Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kay Merkens"'
Autor:
Irene, Reimche, Haiqian, Yu, Ni Putu, Ariantari, Zhen, Liu, Kay, Merkens, Stella, Rotfuß, Karin, Peter, Ute, Jungwirth, Nadine, Bauer, Friedemann, Kiefer, Jörg-Martin, Neudörfl, Hans-Günther, Schmalz, Peter, Proksch, Nicole, Teusch
Publikováno v:
International journal of molecular sciences. 23(18)
Triple-negative breast cancer (TNBC), representing the most aggressive form of breast cancer with currently no targeted therapy available, is characterized by an inflammatory and hypoxic tumor microenvironment. To date, a broad spectrum of anti-tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bb6f35bdfe867e647b52cfdeb1e2e5f2
https://pubmed.ncbi.nlm.nih.gov/36142230
https://pubmed.ncbi.nlm.nih.gov/36142230
Autor:
Kay Merkens, Adrián Gómez-Suárez
The applications of a-amino ketyl radicals in the synthesis of valuable and potentially biologically-active molecules is currently limited; this is due to the need for strong (Ered > –2 V vs SCE) reductants, such as large excesses of samarium(II) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b2f8fc185a9437f25d160674001ec3
https://doi.org/10.26434/chemrxiv-2022-l6x03
https://doi.org/10.26434/chemrxiv-2022-l6x03
Publikováno v:
Angewandte Chemie. 133:1112-1130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a59bffae07c1c5b52f59eb339a9732f
https://doi.org/10.1002/ange.202010157
https://doi.org/10.1002/ange.202010157
Publikováno v:
Asian Journal of Organic Chemistry. 9:992-1007
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30ef2db6d402595856b49f2a90872f40
https://doi.org/10.1002/ajoc.202000196
https://doi.org/10.1002/ajoc.202000196
Synthesis of Unnatural α‐Amino Acid Derivatives via Light‐Mediated Radical Decarboxylative Processes
Publikováno v:
Advanced Synthesis & Catalysis. 362:2354-2359
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbc9c9957545c1a8a2df45b08e5c5591
https://doi.org/10.1002/adsc.202000300
https://doi.org/10.1002/adsc.202000300
Due to their abundance and readily available synthesis, alcohols provide ideal handles for the selective derivatisation of organic molecules. Radical chemistry offers versatile strategies for the conversion of Csp3–O bonds into a wide range of Csp3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4bc9c75807f8149fa7bbf4166a18790
https://doi.org/10.26434/chemrxiv-2022-w73zr
https://doi.org/10.26434/chemrxiv-2022-w73zr
Autor:
Irene Reimche, Haiqian Yu, Ni Putu Ariantari, Zhen Liu, Kay Merkens, Stella Rotfuß, Karin Peter, Ute Jungwirth, Nadine Bauer, Friedemann Kiefer, Jörg-Martin Neudörfl, Hans-Günther Schmalz, Peter Proksch, Nicole Teusch
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 18; Pages: 10319
Triple-negative breast cancer (TNBC), representing the most aggressive form of breast cancer with currently no targeted therapy available, is characterized by an inflammatory and hypoxic tumor microenvironment. To date, a broad spectrum of anti-tumor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2ddcf8ab9f210548276ddca971cb07
https://doi.org/10.3390/ijms231810319
https://doi.org/10.3390/ijms231810319
Herein we present a highly efficient, light-mediated, deoxygenative protocol to access g-oxo-a-amino acid derivatives.This radical methodology employs photoredox catalysis, in combination with triphenylphosphine, to generate acyl radicals from readil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04f73774e7fa2606ce50cb91d1920435
https://doi.org/10.26434/chemrxiv.13194920.v1
https://doi.org/10.26434/chemrxiv.13194920.v1
Publikováno v:
Chemistry - A European Journal. 24:974-983
Novel E-configured coumarin-based merocyanines were efficiently synthesized by a one-pot, three-component Sonogashira coupling-Michael addition starting from triflyl coumarins, terminal alkynes and secondary amines. The photophysical properties of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deec2a9437aed60b54efde18ec49782e
https://doi.org/10.1002/chem.201704912
https://doi.org/10.1002/chem.201704912