Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nicole M. Hewlett"'
Autor:
Qiang Yang, Lawrence C. Creemer, Peter L. Johnson, James A. Knobelsdorf, Benjamin M. Nugent, Carl V. De Amicis, Sarah Ryan, Elizabeth O. McCusker, Gregory T. Whiteker, Nakyen Choy, Beth A. Lorsbach, Nicole M. Hewlett, Fangzheng Li, Belgin Canturk, Nicholas R. Babij, Michelle Smith
Publikováno v:
Organic Process Research & Development. 20:661-667
The 1H and 13C NMR chemical shifts of 48 industrially preferred solvents in six commonly used deuterated NMR solvents (CDCl3, acetone-d6, DMSO-d6, acetonitrile-d3, methanol-d4, and D2O) are reported. This work supplements the compilation of NMR data
Publikováno v:
Angewandte Chemie International Edition. 54:2830-2833
The proteasome represents an invaluable target for the treatment of cancer and autoimmune disorders. The application of proteasome inhibitors, however, remains limited to blood cancers because their reactive headgroups and peptidic scaffolds convey u
Autor:
Jetze J. Tepe, Shun Su, Ken S. Feldman, Amanda P. Skoumbourdis, Matthew D. Fodor, Ian B. Seiple, Theresa A. Lansdell, Nicole M. Hewlett, Phil S. Baran
Publikováno v:
Journal of Natural Products. 75:980-985
We report herein that the oroidin-derived alkaloids palau'amine (1), dibromophakellin (2), and dibromophakellstatin (3) inhibit the proteolytic activity of the human 20S proteasome as well as the (i)20S immunoproteasome catalytic core. Palau'amine is
Autor:
Jetze J. Tepe, Nicole M. Hewlett
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[1199-01-5] C9H7NO2 (MW 161.16) InChI = 1S/C9H7NO2/c11-8-6-10-9(12-8)7-4-2-1-3-5-7/h1-5H,6H2 InChIKey = QKCKCXFWENOGER-UHFFFAOYSA-N (reagent used as a masked glycine equivalent and for the formation of heterocyclic structures) Alternate Name: 2-pheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fbb9ce1b95ca2ef8f6c139c281e35eb
https://doi.org/10.1002/047084289x.rn01743
https://doi.org/10.1002/047084289x.rn01743
Autor:
Nicole M. Hewlett, Jetze J. Tepe
(±)-Dibromophakellin has been synthesized in two steps from a known alkene intermediate. The key step in the synthesis is the NBS olefin activation to facilitate the addition of a guanidine molecule across the double bond.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91b36075ccc695da939203afee581558
https://europepmc.org/articles/PMC3162990/
https://europepmc.org/articles/PMC3162990/
Publikováno v:
ChemInform. 41
Autor:
Nicole M. Hewlett, Jetze J. Tepe
Publikováno v:
Organic Letters; Sep2011, Vol. 13 Issue 17, p4550-4553, 4p
Autor:
Choudhary, Dimple1 (AUTHOR), Garg, Sonali1 (AUTHOR), Kaur, Manvinder1 (AUTHOR), Sohal, Harvinder Singh1 (AUTHOR) drharvinder.cu@gmail.com, Malhi, Dharambeer Singh1 (AUTHOR), Kaur, Loveleen1 (AUTHOR), Verma, Meenakshi1 (AUTHOR), Sharma, Ajay1 (AUTHOR), Mutreja, Vishal1 (AUTHOR)
Publikováno v:
Polycyclic Aromatic Compounds. 2023, Vol. 43 Issue 5, p4512-4578. 67p.
Publikováno v:
Angewandte Chemie. Feb2015, Vol. 127 Issue 9, p2872-2875. 4p.