Titlebook: Recent Progress in the Chemical Synthesis of Antibiotics; G. Lukacs (Directeur de Recherche C.N.R.S.),M. Ohn Book 1990 Springer-Verlag Ber

大包裹

Recent Progress in the Chemical Synthesis of Antibiotics

間諜活動

暫時休息

Recent Progress in the Chemical Synthesis of Antibiotics978-3-642-75617-7

木質(zhì)

Jean-Marie Beau of works will be of interest to students and academics of Environment Studies, Human Geography and Environmental Policy, and will be of particular relevance to those involved in risk research and managing risk978-3-030-09734-9978-3-319-65211-5

tooth-decay

J. M. Paris,J. C. Barrière,C. Smith,P. E. Bost of works will be of interest to students and academics of Environment Studies, Human Geography and Environmental Policy, and will be of particular relevance to those involved in risk research and managing risk978-3-030-09734-9978-3-319-65211-5

obstinate

船員

The Chemistry of Pristinamycins,s have been devoted to semi-synthetic modification of these compounds for reasons of chemical instability; lack of, or large reductions in biological activity of simple transformation products; and up to the appearance of high-field NMR there was no efficient analytical method for structure confirmation of pristinamycin derivatives.

盡責(zé)

Nucleosides: Potential Drugs for AIDS Therapy,β′-fluoronucleosides, 2′,3′-dideoxy-3′-.-substituted nucleosides, 2′,3′-dideoxy-β-.-glycero-pent-2- enofuranosyl nucleosides, 2′,3′-dideoxynucleosides and carbocyclic, acyclic and .-nucleosides. Structure-activity relationships are also considered.

狂怒

Total Synthesis of Polyether Antibiotics, glucals, in the order of . + (.)by the sulfone carbanion method. The first convergent asymmetric synthesis of . was completed through the synthesis and aldol coupling of the C.-C. (.) and C.-C. (.) synthons. Coupling of C.-C. (.) and C.-C. (.) fragments followed by aldol condensation with С.-С. aldehyde (.) gave ..

Abominate

,Synthetic Aspects of Monocyclic β-Lactam Antibiotics,is review focusses on recent advances in the chemistry of the monocyclic β-lactams with particular attention to methods for the synthesis of enantiomerically pure azetidinones via the use of chiral starting materials or asymmetric induction. The literature from 1983 through early 1989 is discussed.