4.8 Article

Construction of Complex Cyclobutane Building Blocks by Photosensitized [2+2] Cycloaddition of Vinyl Boronate Esters

Journal

ORGANIC LETTERS
Volume 23, Issue 9, Pages 3496-3501

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c00938

Keywords

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Funding

  1. NIH [GM127545, 1S10 OD020022-1]
  2. ACS Teva Pharmaceuticals Marc A. Goshko Memorial Grant Program [86428-TEV]
  3. NSF

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This study presents a photosensitized [2 + 2] cycloaddition reaction for the straightforward access to complex cyclobutane scaffolds. Mechanistic studies suggest an activation mode involving energy transfer to the styrenyl alkene rather than the vinyl boronate ester.
Cyclobutyl moieties in drug molecules are rare, and in general, they are minimally substituted and stereochemically simple. Methods to assemble structurally complex cyclobutane building blocks suitable for rapid diversification are thus highly desirable. We report herein a photosensitized [2 + 2] cycloaddition with vinyl boronate esters affording straightforward access to complex, densely functionalized cyclobutane scaffolds. Mechanistic studies suggest an activation mode involving energy transfer to the styrenyl alkene rather than the vinyl boronate ester.

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