Novel azalides derived from 16-membered macrolides. III. Azalides modified at the C-15 and 4″ positions: Improved antibacterial activities

A Versatile Catalyst for Heck Reactions of Aryl Chlorides and Aryl Bromides under Mild Conditions

Adam F. Littke, Gregory C. Fu · Journal of the American Chemical Society · 2001 · 690 citations

Natural Sciences, Chemistry, Catalysis +14

A novel and efficient macrolactonization of ω-hydroxycarboxylic acids using 2-methyl-6-nitrobenzoic anhydride (MNBA)

Isamu Shiina, Mari Kubota, Ryoutarou Ibuka · Tetrahedron Letters · 2002 · 274 citations

Pharmacy, Medicinal Chemistry, Biocatalysis +3

Chemical modification of erythromycins. I. Synthesis and antibacterial activity of 6-O-methylerythromycins A.

Shigeo Morimoto, Yōko Takahashi, Yoshiaki Watanabe et al. · The Journal of Antibiotics · 1984 · 232 citations · Full text

Pharmacy, Chemistry, Medicinal Chemistry +14

Synthesis and antibacterial activity of HMR 3647 a new ketolide highly potent against erythromycin-resistant and susceptible pathogens

Alexis Denis, Constantin Agouridas, Jean-Michel Auger et al. · Bioorganic & Medicinal Chemistry Letters · 1999 · 195 citations

Pharmacy, Medicinal Chemistry, Pharmacology +13

Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3"-O-propionylleucomycin A5 (TMS-19-Q).

Hideo Sakakibara, OSAMU OKEKAWA, Tatsuro Fujiwara et al. · The Journal of Antibiotics · 1981 · 61 citations · Full text

Pharmacy, Chemistry, Medicinal Chemistry +12