izpis_h1_title_alt

Photocatalyst-free wavelength-dependant sequential ring transformations of pyrazolo[1,2-a]pyrazolones
ID Kulašić, Ines (Author), ID Petek, Nejc (Author), ID Brodnik, Helena (Author), ID Grošelj, Uroš (Author), ID Svete, Jurij (Author), ID Štefane, Bogdan (Author)

.pdfPDF - Presentation file, Download (3,29 MB)
MD5: 86C219D3F83CCC3E8E7391625DAB167C
URLURL - Source URL, Visit https://onlinelibrary.wiley.com/doi/10.1002/adsc.202400684 This link opens in a new window

Abstract
We report sequential wavelength-selective photochemical transformations of 1-alkenylpyrazolo[1,2-a]pyrazolones to pyrazolo[1,2-a][1,2]diazepines or cyclobuta[c]pyrazolo[1,2-a]pyrazolones. Irradiation of 1-alkenylpyrazolo[1,2-a]pyrazolones with visible-light (blue LED, 457 nm) induced selective ‘ring switching’ transformation into pyrazolo[1,2-a][1,2]diazepines, which underwent electrocyclisation yielding cyclobuta[c]pyrazolo[1,2-a]pyrazolones upon irradiation with UV A light (black LED, 365 nm). Due to the very narrow irradiation wavelength now available from OLED sources, the selective formation of either 5,7-bicyclic or 5,5,4-tricyclic ring systems from the 5,5-bicyclic starting material is possible by changing the wavelength of the irradiation source. The transformations took place under mild conditions in the absence of additives or photocatalysts. Mechanistic studies indicate that these transformations proceed through the formation of an excited triplet state of the substrate, followed by selective homolytic C(1) N(8) bond cleavage, intersystem crossing, and cyclization of the zwitterionic intermediate on the ground potential energy surface. The subsequent photoinduced disrotatory stereospecific 4π-electrocyclization of the 5,7-bicyclic systems leads to 3D-rich 5,5,4-tricyclic products.

Language:English
Keywords:C-N bond cleavage, heterocycles, visible-light, ring transformation, photocatalyst-free transformations
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2024
Number of pages:Str. 4441-4451
Numbering:Vol. 366, iss. 21
PID:20.500.12556/RUL-165184 This link opens in a new window
UDC:547.77:544.52
ISSN on article:1615-4169
DOI:10.1002/adsc.202400684 This link opens in a new window
COBISS.SI-ID:209299715 This link opens in a new window
Publication date in RUL:26.11.2024
Views:43
Downloads:187
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Advanced synthesis & catalysis
Publisher:Wiley
ISSN:1615-4169
COBISS.SI-ID:22996997 This link opens in a new window

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.

Secondary language

Language:Slovenian
Keywords:cepitev C-N vezi, heterocikli, vidna svetloba, pretvorbe obročev, pretvorbe brez katalizatorja

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0179
Name:Napredna organska sinteza in kataliza

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back