530116-20-2Relevant articles and documents
An efficient: T -BuOK promoted C3-chalcogenylation of indoles with dichalcogenides
Yu, Yuanzu,Zhou, Yan,Song, Zengqiang,Liang, Guang
, p. 4958 - 4962 (2018)
A versatile and efficient method for the synthesis of 3-chalcogenyl-indoles from indoles and dichalcogenides employing t-BuOK as a promoter at room temperature has been achieved. The present protocol exhibited a broad functional group tolerance. Diverse 3-sulfenyl- and 3-selenyl-indoles were rapidly obtained in good to excellent yields with high regioselectivities. It is noteworthy that this transformation was applicable to N-protected and N-unprotected indoles, allowing N-deprotection and C3-chalcogenylation of indoles in one step.
CANNABINOID RECEPTOR LIGANDS
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Page/Page column 73-74, (2008/06/13)
Compounds of Formula (I) and/or pharmaceutically acceptable salts, solvates or prodrugs thereof, or pharmaceutical compositions containing such compounds exhibit anti-inflammatory and immunomodulatory activity, and can be effective asCB2 receptor ligands in treating cancer and inflammatory, immunomodulatory or respiratory diseases or conditions.