Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gregory D. Kortman"'
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/
Autor:
An T. Ho, Seth C. Ensign, Evan P. Vanable, David Portillo, Jenna N. Humke, Gregory D. Kortman, Kami L. Hull
Publikováno v:
ACS Catal
An Ir-catalyzed regioselective hydroamination of allyl amines using aryl amines and catalyst-controlled regiodivergent hydroamination of allylic and homoallylic amines with aniline nucleophiles are reported. The directed hydroamination reactions affo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad5cf151d0f77691d7cd3b894aa40c4d
https://europepmc.org/articles/PMC10156092/
https://europepmc.org/articles/PMC10156092/
Autor:
Gregory D. Kortman, Kami L. Hull
Publikováno v:
ACS Catalysis. 7:6220-6224
The copper-catalyzed hydroarylation of internal, unsymmeric alkynes is presented. Trisubstituted alkenes are obtained as single diastereomers in good to excellent yields and excellent regioselectivities. The scope of the reaction is presented with re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ef5dbb26c0aaf3a541fed2295bb441f
https://doi.org/10.1021/acscatal.7b01847
https://doi.org/10.1021/acscatal.7b01847
Publikováno v:
Journal of the American Chemical Society. 138:11914-11919
The regiodivergent Rh-catalyzed hydrothiolation of allyl amines and imines is presented. Bidentate phosphine ligands with larger natural bite angles (βn ≥ 99°), for example, DPEphos, dpph, or L1, promote a Markovnikov-selective hydrothiolation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623f3d8649f4ec29da569155ac2fd069
https://doi.org/10.1021/jacs.6b07142
https://doi.org/10.1021/jacs.6b07142
Publikováno v:
Organometallics. 35:1713-1725
Titanocene–oxo complexes of the type Cpx2Ti═O(L) (Cpx = pentamethylcyclopentadienyl; tetramethylcyclopentadienyl; L = pyridine or derivatives) are synthesized from the corresponding titanocene–ethylene complexes via oxidation with pyridine N-ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2df45b2de55260b2368499fb5fe0304f
https://doi.org/10.1021/acs.organomet.6b00111
https://doi.org/10.1021/acs.organomet.6b00111
Publikováno v:
ChemInform. 47
The development of an anti-Markovnikov-selective hydroamination of unactivated alkenes is a significant challenge in organometallic chemistry. Herein, we present the rhodium-catalyzed anti-Markovnikov-selective hydroamination of homoallylic amines. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e189a80a0901ff712c4dd8c49e6a35d
https://doi.org/10.1002/chin.201617180
https://doi.org/10.1002/chin.201617180
Publikováno v:
Journal of the American Chemical Society. 137(43)
The development of an anti-Markovnikov-selective hydroamination of unactivated alkenes is a significant challenge in organometallic chemistry. Herein, we present the rhodium-catalyzed anti-Markovnikov-selective hydroamination of homoallylic amines. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a5b8d2ffdf6a9a84f4a1d7e3ca7e36
https://pubmed.ncbi.nlm.nih.gov/26456593
https://pubmed.ncbi.nlm.nih.gov/26456593
Publikováno v:
Synthesis; 2016, Vol. 48 Issue 5, pA44-A46, 3p