I agree that this site is using cookies. You can find further informations here.
X
Gabbey, Alexis L.
9  results:
Search for persons X
?
1

Ni-Catalyzed Reductive 1,2-Alkylarylation of Alkenes for th..:

Pearson, James W. ; Hou, Teh Ren ; Golijanin, Jelena...
Organic Letters.  26 (2024)  26 - p. 5560-5565 , 2024
Link: https://doi.org/10.1021/..
 
?
2

Synthesis of Borylated (Aminomethyl)cyclopropanes Using C1–..:

McDonald, Tyler R. ; Turner, Julia A. ; Gabbey, Alexis L...
Organic Letters.  26 (2024)  18 - p. 3822-3827 , 2024
Link: https://doi.org/10.1021/..
 
?
3

Nickel-Catalyzed Reductive Arylation of Redox Active Esters..:

Michel, Nicholas W. M. ; Gabbey, Alexis L. ; Edjoc, Racquel K....
The Journal of Organic Chemistry.  , 2024
Link: https://doi.org/10.1021/..
 
?
4

Metal-catalysed C–C bond formation at cyclopropanes:

Gabbey, Alexis L. ; Scotchburn, Katerina ; Rousseaux, Sophie A. L.
Nature Reviews Chemistry.  7 (2023)  8 - p. 548-560 , 2023
Link: https://doi.org/10.1038/..
 
?
5

Ni-Catalyzed Reductive Cross-Coupling of Cyclopropylamines ..:

West, Michael S. ; Gabbey, Alexis L. ; Huestis, Malcolm P..
Organic Letters.  24 (2022)  45 - p. 8441-8446 , 2022
Link: https://doi.org/10.1021/..
 
?
6

Synthesis of α-Aryl Secondary Amides via Nickel-Catalyzed R..:

Gabbey, Alexis L. ; Michel, Nicholas W. M. ; Hughes, Jonathan M. E...
Organic Letters.  24 (2022)  17 - p. 3173-3178 , 2022
Link: https://doi.org/10.1021/..
 
?
7

Enantioselective Tertiary Electrophile (Hetero)Benzylation:..:

Doyle, Michael G. J. ; Gabbey, Alexis L. ; McNutt, Wesley.
Angewandte Chemie.  133 (2021)  51 - p. 26699-26703 , 2021
Link: https://doi.org/10.1002/..
 
?
8

Enantioselective Tertiary Electrophile (Hetero)Benzylation:..:

Doyle, Michael G. J. ; Gabbey, Alexis L. ; McNutt, Wesley.
Angewandte Chemie International Edition.  60 (2021)  51 - p. 26495-26499 , 2021
Link: https://doi.org/10.1002/..
 
?
9

Nickel-Catalyzed Reductive Arylation of Redox Active Esters..:

Nicholas W. M. Michel ; Alexis L. Gabbey ; Racquel K. Edjoc...
doi:10.1021/acs.joc.3c02354.s001.  , 1753
Link: https://doi.org/10.1021/..
 
1-9