Intramolecular photochemical [2 + 1]-cycloadditions of nucleophilic siloxy carbenes†
Version 3 2024-06-19, 09:36Version 3 2024-06-19, 09:36
Version 2 2024-06-06, 10:48Version 2 2024-06-06, 10:48
Version 1 2022-03-14, 08:12Version 1 2022-03-14, 08:12
journal contribution
posted on 2024-06-19, 09:36 authored by A Bunyamin, C Hua, A Polyzos, DL PriebbenowVisible light induced singlet nucleophilic carbenes undergo rapid [2 + 1]-cycloaddition with tethered olefins to afford unique bicyclo[3.1.0]hexane and bicyclo[4.1.0]heptane scaffolds.
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Journal
Chemical ScienceVolume
13Pagination
3273-3280Location
Cambridge, Eng.Publisher DOI
Open access
- Yes
Link to full text
ISSN
2041-6520eISSN
2041-6539Language
EnglishPublication classification
C1 Refereed article in a scholarly journalIssue
11Publisher
Royal Society of ChemistryUsage metrics
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No categories selectedKeywords
ACYLSILANESALKENESCATALYZED ENANTIOSELECTIVE CYCLOPROPANATIONC-CChemistryChemistry, MultidisciplinaryDONOR-ACCEPTOR CYCLOPROPANESFUNCTIONALIZATIONMETAL-FREEPhysical SciencesScience & TechnologySILYLACYLATIONSSTEREOSELECTIVITYTRANSFORMATIONS3404 Medicinal and biomolecular chemistry3405 Organic chemistry
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