Processes of 1,3-Dipolar cycloaddition in nucleoside, nucleotide and bio conjugation and its importance in medicinal chemistry
Joint Authors
Abbas, Sahar Fadil
Karim, Asil Fadil
Mubarak, Hayfa A.
Ulwan, Hamid Husayn
Source
al-Kufa University Journal for Biology
Issue
Vol. 15, Issue 1 (31 Mar. 2023), pp.35-44, 10 p.
Publisher
University of Kufa Faculty of Science Department of live Sciences
Publication Date
2023-03-31
Country of Publication
Iraq
No. of Pages
10
Main Subjects
Abstract EN
In the 1,3-dipolar cycloaddition, a 1,3-dipole and a dipolarophile interact chemically to produce a five-membered ring.
The Huisgen cycloaddition occurs when an organic azide and an alkyne unite to form a 1,3-dipolar cycloaddition that results in a 1,2,3-triazole.
1,3-dipolar cycloaddition is an essential step in the regio- and stereoselective synthesis of five-membered heterocycles and their ring-opened acyclic derivatives.
Some of the cycloadducts produced by these reactions were converted into enantiopure precursors known to exist in some biologically active chemicals as well as an active stereoisomer of a pine sawfly sex pheromone.
The synthesis of several new enantiopure organocatalysts that were shown to be helpful in some The synthetic utility of these 1,3-dipolar cycloaddition processes with nitrones and a,b-unsaturated aldehydes was further demonstrated.
There are times when these reactions have modest to moderate diastereofacial selectivity.
the choose actual and nonracemic have improved.
Compound collections are created in chemical biology research using the BIOS concept, which draws its inspiration from natural product scaffolds.
In BIOS, the primary criterion utilized to develop hypotheses for the design and synthesis of targeted chemical libraries is biological relevance.
Because they outline the chemical domains that nature has explored, the underlying scaffolds of natural product classes in particular serve as an inspiration for BIOS because they can be thought of as "trivet can often be achieved if both the azomethine ylide and the dipolarophile are chi privileged.
American Psychological Association (APA)
Karim, Asil Fadil& Abbas, Sahar Fadil& Mubarak, Hayfa A.& Ulwan, Hamid Husayn. 2023. Processes of 1,3-Dipolar cycloaddition in nucleoside, nucleotide and bio conjugation and its importance in medicinal chemistry. al-Kufa University Journal for Biology،Vol. 15, no. 1, pp.35-44.
https://search.emarefa.net/detail/BIM-1495339
Modern Language Association (MLA)
Karim, Asil Fadil…[et al.]. Processes of 1,3-Dipolar cycloaddition in nucleoside, nucleotide and bio conjugation and its importance in medicinal chemistry. al-Kufa University Journal for Biology Vol. 15, no. 1 (2023), pp.35-44.
https://search.emarefa.net/detail/BIM-1495339
American Medical Association (AMA)
Karim, Asil Fadil& Abbas, Sahar Fadil& Mubarak, Hayfa A.& Ulwan, Hamid Husayn. Processes of 1,3-Dipolar cycloaddition in nucleoside, nucleotide and bio conjugation and its importance in medicinal chemistry. al-Kufa University Journal for Biology. 2023. Vol. 15, no. 1, pp.35-44.
https://search.emarefa.net/detail/BIM-1495339
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 44
Record ID
BIM-1495339