Unveiling the Stereoselectivity Aspects of Metallaphotoredox Decarboxylative Arylation
Author:
Affiliation:
1. Small Molecule Discovery Chemistry, Bristol Myers Squibb Research and Early Development, Princeton, New Jersey 08543, United States
2. Chemical Process Development, Bristol Myers Squibb, New Jersey, New Brunswick 08901, United States
Funder
Bristol-Myers Squibb
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acscatal.4c03818
Reference60 articles.
1. Advances in Transition Metal (Pd,Ni,Fe)-Catalyzed Cross-Coupling Reactions Using Alkyl-organometallics as Reaction Partners
2. Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides and Pseudohalides
3. Pronounced Solvent Effect on the Hydrostannylation of Propargylic Alcohol Derivatives withnBu3SnH/Et3B at Room Temperature
4. Highly Stereo- and Regioselective Hydrostannylation of Internal Alkynes Promoted by Simple Boric Acid in Air
5. Highly Diastereoselective C(sp3)C(sp) Cross-Coupling Reactions between 1,3- and 1,4-Substituted Cyclohexylzinc Reagents and Bromoalkynes through Remote Stereocontrol
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