Nickel-catalyzed aminocarbonylation of aryl halides using carbamoylsilane as an amide source. Issue 71 (21st September 2017)
- Record Type:
- Journal Article
- Title:
- Nickel-catalyzed aminocarbonylation of aryl halides using carbamoylsilane as an amide source. Issue 71 (21st September 2017)
- Main Title:
- Nickel-catalyzed aminocarbonylation of aryl halides using carbamoylsilane as an amide source
- Authors:
- Wen, Xue-Ping
Han, Yu-Ling
Chen, Jian-Xin - Abstract:
- Abstract : The nickel-catalyzed aminocarbonylation reaction of aryl halides using carbamoylsilanes as an amide source in toluene is developed leading to the formation of some tertiary or secondary aryl amides in good yields. Abstract : The nickel-catalyzed aminocarbonylation of aryl halides using carbamoylsilane as an amide source is developed. The procedure can prepare both tertiary and secondary amides, and is applicable to various carbamoylsilanes and aryl halides containing different functional groups. The types and the relative position of substituents on the aryl ring impact the coupling efficiency.
- Is Part Of:
- RSC advances. Volume 7:Issue 71(2017)
- Journal:
- RSC advances
- Issue:
- Volume 7:Issue 71(2017)
- Issue Display:
- Volume 7, Issue 71 (2017)
- Year:
- 2017
- Volume:
- 7
- Issue:
- 71
- Issue Sort Value:
- 2017-0007-0071-0000
- Page Start:
- 45107
- Page End:
- 45112
- Publication Date:
- 2017-09-21
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7ra08009c ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4691.xml