| Semi-synthetic approaches to novel penicillins. | |
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MedLine Citation:
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PMID: 1891804 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The first part of this account of the discovery of penicillin, published in last month's issue of TIBS, concluded with the detection of 6-beta-amino-penicillanic acid (6-APA), the nucleus of the penicillin structure. The exploitation of 6-APA led to the preparation of a range of clinically important semi-synthetic penicillins, which is described in this article. |
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Authors:
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J H Nayler |
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Publication Detail:
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Type: Journal Article; Review |
Journal Detail:
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Title: Trends in biochemical sciences Volume: 16 ISSN: 0968-0004 ISO Abbreviation: Trends Biochem. Sci. Publication Date: 1991 Jun |
Date Detail:
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Created Date: 1991-10-15 Completed Date: 1991-10-15 Revised Date: 2005-11-16 |
Medline Journal Info:
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Nlm Unique ID: 7610674 Medline TA: Trends Biochem Sci Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 234-7 Citation Subset: IM |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Penicillins
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chemical synthesis* |
| Chemical | |
Reg. No./Substance:
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0/Penicillins |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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