Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alissa C Götzinger"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 2024-2077 (2024)
Pyrazoles are rarely found in nature but are traditionally used in the agrochemical and pharmaceutical industries, while other areas of use are also actively developing. However, they have also found numerous other applications. The search for new an
Externí odkaz:
https://doaj.org/article/c4c8dfdcb1e64ce09a7f54cae8329d37
Publikováno v:
Journal of the American Chemical Society. 142:19819-19824
Chiral cyclooctadienes are a frequently occurring scaffold in natural products and specialty chemicals, and are used as ligands in asymmetric catalysis. Accessing substituted cyclooctadienes in an efficient asymmetric fashion has been notoriously cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::122226a998f9e3feebc9e0989ef5a8b5
https://doi.org/10.1021/jacs.0c09486
https://doi.org/10.1021/jacs.0c09486
Autor:
Alissa C. Götzinger, Bettina Wüstenberg, Werner Bonrath, Jonathan Medlock, Marc-André Müller, Thomas Netscher, René T. Stemmler
Publikováno v:
Free Radical Biology and Medicine. 189:26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34e1ce56cf8a83cb68e836f3c2f550f6
https://doi.org/10.1016/j.freeradbiomed.2022.06.118
https://doi.org/10.1016/j.freeradbiomed.2022.06.118
Publikováno v:
ChemistrySelect. 3:5216-5219
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c59c750b15ff2162b9198eeeaa25fc1d
https://doi.org/10.1002/slct.201801233
https://doi.org/10.1002/slct.201801233
3-Phenothiazinyl propiolates – Fluorescent electrophores by Sonogashira coupling of ethyl propiolate
Publikováno v:
Dyes and Pigments. 143:308-316
Fluorescent ethyl 3-phenothiazinyl propiolates with reversible Nernstian oxidation potentials were efficiently synthesized by an improved Sonogashira coupling of aryl iodides and ethyl propiolate. The versatility of this modified alkynylation was ill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb91ab8df15571da5265c753d2cd3884
https://doi.org/10.1016/j.dyepig.2017.04.049
https://doi.org/10.1016/j.dyepig.2017.04.049
Autor:
Julian Rechmann, Alissa C. Götzinger, Adnan Sarfraz, Elena Dirksen, Thomas Müller, Andreas Erbe
Publikováno v:
Langmuir. 31:7306-7316
Phenothiazines are redox-active, fluorescent molecules with potential applications in molecular electronics. Phosphonated phenylethynyl phenothiazine can be easily obtained in a four-step synthesis, yielding a molecule with a headgroup permitting sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8771d56a62f6013742306585adc68d7d
https://doi.org/10.1021/acs.langmuir.5b01370
https://doi.org/10.1021/acs.langmuir.5b01370
Publikováno v:
The Journal of organic chemistry. 81(21)
Consecutive four-component coupling–coupling–cyclocondensation syntheses of pyrazoles and pyrimidines were developed by taking advantage of the provisional, sequentially Pd-catalyzed one-pot generation of alkynones from aryl iodides, ethynylmagne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30da3ee2d54d22f4508a561ce52606b0
https://pubmed.ncbi.nlm.nih.gov/27403574
https://pubmed.ncbi.nlm.nih.gov/27403574
Autor:
Thomas Müller, Alissa C. Götzinger
Publikováno v:
Organicbiomolecular chemistry. 14(14)
Alkynones as well as unsymmetrically substituted tolanes (diarylalkynes) can be rapidly generated in a one-pot fashion via sequential palladium catalysis. Terminal alkynes, formed in situ by protecting-group free palladium-catalyzed coupling of aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f2c44b16594a7f0412f1c557a7ebc50
https://pubmed.ncbi.nlm.nih.gov/26988334
https://pubmed.ncbi.nlm.nih.gov/26988334