Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Hiromu Hattori"'
Publikováno v:
Organic Letters. 21:3456-3459
The unique 18-membered macrocyclic natural product mangrolide D was prepared in totally synthetic form. Key steps feature an Au-catalyzed glycosylation, aza-Michael addition, and LaLi3tris(binaphthoxide) catalyzed epoxidation. Detailed analysis of th
Autor:
Joel Roesslein, Daniel Ritz, Katja Zerbe, Georg Rueedi, Karl Gademann, Patrick Caspers, Hideki Miyatake-Ondozabal, Hiromu Hattori
Publikováno v:
Angewandte Chemie. 130:11186-11190
The macrocyclic antibiotic mangrolide A has been described to exhibit potent activity against a number of clinically important Gram-negative pathogens. Reported is the first enantioselective total synthesis of mangrolide A and derivatives. Salient fe
Publikováno v:
The Journal of organic chemistry. 83(13)
The commercial macrolide antibiotic fidaxomicin was synthesized in a highly convergent manner. Salient features of this synthesis include a β-selective noviosylation, a β-selective rhamnosylation, a ring-closing metathesis, a Suzuki coupling, and a
Autor:
Hiromu Hattori
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 76:1358-1359
Publikováno v:
Organic Letters
Org. Lett.
Org. Lett.
The first enantioselective total synthesis of fidaxomicin, also known as tiacumicin B or lipiarmycin A3, is reported. This novel glycosylated macrolide antibiotic is used in the clinic for the treatment of Clostridium difficile infections. Key featur