Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Joseph P. Konopelski"'
Publikováno v:
Organic letters, vol 20, iss 14
Cooper, JK; Li, K; Aubé, J; Coppage, DA; & Konopelski, JP. (2018). Application of the DP4 Probability Method to Flexible Cyclic Peptides with Multiple Independent Stereocenters: The True Structure of Cyclocinamide A. Organic Letters, 20(14), 4314-4317. doi: 10.1021/acs.orglett.8b01756. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/7s54p7c3
Cooper, JK; Li, K; Aubé, J; Coppage, DA; & Konopelski, JP. (2018). Application of the DP4 Probability Method to Flexible Cyclic Peptides with Multiple Independent Stereocenters: The True Structure of Cyclocinamide A. Organic Letters, 20(14), 4314-4317. doi: 10.1021/acs.orglett.8b01756. Lawrence Berkeley National Laboratory: Retrieved from: http://www.escholarship.org/uc/item/7s54p7c3
Copyright © 2018 American Chemical Society. A DP4 protocol has been successfully utilized to establish the true structure of the natural product cyclocinamide A, a flexible cyclic peptide with four isolated stereocenters. Benchmarking the necessary
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https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6faa75af76cd4b09dd76717bd4ef088f
https://escholarship.org/uc/item/7s54p7c3
https://escholarship.org/uc/item/7s54p7c3
Publikováno v:
Tetrahedron. 70:5283-5290
Enantiomerically pure β-lactams bearing a Weinreb amide functionality at the C3 position have been shown to be excellent substrates for α-alkylation reactions, generating C3 quaternary centers with predictable absolute stereochemistry. In addition,
Publikováno v:
Tetrahedron Letters. 54:1482-1485
A new and potentially general synthetic route toward unsymmetrical benzo[b]thienyl-thienylethene compounds is described, with specific focus on conjugation of a ferrocene to the benzo[b]thiophene subunit. The route proceeds in an overall yield of 17%
Publikováno v:
Organic Letters. 14:2054-2057
The cyclocinamides possess a unique β(2)αβ(2)α 14-membered tetrapeptide core. The initially reported biological data and intriguing structure, which was without full stereochemical identification, necessitated synthesis of both nominal (all-S) cy
Autor:
Andrew S. Myers, R. Scott Lokey, Grant A. Hartzog, Nathaniel B. Zuckerman, Walter M. Bray, Tiffani K. Quan, Joseph P. Konopelski
Publikováno v:
ChemMedChem. 7:761-765
Follow my lead! NSC 670224, previously shown to be toxic to Saccharomyces cerevisiae at low micromolar concentrations, potentially acts via a mechanism of action related to that of tamoxifen (NSC 180973), breast cancer drug. The structure of NSC 6702
Autor:
Shaowei Chen, William M. Hewitt, Xiongwu Kang, Xiang Li, Joseph P. Konopelski, Nathaniel B. Zuckerman
Publikováno v:
Analytical Chemistry. 84:2025-2030
Ruthenium nanoparticles were cofunctionalized with pyrene and histidine moieties through Ru═carbene π bonds. The selective complexation of the histidine moiety with transition-metal ions led to a marked diminishment of the emission peak at 490 nm
Autor:
Nathaniel B. Zuckerman, Shaowei Chen, Joseph P. Konopelski, Xiongwu Kang, Wei Chen, Debraj Ghosh
Publikováno v:
The Journal of Physical Chemistry C. 114:18146-18152
Stable ruthenium nanoparticles protected by 1-octynyl fragments were synthesized by a wet chemical method. Transmission electron microscopic measurements showed that the resulting particles exhibited an average core diameter of 2.55 ± 0.15 nm with w
Publikováno v:
The Journal of Physical Chemistry C. 113:16988-16995
Ruthenium nanoparticles functionalized with pyrene moieties were prepared by olefin metathesis reactions of carbene-stabilized nanoparticles with 1-vinylpyrene and 1-allylpyrene (referred to as Ru═VPy and Ru═APy, respectively). 1H NMR spectroscop
Publikováno v:
Journal of Nanoparticle Research. 11:1895-1903
Janus nanoparticles were prepared by taking advantage of interfacial ligand exchange reactions of hydrophobic hexanethiolate-protected gold nanoparticles with hydrophilic 2-(2-mercaptoethoxy)ethanol (MEA). A monolayer of the particles was first forme
Autor:
Lauren E. Brown, Joseph P. Konopelski
Publikováno v:
Organic Preparations and Procedures International. 40:411-445
(2008). TURNING THE CORNER: RECENT ADVANCES IN THE SYNTHESIS OF THE WELWITINDOLINONES. Organic Preparations and Procedures International: Vol. 40, No. 5, pp. 411-445.