Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Andrew R. Ickes"'
Publikováno v:
Organic Process Research & Development. 27:423-447
This highlight is the second installment of a series of highlights on nonprecious-metal-catalyzed reactions of interest to the pharmaceutical industry. Selected transformations from March to June 2...
Autor:
Su Yu, Lakshmi Bhagavatula, Brian J. Kotecki, Travis B. Dunn, Eric G. Moschetta, Westin H. Morrill, Andrew R. Ickes, Troy Reynolds, James C. Marek, Michael J. Rozema, Alan Christesen, Michael Rasmussen, Mathew M. Mulhern
Publikováno v:
Organic Process Research & Development. 26:949-962
Autor:
Byung Joo Lee, Andrew R. Ickes, Anil K. Gupta, Seth C. Ensign, Tam D. Ho, Anika Tarasewicz, Evan P. Vanable, Gregory D. Kortman, Kami L. Hull
Publikováno v:
Org Lett
Vicinal diamines are a common motif found in biologically active molecules. The hydroamination of allyl amine derivatives is a powerful approach for the synthesis of substituted 1,2-diamines. Herein, the rhodium-catalyzed hydroamination of primary an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7fd92e73e1424b47692088918e5364c
https://europepmc.org/articles/PMC9757009/
https://europepmc.org/articles/PMC9757009/
Enabling Suzuki-Miyaura coupling of Lewis-basic arylboronic esters with a nonprecious metal catalyst
Autor:
Michael C. Haibach, Andrew R. Ickes, Sergei Tcyrulnikov, Shashank Shekhar, Sebastien Monfette, Rafal Swiatowiec, Brian J. Kotecki, Jason Wang, Amanda L. Wall, Rodger F. Henry, Eric C. Hansen
Publikováno v:
Chemical science. 13(43)
The high cost and negative environmental impact of precious metal catalysts has led to increased demand for nonprecious alternatives for widely practiced reactions such as the Suzuki-Miyaura coupling (SMC). Ni-catalyzed versions of this reaction have
Publikováno v:
Journal of the American Chemical Society. 136:11256-11259
The synthesis of 1,2-diamines via a Rh-catalyzed intermolecular hydroamination of N-allyl imines with cyclic amines is presented. Coordinating groups proximal to the olefin bind to the catalyst and promote the transformation. The reaction affords 1,2
Publikováno v:
ChemInform. 46
The synthesis of 1,2-diamines via a Rh-catalyzed intermolecular hydroamination of N-allyl imines with cyclic amines is presented. Coordinating groups proximal to the olefin bind to the catalyst and promote the transformation. The reaction affords 1,2