Conversion of 4,4-difluoro-4-bora-3a, 4a-diaza-s-indacenes (F-BODIPYs) to dipyrrins with a microwave-promoted deprotection strategy
Organic Letters, ISSN: 1523-7060, Vol: 12, Issue: 7, Page: 1424-1427
2010
- 53Citations
- 42Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations53
- Citation Indexes53
- 53
- CrossRef52
- Captures42
- Readers42
- 42
- Mentions1
- News Mentions1
- News1
Most Recent News
Microwave-assisted reduction of F-BODIPYs and dipyrrins to generate dipyrromethanes
Introduction Dipyrrins present a useful ligand scaffold, with significant interest being devoted to dipyrrinato complexes of transition metals and boron. (1,2) There are limited reports
Article Description
"Chemical eqation presented" 4,4-Difluoro-4-bora-3a,4a-diaza-s- indacenes (F-BODIPYs) have been deprotected to give the corresponding free-base dipyrrins by heating a solution of the F-BODIPY in tert-butanol under 600 W of microwave irradiation in the presence of 6 equiv of potassium tert-butoxide for 40 min at 92 C. Investigations of BODIPY modification at the meso position have also been undertaken and a meso-butyl product has been isolated. © 2010 American Chemical Society.
Bibliographic Details
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