Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Peter Dinér"'
Publikováno v:
Communications Chemistry, Vol 5, Iss 1, Pp 1-8 (2022)
Photo-mediated radical dearomatization involving 5-exo-trig cyclizations has proven to be an important route to accessing spirocyclic compounds, whereas 6-exo-trig spirocyclization has been much less explored. Here, a dearomative annulation cascade i
Externí odkaz:
https://doaj.org/article/35635e17c8964fc3979cd50dce990aba
Publikováno v:
Molecules, Vol 19, Iss 9, Pp 14273-14291 (2014)
The development of new approaches to obtain optically pure β-hydroxy esters is an important area in synthetic organic chemistry since they are precursors of other high value compounds. Herein, the kinetic resolution of racemic β-hydroxy esters usin
Externí odkaz:
https://doaj.org/article/ce54411409f54776a8ca5ca8a3728c82
Publikováno v:
Micromachines, Vol 5, Iss 1, Pp 81-96 (2014)
We present a single cell study of a highly effective Hog1 inhibitor. For this application, we used sequential treatment of a Saccharomyces cerevisiae cell array, with the Hog1 inhibitor and osmotic stress. For this purpose, a four-inlet microfluidic
Externí odkaz:
https://doaj.org/article/87031ee8e83041a8af4d9db7dab289d2
Publikováno v:
Molecules, Vol 14, Iss 12, Pp 5124-5143 (2009)
A versatile method for the synthesis of chiral 1,4-disubstituted-1,2,3-triazole derivatives starting from easily accessible naturally occurring D-or L-amino acids as chiral synthons is described. The amino acids were converted into azido alcohols, fo
Externí odkaz:
https://doaj.org/article/4368f4b501f943ef9102215eab2b0dfc
Autor:
Peter Dinér, Jenny Veide Vilg, Jimmy Kjellén, Iwona Migdal, Terese Andersson, Marinella Gebbia, Guri Giaever, Corey Nislow, Stefan Hohmann, Robert Wysocki, Markus J Tamás, Morten Grøtli
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20012 (2011)
The Saccharomyces cerevisiae High-Osmolarity Glycerol (HOG) pathway is a conserved mitogen-activated protein kinase (MAPK) signal transduction system that often serves as a model to analyze systems level properties of MAPK signaling. Hog1, the MAPK o
Externí odkaz:
https://doaj.org/article/a6c56fb831774432b4965e9be714569f
Autor:
Gregory R. Alvey, Elena V. Stepanova, Andrey Shatskiy, Josefin Lantz, Rachel Willemsen, Alix Munoz, Peter Dinér, Markus D. Kärkäs
An efficient protocol for the asymmetric synthesis of unnatural amino acids is realized through photoredox-mediated C–O bond activation of oxalate esters derived from aliphatic alcohols as the radical precursors. The developed system uses chiral gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbe28960e6f6157dbf1c85057228ae1c
https://doi.org/10.26434/chemrxiv-2023-dnbpx
https://doi.org/10.26434/chemrxiv-2023-dnbpx
Publikováno v:
The Journal of Organic Chemistry
Sulfonimidamides (SIAs) and sulfoximines (SOIs) have attracted attention due to their potential in agriculture and in medicinal chemistry as bioisosteres of biologically active compounds, and new synthetic methods are needed to access and explore the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::968aebf8828da074f0ebe9ab2a2850be
https://doi.org/10.1021/acs.joc.1c02241
https://doi.org/10.1021/acs.joc.1c02241
Autor:
Elena V. Stepanova, Björn Blomkvist, Bhushan P. Kore, A. Z. Temerdashev, Peter Dinér, Jian-Quan Liu, Anton Axelsson, James M. Gardner, Andrey Shatskiy, Markus D. Kärkäs
Publikováno v:
Chemical Science
A protocol for stereoselective C-radical addition to a chiral glyoxylate-derived N-sulfinyl imine was developed through visible light-promoted photoredox catalysis, providing a convenient method for the synthesis of unnatural α-amino acids. The deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e71f141149d2279c87cff95c4beac34
https://doi.org/10.1039/d1sc00658d
https://doi.org/10.1039/d1sc00658d
Autor:
Peter Dinér, June Izquierdo, Aitor Landa, Jose M. Mercero, Noémie Demurget, Claudio Palomo, Mikel Oiarbide, Tore Brinck
Publikováno v:
Chemistry – A European Journal. 25:12431-12438
A bifunctional amine/squaramide catalyst promoted direct aldol addition of an hydantoin surrogate to pyridine 2-carbaldehyde N-oxides to afford adducts bearing two vicinal tertiary/quaternary carbons in high diastereo- and enantioselectivity (d.r. up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54ec3e3b501f43a51dc19dbb6e447448
https://doi.org/10.1002/chem.201902817
https://doi.org/10.1002/chem.201902817
Autor:
Peter Dinér, Björn Blomkvist
Publikováno v:
ChemistrySelect. 4:7431-7436
The combination of anline and tetrafluoroboric acid diethyl etherate (2.5 mol% and 5 mol%, respectively) significantly accelerates the formation of sulfinyl imines in dichloromethane and isopropyla ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e71b5ea1aa9aa774b4d742815391daeb
https://doi.org/10.1002/slct.201901218
https://doi.org/10.1002/slct.201901218