NDLI: Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert-butyl isocyanide insertion.

Content Provider	Semantic Scholar
Author	Duan, Huaqing Chen, Zhong Ning Han, Li Feng, Yulin Zhu, Yongming Yang, Shilin
Copyright Year	2015
Abstract	A simple and efficient strategy for the synthesis of indane-1,3-dione derivatives through a palladium(0)-catalyzed reaction incorporating tert-butyl isocyanide has been developed. In addition, by applying this protocol as the key step, indenopyrazole derivatives can be easily synthesized in high yields in a one-pot procedure. This methodology is tolerant of a wide range of substrates and applicable to library synthesis.
Starting Page	477
Ending Page	479
Page Count	3
File Format	PDF HTM / HTML
Alternate Webpage(s)	http://www.rsc.org/suppdata/c5/ob/c5ob00472a/c5ob00472a1.pdf
Alternate Webpage(s)	http://pubs.rsc.org/en/content/getauthorversionpdf/C5OB00472A
PubMed reference number	26007325v1
Alternate Webpage(s)	https://doi.org/10.1039/c5ob00472a
DOI	10.1039/c5ob00472a
Journal	Organic & biomolecular chemistry
Volume Number	13
Issue Number	24
Language	English
Access Restriction	Open
Subject Keyword	Clinical act of insertion Insertion Mutation Marijuana Abuse Methyl tert-butyl ether:MCnc:Pt:Bld:Qn Palladium
Content Type	Text
Resource Type	Article

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Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert-butyl isocyanide insertion.