About: Recent Developments in the Field of β-Lactam Antibiotics

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description	article (en) ലേഖനം (ml) հոդված (hy) wetenschappelijk artikel (nl) artículu científicu espublizáu en 1985 (ast) наукова стаття, опублікована в березні 1985 (uk) im März 1985 veröffentlichter wissenschaftlicher Artikel (de) مقالة علمية نشرت في مارس 1985 (ar)
publication date	wds:Q36142943-A4366435-6BC5-4274-BD61-3748C760173F
publication date	1985-03-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q36142943-13531BF1-0739-44E6-A20B-720601EAA179 wds:Q36142943-1475B3CC-D5A1-4798-81BE-44398556B561 wds:Q36142943-29B1CB19-6AAC-4753-94A7-7E941B915D85 wds:Q36142943-2A4F3A08-68E1-4804-9628-1D763C9DB6FC wds:Q36142943-2B19F343-1E26-420D-B348-30B0FA635CB1 wds:Q36142943-41FFDD4A-230C-4179-8194-FE947BCC26A7 wds:Q36142943-659C1B01-B4EB-4A99-9141-1EA4F4E9BF44 wds:Q36142943-6E04AFD9-1530-4F90-A4F7-0D5A9E4EA832 wds:Q36142943-84D1EE6C-ED88-4AE8-8597-EBDA9BDD904B wds:Q36142943-B0A4D667-9FCA-469A-8802-D9C4A638BE69 wds:Q36142943-E0078CF7-A7F2-4998-8A2D-34D906A5721B wds:Q36142943-F13C1A8E-1A44-4E86-ACE5-ECD0DC6EE400 wds:Q36142943-F30630F1-E7EB-4912-A925-4928EF8453B9
cites work	Thienamycin, a new beta-lactam antibiotic. I. Discovery, taxonomy, isolation and physical properties Sulfazecin and isosulfazecin, novel beta-lactam antibiotics of bacterial origin Structures of olivanic acid derivatives MM22380, MM22381, MM22382 and MM22383; Four new antibiotics isolated from Streptomyces olivaceus Four further antibiotics related to olivanic acid produced by Streptomyces olivaceus: Fermentation, isolation, characterisation and biosynthetic studies. Nocardicin A, a new monocyclic beta-lactam antibiotic. I. Discovery, isolation and characterization Monocyclic beta-lactam antibiotics produced by bacteria The in vitro activity, human pharmacology, and clinical effectiveness of new beta-lactam antibiotics Chitinovorins A, B and C, novel beta-lactam antibiotics of bacterial origin PS-5, a new beta-lactam antibiotic from Streptomyces Olivanic acids, a family of .BETA.-lactam antibiotics with .BETA.-lactamase inhibitory properties produced by Streptomyces species. II. Isolation and characterisation of the olivanic acids MM 4550, MM 13902 and MM 17880 from Streptomyces olivaceus. Carpetimycins A and B, new beta-lactam antibiotics Microbiology: Proteins that bind the β-lactam antibiotics New -lactam antibiotics. Preparation of 7-aminocephalocillanic acid
author name string	wds:Q36142943-040223DE-092E-41A0-8F4F-155F8DBBFC72 wds:Q36142943-08872692-1BCE-4874-A917-DA816115E1EC wds:Q36142943-CCC39664-CF96-48C7-B6FC-1C448B1330ED wds:Q36142943-E6EE6E2B-DB35-433C-8097-D6F472A85DE2
author name string	Walter Dürckheimer Jürgen Blumbach Karl Heinz Scheunemann Rudolf Lattrell
rdfs:label	Recent Developments in the Field of β-Lactam Antibiotics (en) Recent Developments in the Field of β-Lactam Antibiotics (nl) Recent Developments in the Field of β-Lactam Antibiotics (ast)
skos:prefLabel	Recent Developments in the Field of β-Lactam Antibiotics (en) Recent Developments in the Field of β-Lactam Antibiotics (nl) Recent Developments in the Field of β-Lactam Antibiotics (ast)
name	Recent Developments in the Field of β-Lactam Antibiotics (en) Recent Developments in the Field of β-Lactam Antibiotics (nl) Recent Developments in the Field of β-Lactam Antibiotics (ast)
title	wds:Q36142943-3DBE16BC-FAE8-42A9-8655-0BF80565EEB8
title	Recent Developments in the Field of β-Lactam Antibiotics (en)
page(s)	wds:Q36142943-26EB50C0-3402-486C-8859-B44F8C61CC6D
page(s)	180-202
instance of	wds:Q36142943-9590C05E-D919-45E7-BAC7-718D3AF7F141
instance of	scholarly article
published in	wds:Q36142943-53A12EF8-BE35-4012-BC7D-BB375A76CA5F
published in	Angewandte Chemie. International edition in English
issue	wds:Q36142943-7621FF31-46CC-4C96-B5B2-E76D71116485
volume	wds:Q36142943-D166335A-C3E3-49DC-A123-35148EE04898
issue	3
volume	24
DOI	wds:Q36142943-74B36963-8C6B-4F4C-88C8-3F98081FB47E
DOI	http://dx.doi.org/10.1002/ANIE.198501801
DOI	10.1002/ANIE.198501801
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q36142943
is cites work of	β-Peptides: Synthesis by Arndt-Eistert homologation with concomitant peptide coupling. Structure determination by NMR and CD spectroscopy and by X-ray crystallography. Helical secondary structure of a β-hexapeptide in solution and its stability tow The enzymes of β-lactam biosynthesis Beta-lactamase inhibitors: evolving compounds for evolving resistance targets Isocyanate acting as a carbonyl precursor: pyridyl group-assisted formation of 4H-pyrido[1,2-a]pyrimidin-4-ones from ketimines and isocyanates Correlation of biological activity in β-lactam antibiotics with Woodward and Cohen structural parameters—a Cambridge database study Synthesis and biological activity of N-substituted-3-chloro-2-azetidinones. Application of a new chiral stationary phase containing the glycopeptide antibiotic A-40,926 in the direct chromatographic resolution of β-amino acids Studies on 3'-quaternary ammonium cephalosporins--III. Synthesis and antibacterial activity of 3'-(3-aminopyrazolium) cephalosporins Coordinating properties of the Cephalexine antibiotic. A potentiometric study of the complexes formation between Cephalexine and Co(II), Ni(II) and Cu(II) metal ions New fragmentation and rearrangement reactions of the azetidine ring promoted by AlEt2Cl Direct acyl substitution of carboxylic acids: a chemoselective O- to N-acyl migration in the traceless Staudinger ligation. Studies on stereoselective [2+2] cycloadditions between N,N-dialkylhydrazones and ketenes Asymmetric synthesis of α-keto β-lactams via [2+2] cycloaddition reaction: A concise approach to optically active (α-hydroxy β-lactams and β-alkyl(aryl)isoserines Hexacarbonyl dicobalt complexed N-pro-2-ynyl-2-azetidinones: a new entry to N-unsubstituted-β-lactams through a Nicholas-type reaction A rapid procedure to prepare cefotaxime 1,3-iminoketones as new synthons for the stereocontrolled preparation of useful carbapenem intermediates Biocatalytic production of bicyclic β-lactams with three contiguous chiral centres using engineered crotonases FTIR study of five complex beta-lactam molecules Stereoselective, Temperature-Dependent [2+2] Cycloaddition ofN,N-Dialkylhydrazones toN-Benzyl-N-(benzyloxycarbonyl)aminoketene
is cites work of	wds:Q46878441-C478406D-47B3-4B65-8FAC-A1ED01A031B8 wds:Q35906971-5E47E0C9-BBAD-4128-B952-014528B6796A wds:Q55889174-5DAED057-51D1-4D25-AFC3-4EE19B59775B wds:Q63386491-C1335612-BA84-41B8-AF4E-E73828561AF2 wds:Q34310470-ACF62C42-360C-44CE-8E59-343705129C4E wds:Q45130645-478C1E3D-3A18-4523-98A6-84C1BAF08D88 wds:Q57974622-5339F725-2D1C-4737-9792-5C42057A3DC9 wds:Q57673827-B8CA55EB-A33B-4472-A3A6-94E376B98F96 wds:Q63386527-B1C73D0B-3A26-41BC-8D53-B78BDF7E4030 wds:Q63353667-C7D9F77F-61B0-4B2E-8EF3-2109453993E3 wds:Q73253760-E02383E6-41F4-4AE9-9D5B-98D5BA7270A0

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