Enantioselective synthesis of spirooxindole benzoquinolizines via organo-catalyzed cascade reactions
Organic and Biomolecular Chemistry, ISSN: 1477-0520, Vol: 15, Issue: 4, Page: 778-781
2017
- 21Citations
- 7Captures
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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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations21
- Citation Indexes21
- 21
- CrossRef19
- Captures7
- Readers7
Article Description
A Michael-Mannich-hemiaminalization-dehydration cascade reaction was developed for the construction of spirooxindole benzoquinolizine derivatives. Additionally, spirooxindole benzoindolizidine was prepared conveniently through a ring-contracted rearrangement reaction from spirooxindole benzoquinolizine.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85010661887&origin=inward; http://dx.doi.org/10.1039/c6ob02157c; http://www.ncbi.nlm.nih.gov/pubmed/27808321; http://xlink.rsc.org/?DOI=C6OB02157C; http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02157C; https://xlink.rsc.org/?DOI=C6OB02157C; https://dx.doi.org/10.1039/c6ob02157c; https://pubs.rsc.org/en/content/articlelanding/2017/ob/c6ob02157c
Royal Society of Chemistry (RSC)
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