Reductive Hydrolysis of the 59,60-Amide Bond of Teicoplanin Antibiotics: A Key Step from Natural to Synthetic Glycopeptides
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| Veröffentlicht in: | Journal of medicinal chemistry 1994-09, Vol.37 (19), p.2988-2990 |
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| Format: | Artikel |
| Sprache: | eng |
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| container_end_page | 2990 |
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| container_issue | 19 |
| container_start_page | 2988 |
| container_title | Journal of medicinal chemistry |
| container_volume | 37 |
| creator | Malabarba, Adriano Ciabatti, Romeo |
| description | |
| doi_str_mv | 10.1021/jm00045a002 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 0022-2623 |
| ispartof | Journal of medicinal chemistry, 1994-09, Vol.37 (19), p.2988-2990 |
| issn | 0022-2623 1520-4804 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_76753270 |
| source | MEDLINE; ACS Publications |
| subjects | Amides - chemistry Amino Acid Sequence Carbohydrate Sequence Chemistry Exact sciences and technology Glycopeptides - chemical synthesis Glycopeptides - chemistry Hydrolysis Molecular Sequence Data Organic chemistry Oxidation-Reduction Peptides Preparations and properties Structure-Activity Relationship Teicoplanin - chemical synthesis Teicoplanin - chemistry |
| title | Reductive Hydrolysis of the 59,60-Amide Bond of Teicoplanin Antibiotics: A Key Step from Natural to Synthetic Glycopeptides |
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