Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Gregor Urbanietz"'
Autor:
Jennifer Albaneze-Walker, Gregor Urbanietz, Andras Horvath, Stefano Lancianesi, Alejandro Gimenez Molina, Thomas De Vijlder, Mattijs Baeten, Martine Canters
Publikováno v:
The Journal of organic chemistry. 87(19)
Azido nucleosides couple with phosphoramidites via an initial iminophosphorane, which eliminates acrylonitrile to generate the coupled dimer P(V) product. The vulnerable phosphite triester intermediate is bypassed entirely, making the methodology ver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca3f94cb9f0cdeeabe6514bfa045fa6
https://pubmed.ncbi.nlm.nih.gov/36161801
https://pubmed.ncbi.nlm.nih.gov/36161801
Autor:
Min Chul Kwon, Olivier Querolle, Xuedong Dai, Jan Willem Thuring, Tinne Verhulst, Ann Marien, Dries Goffin, Wei Cai, Vikki Keersmaekers, Filmon Eyassu, Karin Verstraeten, Sara El Ashkar, Shanna M Hogeling, Frank Jacob, Petra Vinken, Nicolas Darville, Vineet Pande, Daniel Krosky, Gregor Urbanietz, Bie Verbist, Lucille A. Ferrante, Christina Diane Drenberg, David Wilson, Ricardo M. Attar, Jan Jacob Schuringa, Nikki Daskalakis, Kathryn Packman, Christine Pietsch, Yusri Elsayed, Ulrike Philippar
Publikováno v:
Blood. 140:5928-5929
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc637fd2b48b32c40a713ec792434dbb
https://doi.org/10.1182/blood-2022-168921
https://doi.org/10.1182/blood-2022-168921
Publikováno v:
Synthesis : journal of synthetic organic chemistry 46(9), 1261-1269 (2014). doi:10.1055/s-0033-1340826
Synthesis : journal of synthetic organic chemistry 46(9), 1261-1269 (2014). doi:10.1055/s-0033-1340826
Published by Thieme, Stuttgart
Published by Thieme, Stuttgart
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9c5c5028abd74c7d2604a7eab20719f
https://doi.org/10.1055/s-0033-1340826
https://doi.org/10.1055/s-0033-1340826
Publikováno v:
Advanced Synthesis & Catalysis. 354:1481-1488
The asymmetric organocatalytic one-pot synthesis of polyfunctionalized cyclohexanes is described. Starting from β-keto esters, nitroalkenes and α,β-unstaturated aldehydes and employing a bifunctional norephedrine-based thiourea catalyst, six conti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd5383b67ac388198fa582760743c59e
https://doi.org/10.1002/adsc.201200120
https://doi.org/10.1002/adsc.201200120
Publikováno v:
Synthesis. 44:773-782
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a83bb771a9273310e94d9520fd86250e
https://doi.org/10.1055/s-0031-1289683
https://doi.org/10.1055/s-0031-1289683
Publikováno v:
Synthesis. 2011:1905-1911
A one-pot thiourea-catalyzed enantioselective synthesis of polyfunctionalized 4H-chromenes via a domino Michael-hemiacetalization reaction and subsequent dehydration is reported. Starting from 2-nitrovinylphenols and β-keto esters, the new protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c47156f1f571f4e08118589556c79ad
https://doi.org/10.1055/s-0030-1260017
https://doi.org/10.1055/s-0030-1260017
Publikováno v:
Chemical communications : ChemComm 50(52), 6853-6855 (2014). doi:10.1039/C4CC01885K
A highly stereoselective one-pot procedure involving an enantioselective Michael addition promoted by low loading of an amino-squaramide catalyst followed by an achiral base catalyzed domino Michael–Knoevenagel-type 1,2-addition sequence provides e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e642e15cdf36d859dddf0a3b396487
https://doi.org/10.1039/c4cc01885k
https://doi.org/10.1039/c4cc01885k
Publikováno v:
ChemInform. 45
Starting from α-hydroxymethyl nitroalkenes and various 1,3-dicarbonyl compounds, a one-pot organocatalyzed diastereo- and enantioselective synthesis of polyfunctionalized dihydro- and tetrahydropyran derivatives via a domino Michael-hemiacetalizatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d446259d06cbdc547430be21acd6e46f
https://doi.org/10.1002/chin.201441152
https://doi.org/10.1002/chin.201441152
Publikováno v:
ChemInform. 45
A new highly stereoselective one-pot procedure to synthesize multifunctionalized cyclohexanes is presented which involves an enantioselective Michael addition promoted by low loading of an amino-squaramide catalyst followed by an achiral base catalyz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2840fbeccbfd8a2f43cee0c410c2fe2
https://doi.org/10.1002/chin.201437066
https://doi.org/10.1002/chin.201437066
Publikováno v:
ChemInform. 43
The reaction of β-ketoesters, aromatic nitroalkenes and aromatic α,β-unsaturated aldehydes provides highly substituted cyclohexanes with 6 contiguous stereocenters including a quaternary one.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1981170ed61dd8d354d5429a38ec231
https://doi.org/10.1002/chin.201240058
https://doi.org/10.1002/chin.201240058