(+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane. Issue 1 (18th November 2016)
- Record Type:
- Journal Article
- Title:
- (+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane. Issue 1 (18th November 2016)
- Main Title:
- (+)-Camphor-mediated kinetic resolution of allylalanes: a strategy towards enantio-enriched cyclohex-2-en-1-ylalane
- Authors:
- Coffinet, Michaël
Massicot, Fabien
Joseph, Jomy
Behr, Jean-Bernard
Jaroschik, Florian
Vasse, Jean-Luc - Abstract:
- Abstract : The (+)-camphor-mediated kinetic resolution of cyclohex-2-en-1-ylalane is presented. Abstract : An efficient (+)-camphor-mediated kinetic resolution of racemic cyclohex-2-en-1-ylalane is described. This approach provides an enantiomerically enriched form of the alane, in situ available for synthetic uses. Applied to the allylation of aldehydes, this protocol leads to the corresponding homoallylalcohols in a highly enantioselective manner.
- Is Part Of:
- Chemical communications. Volume 53:Issue 1(2017)
- Journal:
- Chemical communications
- Issue:
- Volume 53:Issue 1(2017)
- Issue Display:
- Volume 53, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 53
- Issue:
- 1
- Issue Sort Value:
- 2016-0053-0001-0000
- Page Start:
- 111
- Page End:
- 114
- Publication Date:
- 2016-11-18
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6cc08649g ↗
- Languages:
- English
- ISSNs:
- 1359-7345
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3139.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2417.xml