Stereoselective Synthesis of the C(1)−C(19) Fragment of Tetrafibricin
Author:
Affiliation:
1. Departments of Chemistry and Biochemistry, Scripps Florida, Jupiter, Florida 33458
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0629869
Reference25 articles.
1. Tetrafibricin, a novel fibrinogen receptor antagonist. I. Taxonomy, fermentation, isolation, characterization and biological activities.
2. Tetrafibricin, a novel fibrinogen receptor antagonist. II. Structural elucidation.
3. Tetrafibricin Has a High Selectivity for GPIIb/IIIa: Comparison of the Effects of Tetrafibricin and RGDS on GPIIb/IIIa and the Vitronectin Receptor
4. Tetrafibricin: A nonpeptidic fibrinogen receptor inhibitor from Streptomyces neyagawaensis. (II) its antiplatelet activities
5. Complete Stereochemistry of Tetrafibricin
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