An article General Paradigm in Photoredox Nickel-Catalyzed Cross-Coupling Allows for Light-Free Access to Reactivity WOS:000522777500001 published article about MONOPHOSPHINE LIGANDS; OXIDATIVE ADDITION; ARYL HALIDES; ELECTROPHILES; COMPLEXES; AMINATION; MECHANISM in [Sun, Rui; Qin, Yangzhong; Nocera, Daniel G.] Harvard Univ, Dept Chem & Chem Biol, 12 Oxford St, Cambridge, MA 02138 USA in 2020, Cited 68. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Formula: C8H8O2
Self-sustained Ni-I/III cycles are established as a potentially general paradigm in photoredox Ni-catalyzed carbon-heteroatom cross-coupling reactions through a strategy that allows us to recapitulate photoredox-like reactivity in the absence of light across a wide range of substrates in the amination, etherification, and esterification of aryl bromides, the latter of which has remained, hitherto, elusive under thermal Ni catalysis. Moreover, the accessibility of esterification in the absence of light is especially notable because previous mechanistic studies on this transformation under photoredox conditions have unanimously invoked energy-transfer-mediated pathways.
Formula: C8H8O2. Welcome to talk about 99-93-4, If you have any questions, you can contact Sun, R; Qin, YZ; Nocera, DG or send Email.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles