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Search for "SET-promoted photocyclization" in Full Text gives 1 result(s) in Beilstein Journal of Organic Chemistry.

Direct and indirect single electron transfer (SET)-photochemical approaches for the preparation of novel phthalimide and naphthalimide-based lariat-type crown ethers

  • Dae Won Cho,
  • Patrick S. Mariano and
  • Ung Chan Yoon

Beilstein J. Org. Chem. 2014, 10, 514–527, doi:10.3762/bjoc.10.47

Graphical Abstract
  • combined observations made in these investigations demonstrate the unique features of SET-promoted photocyclization reactions that make them well-suited for the use in the synthesis of functionalized crown ethers. In addition, while some limitations exist for the general use of SET-photochemical reactions
  • in large-scale organic synthesis, important characteristics of the photoinduced macrocyclization reactions make them applicable to unique situations in which high temporal and spatial control is required. Keywords: lariat-type crown ethers; SET-promoted photocyclization; α-silylether-terminated
  • efficient fashion. Previous studies [31][32][33][34][62][63][64][65][66][67] in our laboratories resulted in the development, mechanistic elucidation, and synthetic application of various kinds of SET-promoted photocyclization reactions of α-trialkylsilyl donor-linked imide acceptor systems and led to an
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Published 27 Feb 2014
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