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- W4312182141 endingPage "101589" @default.
- W4312182141 startingPage "101589" @default.
- W4312182141 abstract "Reductive cross-electrophile transformations have recently been made into a robust and long-lasting synthetic technique for the production of specific CC 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." @default.
- W4312182141 created "2023-01-04" @default.
- W4312182141 creator A5023800408 @default.
- W4312182141 creator A5026801674 @default.
- W4312182141 creator A5028332715 @default.
- W4312182141 creator A5042650517 @default.
- W4312182141 creator A5044193886 @default.
- W4312182141 creator A5068196582 @default.
- W4312182141 date "2023-01-01" @default.
- W4312182141 modified "2023-09-25" @default.
- W4312182141 title "Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules" @default.
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