Uzma Afzal and Muhammad Bilal and Muhammad Zubair and Nasir Rasool and Syed Adnan Ali Shah and Zainul Amiruddin Zakaria (2023) Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules. Journal of Saudi Chemical Society, 27. pp. 1-45. ISSN 1319-6103
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Abstract
Reductive cross-electrophile transformations have recently been made into a robust and long-lasting synthetic technique for the production of specific CAC bonds. The use of inexpensive and plentiful electrophiles eliminates the need for pre-formation and handling of organometallics. In stereospecific reductive cross-coupling, nickel is one of the most cost-effective and flexible transition metals. This paper examines current developments in nickel catalyzed reductive cross coupling reactions and their potential application for the synthesis of biologically active molecules over the previous nine years.
Item Type: | Article |
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Keyword: | Reductive, Cross-coupling, Electrophile, Bioactive |
Subjects: | Q Science > QD Chemistry > QD1-999 Chemistry > QD450-801 Physical and theoretical chemistry R Medicine > RC Internal medicine > RC31-1245 Internal medicine |
Department: | FACULTY > Faculty of Medicine and Health Sciences |
Depositing User: | SITI AZIZAH BINTI IDRIS - |
Date Deposited: | 02 May 2024 16:47 |
Last Modified: | 02 May 2024 16:47 |
URI: | https://eprints.ums.edu.my/id/eprint/38603 |
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