Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules

Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules

Reductive cross-electrophile transformations have recently been made into a robust and long-lasting synthetic technique for the production of specific C[sbnd]C bonds. The use of inexpensive and plentiful electrophiles eliminates the need for pre-formation and handling of organometallics. In stereosp...

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Published in:Journal of Saudi Chemical Society
Main Author: Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
Format: Review
Language:English
Published: Elsevier B.V. 2023
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146252728&doi=10.1016%2fj.jscs.2022.101589&partnerID=40&md5=dc1af534ec5dd2f5d2113c1bedef61a0
id 2-s2.0-85146252728
spelling 2-s2.0-85146252728
Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
2023
Journal of Saudi Chemical Society
27
1
10.1016/j.jscs.2022.101589
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146252728&doi=10.1016%2fj.jscs.2022.101589&partnerID=40&md5=dc1af534ec5dd2f5d2113c1bedef61a0
Reductive cross-electrophile transformations have recently been made into a robust and long-lasting synthetic technique for the production of specific C[sbnd]C 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. © 2022
Elsevier B.V.
13196103
English
Review
All Open Access; Gold Open Access
author Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
spellingShingle Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
author_facet Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
author_sort Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z.
title Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
title_short Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
title_full Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
title_fullStr Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
title_full_unstemmed Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
title_sort Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules
publishDate 2023
container_title Journal of Saudi Chemical Society
container_volume 27
container_issue 1
doi_str_mv 10.1016/j.jscs.2022.101589
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146252728&doi=10.1016%2fj.jscs.2022.101589&partnerID=40&md5=dc1af534ec5dd2f5d2113c1bedef61a0
description Reductive cross-electrophile transformations have recently been made into a robust and long-lasting synthetic technique for the production of specific C[sbnd]C 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. © 2022
publisher Elsevier B.V.
issn 13196103
language English
format Review
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
_version_ 1809678478813954048

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