Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Samantha A. M. Smith"'
Publikováno v:
IUCrData, Vol 2, Iss 3, p x170452 (2017)
In the title compound, trans-(S,S)-[FeBr(CO)(PPh2CH2CH2NHCHPhCHPhNCHCH2PCy2)]BPh4, the FeII ion is in a distorted octahedral complex geometry with a cis-β ligand geometry in which two diastereomers co-crystallized in the asymmetric unit. These diast
Externí odkaz:
https://doaj.org/article/67e2c5a6057a443c94570497792df5a6
Autor:
Matthew V. Gradiski, Robert H. Morris, Brian T. H. Tsui, Chris S. G. Seo, Samantha A. M. Smith
Publikováno v:
Catalysis Science & Technology. 11:3153-3163
The use of manganese in homogeneous hydrogenation catalysis has been a recent focus in the pursuit of more environmentally benign base metal catalysts. It has great promise with its unique reactivity when coupled with metal–ligand cooperation of am
Autor:
Samantha A. M. Smith, Matthew V. Gradiski, Alan J. Lough, Maegan S. E. Ong, Ali Nemati Kharat, Robert H. Morris
Publikováno v:
Inorganic chemistry. 59(15)
The synthesis and use of the first examples of unsymmetrical, mixed phosphine donor tripodal NPP2' ligands N(CH2CH2PR2)2(CH2CH2PPh2) are presented. The ligands are synthesized via a convenient, one pot reductive amination using 2-(diphenylphosphino)e
Publikováno v:
Israel Journal of Chemistry. 57:1204-1215
The asymmetric transfer hydrogenation (ATH) of ketones is an efficient method for producing enantio-enriched alcohols which are used as intermediates in a variety of industrial processes. Here we report the synthesis of new iron ATH precatalysts (S,S
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (18), pp.12040-12049. ⟨10.1021/acs.joc.9b01964⟩
Journal of Organic Chemistry, 2019, 84 (18), pp.12040-12049. ⟨10.1021/acs.joc.9b01964⟩
Journal of Organic Chemistry, American Chemical Society, 2019, 84 (18), pp.12040-12049. ⟨10.1021/acs.joc.9b01964⟩
Journal of Organic Chemistry, 2019, 84 (18), pp.12040-12049. ⟨10.1021/acs.joc.9b01964⟩
International audience; Chiral amines are key building blocks in synthetic chemistry with numerous applications in the agricultural and pharmaceutical industries. Asymmetric imine hydrogenation, particularly with iridium catalysts, is well developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85c4af1d8fe5c0b4c854f5e058b91c6e
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02473966
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02473966
Autor:
Samantha A. M. Smith, Robert H. Morris
Publikováno v:
Synthesis. 47:1775-1779
A new iron(II)(Ph2P–NH–N–PCy2) complex with a dicyclohexylphosphino group trans to the NH group was found to catalyze the asymmetric transfer hydrogenation of a variety of ketones with high enantioselectivity.
Publikováno v:
Ligand Design in Metal Chemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f9dd9e477e76947a77be76dbe73f4c0
https://doi.org/10.1002/9781118839621.ch8
https://doi.org/10.1002/9781118839621.ch8
Publikováno v:
Angewandte Chemie. 124:2826-2829
There and back again: hydrogenation of esters and the reverse reaction of dehydrogenative coupling of alcohols are efficiently catalyzed by dimeric complexes of Ru and Os under neutral conditions. The Os dimer is an outstanding catalyst for the hydro
Autor:
Robert H. Morris, Samantha A. M. Smith
Publikováno v:
ChemInform. 46
A new iron(II)(Ph2P–NH–N–PCy2) complex with a dicyclohexylphosphino group trans to the NH group was found to catalyze the asymmetric transfer hydrogenation of a variety of ketones with high enantioselectivity.