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...
Egile Nagusiak: | Levy, JN, Alegre-Requena, JV, Liu, R, Paton, RS, McNally, A |
---|---|
Formatua: | Journal article |
Hizkuntza: | English |
Argitaratua: |
American Chemical Society
2020
|
Antzeko izenburuak
-
A pyridine–pyridine cross‐coupling reaction via dearomatized radical intermediates
nork: Koniarczyk, JL, et al.
Argitaratua: (2019) -
Unconventional reactivity of ethynylbenziodoxolone reagents and thiols: scope and mechanism
nork: Liu, B, et al.
Argitaratua: (2020) -
Nozaki-hiyama reactions on halogenated allylchromium reagents: A new entry for the preparation of quaternary halogenated carbons
nork: Baati, R, et al.
Argitaratua: (2000) -
The conformational analysis of phosphine ligands in organometallic complexes. Part 2. Triphenylphosphine coordinated to achiral and prochiral octahedral metal centres
nork: Costello, J, et al.
Argitaratua: (1999) -
Catalyst-Free Trans-Selective Oxyiodination and Oxychlorination of Alkynes Employing N–X (Halogen) Reagents
nork: Jiaqiong Sun, et al.
Argitaratua: (2023-11-01)