Synthesis of aryl acetamides by aminocarbonylation of benzylic chlorides using carbamoylsilane as an amide source. Issue 7 (3rd April 2017)
- Record Type:
- Journal Article
- Title:
- Synthesis of aryl acetamides by aminocarbonylation of benzylic chlorides using carbamoylsilane as an amide source. Issue 7 (3rd April 2017)
- Main Title:
- Synthesis of aryl acetamides by aminocarbonylation of benzylic chlorides using carbamoylsilane as an amide source
- Authors:
- Zhang, Wenjun
Han, Shenghua
Chen, Jianxin - Abstract:
- ABSTRACT: Using N -methyl- N -(1-phenyl)ethylcarbamoyl(trimethyl)silane as an amide source, the direct transformation of benzylic chlorides into the corresponding aryl acetamides through palladium-catalyzed aminocarbonylation is described. The electronic property and the relative position of substituents on the aromatic ring impact the coupling efficiency. GRAPHICAL ABSTRACT:
- Is Part Of:
- Synthetic communications. Volume 47:Issue 7(2017)
- Journal:
- Synthetic communications
- Issue:
- Volume 47:Issue 7(2017)
- Issue Display:
- Volume 47, Issue 7 (2017)
- Year:
- 2017
- Volume:
- 47
- Issue:
- 7
- Issue Sort Value:
- 2017-0047-0007-0000
- Page Start:
- 704
- Page End:
- 709
- Publication Date:
- 2017-04-03
- Subjects:
- Amides -- aminocarbonylation -- benzylic halides -- carbamoylsilane -- synthetic methods
Organic compounds -- Synthesis -- Periodicals
Chemistry, Organic
Synthesis
547.205 - Journal URLs:
- http://www.tandfonline.com/toc/lsyc20/current ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/00397911.2017.1281958 ↗
- Languages:
- English
- ISSNs:
- 0039-7911
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8586.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 431.xml