Solid-state and solvent-free synthesis of azines, pyrazoles, and pyridazinones using solid hydrazine
Tetrahedron Letters, ISSN: 0040-4039, Vol: 54, Issue: 11, Page: 1384-1388
2013
- 51Citations
- 28Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Article Description
Azines, pyrazoles, and pyridazinones were isolated as the sole products in high yields (>97%) by grinding solid hydrazine (H 3 N + NHCO 2 − ) with di-carbonyl compounds or by their reaction in the absence of solvent. Neither catalysts nor additives were needed to promote the reactions. The solid-state and solvent-free reactions proceeded under ambient conditions and did not produce any wastes other than water and carbon dioxide. They are operationally easy, environmentally safe, and readily scalable, allowing for highly selective synthesis of compounds containing the hydrazine motif.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0040403912022599; http://dx.doi.org/10.1016/j.tetlet.2012.12.106; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84874937196&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0040403912022599; https://dx.doi.org/10.1016/j.tetlet.2012.12.106
Elsevier BV
Provide Feedback
Have ideas for a new metric? Would you like to see something else here?Let us know