Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Bryan S, Matsuura"'
Publikováno v:
ACS Central Science, Vol 3, Iss 1, Pp 39-46 (2016)
Externí odkaz:
https://doaj.org/article/3550ad4dd9754da3937dbb56d9969b7f
Autor:
David B. Konrad, Klaus-Peter Rühmann, Hiroyasu Ando, Belinda E. Hetzler, Nina Strassner, Kendall N. Houk, Bryan S. Matsuura, Dirk Trauner
Publikováno v:
Science (New York, N.Y.). 377(6604)
Tetrodotoxin (TTX) is a neurotoxic natural product that is an indispensable probe in neuroscience, a biosynthetic and ecological enigma, and a celebrated target of synthetic chemistry. Here, we present a stereoselective synthesis of TTX that proceeds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61b2c2eef394a87dff7d338833be9256
https://pubmed.ncbi.nlm.nih.gov/35862530
https://pubmed.ncbi.nlm.nih.gov/35862530
Autor:
Elizabeth Elacqua, Zhaoxi Zheng, Adri C. T. van Duin, Steven Huss, Shichen Yuan, Bo Chen, Vincent H. Crespi, John V. Badding, Dirk Trauner, Tao Wang, Klaus Schmidt-Rohr, Bryan S. Matsuura
Publikováno v:
Journal of the American Chemical Society. 143:9529-9542
The molecular structure of nanothreads produced by the slow compression of 13C4-furan was studied by advanced solid-state NMR. Spectral editing showed that >95% of carbon atoms were bonded to one hydrogen (C-H) and that there were 2-4% CH2, 0.6% C═
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa50d545fe95665a04b828e8421d10fc
https://doi.org/10.1021/jacs.1c03671
https://doi.org/10.1021/jacs.1c03671
Autor:
Belinda E. Hetzler, David B. Konrad, Peter Ruehmann, Bryan S. Matsuura, Hiroyasu Ando, Dirk Trauner
Tetrodotoxin (TTX) is an indispensable probe in neuroscience, a biosynthetic and ecological enigma, and one of the most celebrated targets of synthetic chemistry. Here, we present a stereoselective synthesis of TTX that proceeds in 22 steps starting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b489ba4b32c8d0413603413bdd97405
https://doi.org/10.33774/chemrxiv-2021-xkftp
https://doi.org/10.33774/chemrxiv-2021-xkftp
Autor:
Julie B. Trads, Katharina Hüll, Bryan S. Matsuura, Laura Laprell, Timm Fehrentz, Nicole Görldt, Krystian A. Kozek, C. David Weaver, Nikolaj Klöcker, David M. Barber, Dirk Trauner
Publikováno v:
Angewandte Chemie. 131:15567-15574
Photopharmacology relies on ligands that change their pharmacodynamics upon photoisomerization. Many of these ligands are azobenzenes that are thermodynamically more stable in their elongated transconfiguration, which predominates in the dark. Often,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e444b486f583b9cb16f433ad78fee4
https://doi.org/10.1002/ange.201905790
https://doi.org/10.1002/ange.201905790
Publikováno v:
Synthesis. 51:2759-2791
The selective modification of α-amino acids and peptides constitutes a pivotal arena for accessing new peptide-based materials and therapeutics. In recent years, visible light photoredox catalysis has appeared as a powerful platform for the activati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec92eea9da0d60f97af4e56ced55a391
https://doi.org/10.1055/s-0037-1611852
https://doi.org/10.1055/s-0037-1611852
Autor:
Bryan S, Matsuura, Steven, Huss, Zhaoxi, Zheng, Shichen, Yuan, Tao, Wang, Bo, Chen, John V, Badding, Dirk, Trauner, Elizabeth, Elacqua, Adri C T, van Duin, Vincent H, Crespi, Klaus, Schmidt-Rohr
Publikováno v:
Journal of the American Chemical Society.
The molecular structure of nanothreads produced by the slow compression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8dbda76fcec2ca64a62b3310245c57d0
https://pubmed.ncbi.nlm.nih.gov/34130458
https://pubmed.ncbi.nlm.nih.gov/34130458
Autor:
Dirk Trauner, Michele Pagano, Marleen Bérouti, Martin Reynders, Bryan S. Matsuura, Daniele Simoneschi, Antonio Marzio
Publikováno v:
Science Advances
We present a modular approach to control the small molecule–mediated degradation of cellular proteins of interest using light.
PROTACs (PROteolysis TArgeting Chimeras) are bifunctional molecules that target proteins for ubiquitylation by an E3
PROTACs (PROteolysis TArgeting Chimeras) are bifunctional molecules that target proteins for ubiquitylation by an E3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::373d99defb9b5ce13e8ad83adf04b269
https://doi.org/10.1126/sciadv.aay5064
https://doi.org/10.1126/sciadv.aay5064
Autor:
Martin Reynders, Tongil Ko, Katharina Hüll, Martin S. Maier, Bryan S. Matsuura, Dirk Trauner, Philipp Leippe, Lukas Schäffer
Publikováno v:
Journal of the American Chemical Society
Azobenzenes are versatile photoswitches that have found widespread use in a variety of fields, ranging from photo-pharmacology to the material sciences. In addition to regular azobenzenes the cyclic diazocines have recently emerged. Although diazocin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06b642c1763033b0fd979a6dc2e00ffb
https://pubmed.ncbi.nlm.nih.gov/31584272
https://pubmed.ncbi.nlm.nih.gov/31584272
Publikováno v:
ACS Central Science
ACS Central Science, Vol 3, Iss 1, Pp 39-46 (2016)
ACS Central Science, Vol 3, Iss 1, Pp 39-46 (2016)
Aplydactone (1) is a brominated ladderane sesquiterpenoid that was isolated from the sea hare Aplysia dactylomela together with the chamigranes dactylone (2) and 10-epi-dactylone (3). Given the habitat of A. dactylomela, it seems likely that 1 is for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79e2534b092d7b0a22b33bd4256fd96f
https://doi.org/10.1021/acscentsci.6b00293
https://doi.org/10.1021/acscentsci.6b00293