Selective halogenation of pyridines using designed phosphine reagents
Halopyridines are key building blocks for synthesizing pharmaceuticals, agrochemicals, and ligands for metal complexes, but strategies to selectively halogenate pyridine C–H precursors are lacking. We designed a set of heterocyclic phosphines that are installed at the 4-position of pyridines as phos...
Autori principali: | Levy, JN, Alegre-Requena, JV, Liu, R, Paton, RS, McNally, A |
---|---|
Natura: | Journal article |
Lingua: | English |
Pubblicazione: |
American Chemical Society
2020
|
Documenti analoghi
Documenti analoghi
-
A pyridine–pyridine cross‐coupling reaction via dearomatized radical intermediates
di: Koniarczyk, JL, et al.
Pubblicazione: (2019) -
Unconventional reactivity of ethynylbenziodoxolone reagents and thiols: scope and mechanism
di: Liu, B, et al.
Pubblicazione: (2020) -
Nozaki-hiyama reactions on halogenated allylchromium reagents: A new entry for the preparation of quaternary halogenated carbons
di: Baati, R, et al.
Pubblicazione: (2000) -
The conformational analysis of phosphine ligands in organometallic complexes. Part 2. Triphenylphosphine coordinated to achiral and prochiral octahedral metal centres
di: Costello, J, et al.
Pubblicazione: (1999) -
Catalyst-Free Trans-Selective Oxyiodination and Oxychlorination of Alkynes Employing N–X (Halogen) Reagents
di: Jiaqiong Sun, et al.
Pubblicazione: (2023-11-01)