Supporting Information
| Supporting Information File 1: Experimental. | ||
| Format: PDF | Size: 1.3 MB | Download |
Cite the Following Article
Indenopyrans – synthesis and photoluminescence properties
Andreea Petronela Diac, Ana-Maria Ţepeş, Albert Soran, Ion Grosu, Anamaria Terec, Jean Roncali and Elena Bogdan
Beilstein J. Org. Chem. 2016, 12, 825–834.
https://doi.org/10.3762/bjoc.12.81
How to Cite
Diac, A. P.; Ţepeş, A.-M.; Soran, A.; Grosu, I.; Terec, A.; Roncali, J.; Bogdan, E. Beilstein J. Org. Chem. 2016, 12, 825–834. doi:10.3762/bjoc.12.81
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 901.3 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Worayuthakarn, R.; Suddee, N.; Theppitak, C.; Chainok, K.; Ruchirawat, S.; Thasana, N. Cascade Cyclization of o-(2-Acyl-1-ethynyl)benzaldehydes with Amino Acid Derivatives: Synthesis of Indeno[2,1-c]pyran-3-ones and 1-Oxazolonylisobenzofurans via the Erlenmeyer-Plöchl Azlactone Reaction. ACS omega 2024, 9, 37814–37842. doi:10.1021/acsomega.4c03842
- Piva, O.; Nassar, Y.; Fache, F.; Pelotier, B. Access to Hexahydroindeno[2,1-c]pyran-Based Propellanes by a Domino Prins/Friedel–Crafts Cyclization. Synthesis 2022, 54, 4622–4628. doi:10.1055/a-1882-8128
- Ahuja, M.; Biswas, S.; Sharma, P.; Samanta, S. Synthesis and Photophysical Properties of α‐Pyrone‐fused‐pyrido[3, 2,1‐jk]carbazolone Derivatives : DFT/TD‐DFT Insights. ChemistrySelect 2018, 3, 4354–4360. doi:10.1002/slct.201800369
- Ievlev, M. Y.; Ershov, O. V.; Belikov, M. Y.; Milovidova, A. G.; Tafeenko, V. A.; Nasakin, O. E. Diastereoselective synthesis of 3,4-dihydro-2H-pyran-4-carboxamides through an unusual regiospecific quasi-hydrolysis of a cyano group. Beilstein journal of organic chemistry 2016, 12, 2093–2098. doi:10.3762/bjoc.12.198
