Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Isabelle N.-M. Leibler"'
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81092c9fd7c9dd3a9790cfe7dbcda508
https://doi.org/10.1002/047084289x.rn02417
https://doi.org/10.1002/047084289x.rn02417
Autor:
Molly S. Costanza-Robinson, Nicholas S. Caminiti, Sarah B. Nodder, Bryan Holtzman, Michael L Martini, Jacob A. Fox, Isabelle N.-M. Leibler, Madison B. Goodstein, Zitong B. Jia, Richard C. Bunt, Gina Mendolia, Eric T. Roberts, Staci A. Hill
Publikováno v:
Tetrahedron Letters. 58:432-436
A nucleophile crossover experiment was used to monitor the reversibility of nucleophilic addition of benzylamine to π-allylpalladium complexes. Dppe, dppp, dppb, and PHOX showed more crossover than PPh 3 and dppm in both DMF and dichloromethane. Cro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e31546566c61c2707b5c7739e025ef19
https://doi.org/10.1016/j.tetlet.2016.12.049
https://doi.org/10.1016/j.tetlet.2016.12.049
Autor:
Madison B. Goodstein, Nathaniel C. Nelson, Michael L Martini, Isabelle N.-M. Leibler, Zitong B. Jia, Bryan Holtzman, Richard C. Bunt, Nicholas S. Caminiti
Publikováno v:
Tetrahedron Letters. 56:5445-5448
Palladium-catalyzed allylic amination is an important synthetic reaction that is also frequently used as a benchmark for the design and evaluation of new chiral ligands. The effect of reversible nucleophilic addition on the reaction of benzylamine wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5431e28f07d82e113f29867254ba821a
https://doi.org/10.1016/j.tetlet.2015.08.010
https://doi.org/10.1016/j.tetlet.2015.08.010