Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel Hugenbusch"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2799-2804 (2018)
Herein we report a reliable method to synthesize mono-functionalized S-diazocines in reproducible yields via intramolecular Baeyer–Mills reactions. Diazocines exhibit excellent photoswitchable properties. As opposed to azobenzenes they are more sta
Externí odkaz:
https://doaj.org/article/bf3554f4fbf7483b8382d2e51c3d26b4
Publikováno v:
Angewandte Chemie. 135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d11f727b0cc6d7aedaa042a6bd5c0f55
https://doi.org/10.1002/ange.202212571
https://doi.org/10.1002/ange.202212571
Publikováno v:
Angewandte Chemie (International ed. in English).
We report on two regioisomeric, diazocine ligands 1 and 2 that can both be photoswitched between the E- and Z-configurations with violet and green light. The self-assembly of the four species (1-Z, 1-E, 2-Z, 2-E) with Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa57a08e402a948aedbb6ad604067dfe
https://pubmed.ncbi.nlm.nih.gov/36215411
https://pubmed.ncbi.nlm.nih.gov/36215411
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2799-2804 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2799-2804 (2018)
Herein we report a reliable method to synthesize mono-functionalized S-diazocines in reproducible yields via intramolecular Baeyer–Mills reactions. Diazocines exhibit excellent photoswitchable properties. As opposed to azobenzenes they are more sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f5f491728d1514a615f2cd8d6fab1f8
http://europepmc.org/articles/PMC6244113
http://europepmc.org/articles/PMC6244113