Highly selective domino multicyclizations for forming polycyclic fused acridines and azaheterocyclic skeletons
Organic Letters, ISSN: 1523-7060, Vol: 15, Issue: 7, Page: 1540-1543
2013
- 86Citations
- 17Captures
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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
- Citations86
- Citation Indexes86
- 86
- CrossRef77
- Captures17
- Readers17
- 17
Article Description
Highly selective four-component domino multicyclizations for the synthesis of new fused acridines and azaheterocyclic skeletons have been established by mixing common reactants in isobutyric acid under microwave irradiation. The reactions proceeded at fast rates and were conducted to completion within 20-30 min. Up to seven new chemical bonds, four rings, and four stereocenters were assembled in a convenient one-pot operation. The resulting hexacyclic and pentacyclic fused acridines and their stereochemistry have been fully characterized and determined by X-ray structural analysis. © 2013 American Chemical Society.
Bibliographic Details
American Chemical Society (ACS)
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