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...
| 發表在: | Journal of Saudi Chemical Society |
|---|---|
| 主要作者: | |
| 格式: | Review |
| 語言: | English |
| 出版: |
Elsevier B.V.
2023
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| 在線閱讀: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85146252728&doi=10.1016%2fj.jscs.2022.101589&partnerID=40&md5=dc1af534ec5dd2f5d2113c1bedef61a0 |
| id |
Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z. |
|---|---|
| spelling |
Afzal U.; Bilal M.; Zubair M.; Rasool N.; Adnan Ali Shah S.; Amiruddin Zakaria Z. 2-s2.0-85146252728 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 |
2-s2.0-85146252728 |
| spellingShingle |
2-s2.0-85146252728 Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules |
| author_facet |
2-s2.0-85146252728 |
| author_sort |
2-s2.0-85146252728 |
| 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_ |
1828987866614595584 |