Search Results - "Rathman, Benjamin M."
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Late-Stage Sidechain-to-Backbone Macrocyclization of N‑Amino Peptides
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
Synthesis and biological evaluation of backbone-aminated analogues of gramicidin S
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
Design and Synthesis of Biologically Relevant N-Aminated Macrocyclic Peptidomimetics
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
Fluoro-curcuminoids and curcuminoid-BF2 adducts: Synthesis, X-ray structures, bioassay, and computational/docking study
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
Mild conversion of propargylic alcohols to α,β-unsaturated enones in ionic liquids (ILs); a new ‘metal free’ life for the Rupe rearrangement
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
Fluoro-curcuminoids and curcuminoid-BF^sub 2^ adducts: Synthesis, X-ray structures, bioassay, and computational/docking study
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