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dc.contributor.authorPrusov, Evgeny V
dc.date.accessioned2013-05-30T14:23:41Z
dc.date.available2013-05-30T14:23:41Z
dc.date.issued2013-04
dc.identifier.citationTotal synthesis of antibiotics: recent achievements, limitations, and perspectives. 2013, 97 (7):2773-95 Appl. Microbiol. Biotechnol.en_GB
dc.identifier.issn1432-0614
dc.identifier.pmid23435901
dc.identifier.doi10.1007/s00253-013-4757-5
dc.identifier.urihttp://hdl.handle.net/10033/293089
dc.description.abstractSeveral recently accomplished total syntheses of antibiotic natural products were summarized in this review in order to present current trends in this area of research. Compounds from different substance classes, including polyketide, depsipeptide, polyketide-polypeptide hybrid, and saccharide, were chosen to demonstrate the advancement in both chemical methodology and corresponding synthetic strategy.
dc.language.isoenen
dc.rightsArchived with thanks to Applied microbiology and biotechnologyen_GB
dc.titleTotal synthesis of antibiotics: recent achievements, limitations, and perspectives.en
dc.typeArticleen
dc.contributor.departmentHelmholtz Zentrum für Infektionsforschung, Braunschweig, Germany. Evgeny.Prusov@helmholtz-hzi.deen_GB
dc.identifier.journalApplied microbiology and biotechnologyen_GB
refterms.dateFOA2018-06-13T21:22:48Z
html.description.abstractSeveral recently accomplished total syntheses of antibiotic natural products were summarized in this review in order to present current trends in this area of research. Compounds from different substance classes, including polyketide, depsipeptide, polyketide-polypeptide hybrid, and saccharide, were chosen to demonstrate the advancement in both chemical methodology and corresponding synthetic strategy.


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