Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Dennis, Svatunek"'
Publikováno v:
ACS Omega, Vol 9, Iss 44, Pp 44224-44232 (2024)
Externí odkaz:
https://doaj.org/article/39f64061d67f45d5854da9e41f325c00
Publikováno v:
Accounts of Chemical Research. 55:2467-2479
ConspectusThis Account describes our quest to understand and predict organic reactivity, a principal goal of physical and theoretical organic chemistry. The focus is on the development and testing of models for the prediction of cycloaddition reactiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b38fa6c2fb9d136259a0adf7bad1f25
https://doi.org/10.1021/acs.accounts.2c00343
https://doi.org/10.1021/acs.accounts.2c00343
Publikováno v:
Journal of the American Chemical Society, vol 144, iss 24
1,2,3-Triazines and 1,2,3,5-tetrazines react rapidly, efficiently, and selectively with amidines to form pyrimidines/1,3,5-triazines, exhibiting an orthogonal reactivity with 1,2,4,5-tetrazine-based conjugation chemistry. Whereas the mechanism of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a799dd50f55614ff89028fdbbb441f50
https://doi.org/10.1021/jacs.2c03726
https://doi.org/10.1021/jacs.2c03726
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f454bdbdc6d3f0f9745cffd5ca1614a3
https://doi.org/10.1002/chem.202301169
https://doi.org/10.1002/chem.202301169
Publikováno v:
Chemistry – A European Journal. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::387e6cc6ca7ede0a882661b36028019e
https://doi.org/10.1002/chem.202300345
https://doi.org/10.1002/chem.202300345
Publikováno v:
Monatshefte für Chemie - Chemical Monthly.
The concise synthesis of a potentially “super-armed” glucuronidation donor is reported. The α-anomer was crystallized and analyzed by single crystal X-ray diffraction. The pyranose ring was found to be in a twist-boat conformation in the solid s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fff8bc91a3b6743c4d56892a6d4c4268
https://doi.org/10.1007/s00706-022-03009-4
https://doi.org/10.1007/s00706-022-03009-4
Autor:
Walter Kuba, Barbara Sohr, Patrick Keppel, Dennis Svatunek, Viktoria Humhal, Berthold Stöger, Marion Goldeck, Jonathan C. T. Carlson, Hannes Mikula
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany).
Modified trans-cyclooctenes (TCO) are capable of highly efficient molecular manipulations in biological environments, driven by the bioorthogonal reaction with tetrazines (Tz). The development of click-cleavable TCO has fueled the field of in vivo ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e8e4d104fa341200d06cc140f67cdae
https://pubmed.ncbi.nlm.nih.gov/36250260
https://pubmed.ncbi.nlm.nih.gov/36250260
Autor:
Hannes Mikula, Julia Weber, Dennis Svatunek, Philipp Skrinjar, Gerhard Adam, Rudolf Krska, Christian Hametner, Johannes Fröhlich
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1129-1134 (2014)
The development of a reliable procedure for the synthesis of the 16-glucoside and 16-sulfate of the resorcylic acid lactone (RAL) type compound zearalenone is presented. Different protective group strategies were considered and applied to enable the
Externí odkaz:
https://doaj.org/article/e22719284d264779af3f611b623eccde
Publikováno v:
Angew Chem Int Ed Engl
Strained cyclic allenes, first discovered in 1966 by Wittig and coworkers, have recently emerged as valuable synthetic building blocks. Previous experimental investigations, and computations reported here, demonstrate that the Diels–Alder reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ba213354ecb1c91f84ec8f623ff06b9
https://doi.org/10.1002/ange.202101809
https://doi.org/10.1002/ange.202101809
How the Lewis Base F-Catalyzes the 1,3-Dipolar Cycloaddition between Carbon Dioxide and Nitrilimines
Publikováno v:
The Journal of organic chemistry, vol 86, iss 5
Journal of Organic Chemistry, 86(5), 4320–4325. American Chemical Society ({ACS})
Svatunek, D, Hansen, T, Houk, K N & Hamlin, T A 2021, ' How the Lewis Base F-Catalyzes the 1,3-Dipolar Cycloaddition between Carbon Dioxide and Nitrilimines ', The Journal of organic chemistry, vol. 86, no. 5, pp. 4320-4325 . https://doi.org/10.1021/acs.joc.0c02963
The Journal of organic chemistry, 86(5), 4320-4325. American Chemical Society
The Journal of Organic Chemistry
Journal of Organic Chemistry, 86(5), 4320–4325. American Chemical Society ({ACS})
Svatunek, D, Hansen, T, Houk, K N & Hamlin, T A 2021, ' How the Lewis Base F-Catalyzes the 1,3-Dipolar Cycloaddition between Carbon Dioxide and Nitrilimines ', The Journal of organic chemistry, vol. 86, no. 5, pp. 4320-4325 . https://doi.org/10.1021/acs.joc.0c02963
The Journal of organic chemistry, 86(5), 4320-4325. American Chemical Society
The Journal of Organic Chemistry
The mechanism of the Lewis base F- catalyzed 1,3-dipolar cycloaddition between CO2 and nitrilimines is interrogated using DFT calculations. F- activates the nitrilimine, not CO2 as proposed in the literature, and imparts a significant rate enhancemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7369989e1400491ddc8fdc06431b3481
http://www.scopus.com/inward/record.url?scp=85101663148&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85101663148&partnerID=8YFLogxK