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- Sampling rifamycin conformational variety by cruising through crystal forms: implications for polymorph screening and for biological models. Alessia Bacchi, Mauro Carcelli, Giancarlo Pelizzi
, New J. Chem.
, 2008
, 32
, 1725
- Stereoselective synthesis of the C-21 to C-27 segment of rifamycin-S. A. V. Rama Rao, J. S. Yadav, V. Vidyasagar
, J. Chem. Soc., Chem. Commun.
, 1985
, 55
- The derivation of carbon–proton internuclear distances in organic natural products from 13C relaxation rates and nuclear overhauser effects. Neri Niccolai, Claudio Rossi, Paolo Mascagni, William A. Gibbons, Vittorio Brizzi
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 239
- Modelling vinyl ether formation in rifamycin S. John A. Murphy, Christopher W. Patterson, Nicholas F. Wooster
, J. Chem. Soc., Chem. Commun.
, 1988
, 294
- Siderophore conjugation with cleavable linkers boosts the potency of RNA polymerase inhibitors against multidrug-resistant E. coli. Carsten Peukert, Anna C. Vetter, Hazel L. S. Fuchs, Kirsten Harmrolfs, Bianka Karge, Marc Stadler, Mark Brönstrup
, Chem. Sci.
, 2023
, 14
, 5490
- Modifications, biological origin and antibacterial activity of naphthalenoid ansamycins. Natalia Skrzypczak, Piotr Przybylski
, Nat. Prod. Rep.
, 2022
, 39
, 1653
- Biomolecular dynamics and electron spin resonance spectra of copper complexes of antitumour agents in solution. Part 2.—Rifamycins. Riccardo Basosi, Rebecca Pogni, Enzo Tiezzi, William E. Antholine, Lynn C. Moscinsky
, J. Chem. Soc., Faraday Trans. 1
, 1987
, 83
, 3675
- Polyketide construction via hydrohydroxyalkylation and related alcohol C–H functionalizations: reinventing the chemistry of carbonyl addition. Anne-Marie R. Dechert-Schmitt, Daniel C. Schmitt, Xin Gao, Takahiko Itoh, Michael J. Krische
, Nat. Prod. Rep.
, 2014
, 31
, 504
- The identification and assay of mixtures of antibiotics by electrophoresis in agar gel. J. W. Lightbown, P. de Rossi
, Analyst
, 1965
, 90
, 89
- Semi-synthetic zwitterionic rifamycins: a promising class of antibiotics; survey of their chemistry and biological activities. Krzysztof Bujnowski, Ludwik Synoradzki, Radosław C. Darłak, Thomas A. Zevaco, Eckhard Dinjus
, RSC Adv.
, 2016
, 6
, 114758