Zobrazeno 1 - 10
of 136
pro vyhledávání: '"D. Reichl"'
Autor:
Sara Fallah, Dustin Duncan, Kyle D. Reichl, Michael J. Smith, Wenyu Wang, John A. Porco, Lauren E. Brown, Luke Whitesell, Nicole Robbins, Leah E. Cowen
Publikováno v:
Microbiology Spectrum, Vol 12, Iss 4 (2024)
ABSTRACTCandida albicans, one of the most prevalent human fungal pathogens, causes diverse diseases extending from superficial infections to deadly systemic mycoses. Currently, only three major classes of antifungal drugs are available to treat syste
Externí odkaz:
https://doaj.org/article/0310e0d547f54976a2f68da74ed7b338
Publikováno v:
Suchttherapie.
Autor:
Kyle D. Reichl, John A. Porco, Michael J. Smith, Thomas J. Heavey, David F. Coker, Scott E. Schaus, Randolph A. Escobar
Publikováno v:
Journal of the American Chemical Society. 141:148-153
Asymmetric synthesis of the biologically active xanthone dimer griffipavixanthone is reported along with its absolute stereochemistry determination. Synthesis of the natural product is accomplished via dimerization of a p-quinone methide using a chir
Publikováno v:
Journal of the American Chemical Society. 140:5969-5975
The first synthesis of the chromanone lactone dimer gonytolide A has been achieved employing vanadium(V)-mediated oxidative coupling of the monomer gonytolide C. An ortho-bromine blocking group strategy was employed to favor para-para coupling and to
Autor:
Alexander T. Radosevich, Emmanuel Hatzakis, Sean M. McCarthy, Kyle D. Reichl, Yi-Chun Lin, Hemant P. Yennawar, Ting Yi Lai
Publikováno v:
Journal of the American Chemical Society. 139:6008-6016
Studies of the stoichiometric and catalytic reactivity of a geometrically constrained phosphorous triamide 1 with pinacolborane (HBpin) are reported. The addition of HBpin to phosphorous triamide 1 results in cleavage of the B-H bond of pinacolborane
Publikováno v:
Journal of the American Chemical Society. 137:5292-5295
We report that a regioselective reductive transposition of primary allylic bromides is catalyzed by a biphilic organophosphorus (phosphetane) catalyst. Spectroscopic evidence supports the formation of a pentacoordinate (σ(5)-P) hydridophosphorane as
Publikováno v:
Journal of the American Chemical Society. 139(40)
We report the concise, biomimetic total synthesis of the dimeric, Diels–Alder natural product griffipavixanthone from a readily accessible prenylated xanthone monomer. The key step utilizes a novel intermolecular [4+2] cycloaddition–cyclization c
Autor:
Matthew D. Reichl, Erich J. Mueller
Publikováno v:
Physical Review A. 93
Motivated by experiments in Munich (M. Schreiber et. al. Science \textbf{349}, 842), we study the dynamics of interacting fermions initially prepared in charge density wave states in one-dimensional bichromatic optical lattices. The experiment sees a
Autor:
William G. Dougherty, Chip Nataro, Chelsea L. Mandell, Owen D. Henn, Kyle D. Reichl, W. Scott Kassel
Publikováno v:
Journal of Organometallic Chemistry. 696:3882-3894
The electrochemistry of 1,1′-bis(diphenylphosphino)cobaltocenium hexafluorophosphate ([dppc][PF6]), 1,1′-bis(dicyclohexylphosphino)cobaltocenium hexafluorophosphate ([dcpc][PF6]), 1,1′-bis(di-iso-propylphosphino)cobaltocenium hexafluorophosphat
Publikováno v:
ChemInform. 46
The reductive transposition of primary allylic halides is catalyzed by a biphilic organophosphorus catalyst.