A platform for the discovery of new macrolide antibiotics

Development of a platform for the discovery and practical synthesis of new tetracycline antibiotics

(2016) Fan Liu et al.   CURRENT OPINION IN CHEMICAL BIOLOGY

Synthesis of D -Desosamine and Analogs by Rapid Assembly of 3-Amino Sugars

(2015) Ziyang Zhang et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Structural insights into species-specific features of the ribosome from the pathogenStaphylococcus aureus

(2015) Zohar Eyal et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Total Synthesis of Desmethyl Macrolide Antibiotics

(2015) Rodrigo Andrade   SYNLETT

An Efficient Directed Claisen Reaction Allows for Rapid Construction of 5,6-Disubstituted 1,3-Dioxin-4-ones

(2015) Andrew Myers et al.   SYNTHESIS-STUTTGART

Stereocontrolled Synthesis ofsyn-β-Hydroxy-α-Amino Acids by Direct Aldolization of Pseudoephenamine Glycinamide

(2014) Ian B. Seiple et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

The Evolving Role of Chemical Synthesis in Antibacterial Drug Discovery

(2014) Peter M. Wright et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Binding and Action of CEM-101, a New Fluoroketolide Antibiotic That Inhibits Protein Synthesis

(2010) B. Llano-Sotelo et al.   ANTIMICROBIAL AGENTS AND CHEMOTHERAPY

Revisiting the structures of several antibiotics bound to the bacterial ribosome

(2010) D. Bulkley et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Total Synthesis of Azithromycin

(2009) Hyoung Cheul Kim et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Genetic engineering of macrolide biosynthesis: past advances, current state, and future prospects

(2009) Sung Ryeol Park et al.   APPLIED MICROBIOLOGY AND BIOTECHNOLOGY

CEM-101, a novel fluoroketolide: antimicrobial activity against a diverse collection of Gram-positive and Gram-negative bacteria

(2009) Shannon D. Putnam et al.   DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE

Antibiotics for Emerging Pathogens

(2009) M. A. Fischbach et al.   SCIENCE