathan

AU - Coote, Susannah

N1 - This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.orglett.9b03613

PY - 2019/11/15

Y1 - 2019/11/15

N2 - The 4-π-photocyclization of a range of 1,2-dihydropyridazines is described, generating bicyclic 1,2-diazetidines in high yields on multigram scale. The key bicyclic 1,2-diazetidines are versatile synthetic intermediates and were easily converted into a range of novel derivatives, including functionalized 1,2-diazetidines, cyclobutenes, cyclobutanes, and 1,3-dienes.

AB - The 4-π-photocyclization of a range of 1,2-dihydropyridazines is described, generating bicyclic 1,2-diazetidines in high yields on multigram scale. The key bicyclic 1,2-diazetidines are versatile synthetic intermediates and were easily converted into a range of novel derivatives, including functionalized 1,2-diazetidines, cyclobutenes, cyclobutanes, and 1,3-dienes.

U2 - 10.1021/acs.orglett.9b03613

DO - 10.1021/acs.orglett.9b03613

M3 - Journal article

VL - 21

SP - 9232

EP - 9235

JO - Organic Letters

JF - Organic Letters

SN - 1523-7060

IS - 22

ER -