ChemInform Abstract: Highly Diastereoselective 1, 6‐Conjugate Addition of Arylboronic Acids to Securinine. Issue 35 (August 2016)
- Record Type:
- Journal Article
- Title:
- ChemInform Abstract: Highly Diastereoselective 1, 6‐Conjugate Addition of Arylboronic Acids to Securinine. Issue 35 (August 2016)
- Main Title:
- ChemInform Abstract: Highly Diastereoselective 1, 6‐Conjugate Addition of Arylboronic Acids to Securinine.
- Authors:
- Perez, Marc
Ayad, Tahar
Maillos, Philippe
Poughon, Valerie
Fahy, Jacques
Ratovelomanana‐Vidal, Virginie - Abstract:
- Abstract: Rhodium catalysis provides access to the single diastereomers of the regioselective C15‐arylation products of securinine in good yields.
- Is Part Of:
- ChemInform. Volume 47:Issue 35(2016)
- Journal:
- ChemInform
- Issue:
- Volume 47:Issue 35(2016)
- Issue Display:
- Volume 47, Issue 35 (2016)
- Year:
- 2016
- Volume:
- 47
- Issue:
- 35
- Issue Sort Value:
- 2016-0047-0035-0000
- Page Start:
- no
- Page End:
- no
- Publication Date:
- 2016-08
- Subjects:
- other bioactive products -- azepine derivatives -- C‐C bond formation -- catalysis, phase‐transfer catalysis -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism)
Chemistry -- Abstracts -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2667 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chin.201635161 ↗
- Languages:
- English
- ISSNs:
- 0931-7597
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3158.195000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2594.xml