Search Results - "Rathman, Benjamin M."

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  1. 1

    Late-Stage Sidechain-to-Backbone Macrocyclization of N‑Amino Peptides by Rathman, Benjamin M, Del Valle, Juan R

    Published in Organic letters (25-02-2022)
    “…Cysteine-containing N-amino peptides undergo chemoselective reactions with haloaldehydes to afford ethylene-bridged cyclic peptides. This bis-alkylation…”
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    Journal Article
  2. 2

    Synthesis and biological evaluation of backbone-aminated analogues of gramicidin S by Rathman, Benjamin M., Allen, Jessie L., Shaw, Lindsey N., Del Valle, Juan R.

    Published in Bioorganic & medicinal chemistry letters (01-08-2020)
    “…[Display omitted] We report the parallel synthesis of gramicidin S derivatives featuring backbone N-amino substituents. Analogues were prepared by…”
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    Journal Article
  3. 3

    Design and Synthesis of Biologically Relevant N-Aminated Macrocyclic Peptidomimetics by Rathman, Benjamin M

    Published 01-01-2023
    “…Protein-protein interactions play important roles at all levels of cellular organization and thus are therapeutically relevant targets for the treatment of a…”
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    Dissertation
  4. 4

    Fluoro-curcuminoids and curcuminoid-BF2 adducts: Synthesis, X-ray structures, bioassay, and computational/docking study by Laali, Kenneth K., Rathman, Benjamin M., Bunge, Scott D., Qi, Xin, Borosky, Gabriela L.

    Published in Journal of fluorine chemistry (01-11-2016)
    “…[Display omitted] •Synthesis of α-fluorinated curcuminoids by direct mono- and difluorination.•Synthesis of ring fluorinated curcuminoids.•Isolation and…”
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    Journal Article
  5. 5

    Mild conversion of propargylic alcohols to α,β-unsaturated enones in ionic liquids (ILs); a new ‘metal free’ life for the Rupe rearrangement by Nandi, Ganesh C., Rathman, Benjamin M., Laali, Kenneth K.

    Published in Tetrahedron letters (13-11-2013)
    “…A mild and selective transition metal free protocol for the conversion of propargylic alcohols to cyclic and acyclic α,β-unsaturated enones via the Rupe…”
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    Journal Article
  6. 6

    Fluoro-curcuminoids and curcuminoid-BF^sub 2^ adducts: Synthesis, X-ray structures, bioassay, and computational/docking study by Laali, Kenneth K, Rathman, Benjamin M, Bunge, Scott D, Qi, Xin, Borosky, Gabriela L

    Published in Journal of fluorine chemistry (01-11-2016)
    “…A series of α-carbonyl fluorinated curcuminoids were synthesized by direct mono- and difluorination with Selectfluor (F-TEDA-BF4) at r.t. without using a base…”
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    Journal Article