
AbstractIn search for new antibiotics we replaced the amide moiety of lincomycin 1 by a 1,2,3‐triazole ring. The 1,2,3‐triazoles 10a–10k were obtained as single regioisomers by ‘click reaction’ of azide 5 with the alkyne 9k, derived from propyl hygric acid, and the alkyl, aryl, or cycloalkyl alkynes ribosomes 9a–9j. The new analogues proved inactive towards wild‐type and A2058G mutant.
1303 Biochemistry, 10179 Institute of Medical Microbiology, 1503 Catalysis, 1604 Inorganic Chemistry, 3002 Drug Discovery, Organic Chemistry, 610 Medicine & health, Biochemistry, Catalysis, Inorganic Chemistry, Drug Discovery, 570 Life sciences; biology, Physical and Theoretical Chemistry, 1606 Physical and Theoretical Chemistry, 1605 Organic Chemistry
1303 Biochemistry, 10179 Institute of Medical Microbiology, 1503 Catalysis, 1604 Inorganic Chemistry, 3002 Drug Discovery, Organic Chemistry, 610 Medicine & health, Biochemistry, Catalysis, Inorganic Chemistry, Drug Discovery, 570 Life sciences; biology, Physical and Theoretical Chemistry, 1606 Physical and Theoretical Chemistry, 1605 Organic Chemistry
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 23 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
