Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kevin Lloyd Greenman"'
Autor:
Edward J. Sullivan, Kevin Lloyd Greenman, J. J. Kim Wright, Xu Yuan, Wei Chen, Subhabrata Sen, James B. Aggen, Li Lianfa, Andrew M. K. Pennell, Derek Hansen, Penglie Zhang, Daniel J. Dairaghi, Trevor T. Charvat
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 23:1228-1231
A novel series of CCR1 antagonists based on the 1-(4-phenylpiperazin-1-yl)-2-(1H-pyrazol-1-yl)ethanone scaffold was identified by screening a compound library utilizing CCR1-expressing human THP-1 cells. SAR studies led to the discovery of the highly
Autor:
Kevin Lloyd Greenman, Aakriti Jain, Adam M. Johns, Kent Kemmish, Anastassia Kanavarioti, Chris R. Melville, Mark Hamalainen, William Andregg
Publikováno v:
ELECTROPHORESIS. 33:3529-3543
With the recent advances in electron microscopy (EM), computation, and nanofabrication, the original idea of reading DNA sequence directly from an image can now be tested. One approach is to develop heavy atom labels that can provide the contrast req
Autor:
David L. Van Vranken, Abu Z M Saleh, Susan B. Billings, John J. Krolewski, Kevin Lloyd Greenman
Publikováno v:
Biochemistry. 44:10822-10827
Elevated levels of IL-6 and IL-11 are associated with multiple myeloma, rheumatoid arthritis, hypercalcemia, cancer cachexia, and Castleman's disease. Madindoline A (MadA), isolated from Streptomyces nitrosporeus K93-0711, specifically inhibits the g
Publikováno v:
Tetrahedron. 61:6438-6441
Palladium can catalyze the insertion of ethyl diazoacetate into benzyl bromides. The key step in the catalytic cycle is the migratory insertion of a carbene, derived from ethyl diazoacetate, into a Pd–C bond.
Publikováno v:
Journal of the American Chemical Society. 125:4518-4526
A strategy to achieve ortho substitution of phenols initiated by an ortho-palladation to create coumarins was examined. Indeed, treatment of alkynoates with electron-rich phenols in the presence of a palladium catalyst and an acid does generate couma
Publikováno v:
Tetrahedron. 57:5219-5225
Palladium(II) salts catalyze the Kirmse reaction of allylsulfides with trimethylsilyldiazomethane (TMSD) to give homoallylsulfides. Similarly, TMSD can intercept ArPdX intermediates generated during Stille couplings to give benzhydryl derivatives. Th
Publikováno v:
ChemInform. 32
Palladium(II) salts catalyze the Kirmse reaction of allylsulfides with trimethylsilyldiazomethane (TMSD) to give homoallylsulfides. Similarly, TMSD can intercept ArPdX intermediates generated during Stille couplings to give benzhydryl derivatives. Th
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[14781-45-4] C10H2CuF12O4 (MW 477.66) InChI = 1S/2C5H2F6O2.Cu/c2*6-4(7,8)2(12)1-3(13)5(9,10)11;/h2*1,12H;/q;;+2/p-2/b2*2-1-; InChIKey = HZXGNBMOOYOYIS-PAMPIZDHSA-L (catalyzes diazo compound decomposition and ylide formation;3 carbene additions4) Alte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2eeb5e880bd486be313028d3456b43c
https://doi.org/10.1002/047084289x.rc227.pub2
https://doi.org/10.1002/047084289x.rc227.pub2
Publikováno v:
ChemInform. 35
The natural product phakellistatin 13 cyclo-(TrpProPheGlyProThrLeu) was synthesized. Photosensitized oxidation of phakellistatin 13 gave the natural products phakellistatin 3 and isophakellistatin 3, demonstrating for the first time that a tryptophan
Publikováno v:
Organic letters. 6(11)
The natural product phakellistatin 13 cyclo-(TrpProPheGlyProThrLeu) was synthesized. Photosensitized oxidation of phakellistatin 13 gave the natural products phakellistatin 3 and isophakellistatin 3, demonstrating for the first time that a tryptophan