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- Novel 3-O-α-L-cladinosyl sixteen-membered macrolide antibacterials. Alan K. Mallams, Randall R. Rossman
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 799
- Roxithromycin degradation by acidic hydrolysis and photocatalysis. Anna Kwiecień, Jan Krzek, Paweł Żmudzki, Urszula Matoga, Maciej Długosz, Krzysztof Szczubiałka, Maria Nowakowska
, Anal. Methods
, 2014
, 6
, 6414
- Branched-chain sugars. Part VII. The synthesis of D-mycarose and D-cladinose. B. Flaherty, W. G. Overend, N. R. Williams
, J. Chem. Soc. C
, 1966
, 398
- Modification of post-PKS tailoring steps through combinatorial biosynthesis. Uwe Rix, Carsten Fischer, Lily L. Remsing, Jürgen Rohr
, Nat. Prod. Rep.
, 2002
, 19
, 542
- Type I polyketide biosynthesis in bacteria (Part A—erythromycin biosynthesis). Bernard J. Rawlings
, Nat. Prod. Rep.
, 2001
, 18
, 190
- A comprehensive review of glycosylated bacterial natural products. Sherif I. Elshahawi, Khaled A. Shaaban, Madan K. Kharel, Jon S. Thorson
, Chem. Soc. Rev.
, 2015
, 44
, 7591
- A conformational exploration of the protonated and unprotonated macrolide antibiotic roxithromycin: comparative study by molecular dynamics and NMR spectroscopy in solution. Josyane Gharbi-Benarous, Patrick Ladam, Marcel Delaforge, Jean-Pierre Girault
, J. Chem. Soc., Perkin Trans. 2
, 1992
, 1989
- Post-PKS tailoring steps in natural product-producing actinomycetes from the perspective of combinatorial biosynthesis. Carlos Olano, Carmen Méndez, José A. Salas
, Nat. Prod. Rep.
, 2010
, 27
, 571
- An investigation of the predominant structure of antibiotic azithromycin in chloroform solution through NMR and thermodynamic analysis. Isabel S. Hernandes, Haroldo C. Da Silva, Hélio F. Dos Santos, Eloah P. Ávila, Mauro V. De Almeida, Matheus G. R. Gomes, Diego F. S. Paschoal, Wagner B. De Almeida
, Phys. Chem. Chem. Phys.
, 2022
, 24
, 22845
- A comparative investigation of the consistent valence and extensible systematic force fields. A case study on the conformation of erythromycin A in benzene. José C. Martins, Rudolph Willem, Monique Biesemans
, J. Chem. Soc., Perkin Trans. 2
, 1999
, 1513