@article{7b9f7a404bf14113b89ff6cf82a5b842,
title = "Red-Light-Induced N, N ′-Dipropyl-1,13-dimethoxyquinacridinium-Catalyzed [3+2] Cycloaddition of Cyclopropylamines with Alkenes or Alkynes",
abstract = "A red-light-mediated [3+2] annulation of cyclopropylamines with akenes or alkynes in the presence of N,N'-dipropyl-1,13-dimethoxyquinacridinium is reported. An array of cyclopentane or cyclopentene derivatives with diverse functional groups have been obtained in moderate to excellent yields under mild conditions.",
keywords = "[3+2] cycloaddition, alkenes, alkynes, cyclopropylamines, dipropyldimethoxyquinacridinium, photoredox catalysis",
author = "Stull, {Savannah M.} and Liangyong Mei and Gianetti, {Thomas L.}",
note = "Funding Information: We are grateful to the University of Arizona and the ACS Petroleum Research Fund (grant no. 59631-DNI3) for financially supporting this work. All NMR data were collected in the NMR facility of the Department of Chemistry and Biochemistry at the University of Arizona, and we thank Dr. Jixun Dai for his help. The purchase of the Bruker NEO 500 MHz spectrometer was supported by the National Science Foundation (Grant No. 1920234) and by the University of Arizona.AmeicanChemical SocieyPeoleumReseachFund(59631-DNI3)Natonal ScienceFoundaion1920234UnivesiytofAizona Publisher Copyright: {\textcopyright} 2021. Thieme. All rights reserved.",
year = "2022",
month = jul,
day = "1",
doi = "https://doi.org/10.1055/a-1665-9220",
language = "English (US)",
volume = "33",
pages = "1194--1198",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "12",
}