A total synthesis of the naturally occurring pyrrolo[2,3-]pyrimidine nucleoside, mycalisine A
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Bioactive marine metabolites IX. Mycalisines A and B, novel nucleosides which inhibit cell division of fertilized starfish eggs, from the marine sponge sp.
2. “Nucleoside Antibiotics” in Handbook of Biochemistry and Molecular Biology;Townsend,1975
3. SYNTHESIS, CHEMICAL REACTIVITY, AND CHEMOTHERAPEUTIC ACTIVITY OF CERTAIN SELENONUCLEOSIDES AND NUCLEOSIDES RELATED TO THE PYRROLO[2,3-d]PYRIMIDINE NUCLEOSIDE ANTIBIOTICS
4. Pyrrolopyrimidine nucleosides. 18, Synthesis and chemotherapeutic activity of 4-amino-7-(3-deoxy-.beta.-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide (3'-deoxysangivamycin) and 4-amino-7-(2-deoxy-.beta.-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carboxamide (2'-deoxysangivamycin)
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1. Total Synthesis of Mycalisine B;Marine Drugs;2019-04-14
2. Formation of Alkenes by Elimination;Comprehensive Organic Transformations;2018-02-28
3. Multicomponent Strategy for the Preparation of Pyrrolo[1,2-a]pyrimidine Derivatives under Catalyst-Free and Microwave Irradiation Conditions;Chinese Journal of Chemistry;2016-05-19
4. Annelation of pyrrolo[1,2-a]pyrimidine and pyrido[1,2-a]pyrimidine systems to a pyrazolopyridine framework by a cascade of two cyclization reactions;Tetrahedron Letters;2015-05
5. Porifera (Sponges)-5;Encyclopedia of Marine Natural Products;2014-08-07
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