Regio- and stereoselective syntheses of allylic thioethers under metal free conditions
RSC Advances, ISSN: 2046-2069, Vol: 7, Issue: 49, Page: 30594-30602
2017
- 19Citations
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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
- Citations19
- Citation Indexes19
- 19
- CrossRef18
Article Description
A metal free, regio and stereoselective syntheses of allylic thioethers using allyl iodides and aryl or alkyl disulfides as coupling partners is described. The densely functionalized allyl iodides having different stereochemistry (E & Z) reacted well with a variety of disulfides in a regio and stereoselective manner providing the resulting allyl aryl thioethers in 62-92% yields.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85021646005&origin=inward; http://dx.doi.org/10.1039/c7ra04817c; https://xlink.rsc.org/?DOI=C7RA04817C; http://xlink.rsc.org/?DOI=C7RA04817C; http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA04817C; https://dx.doi.org/10.1039/c7ra04817c; https://pubs.rsc.org/en/content/articlelanding/2017/ra/c7ra04817c
Royal Society of Chemistry (RSC)
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