A diastereoselective synthesis of functionalized bis-spirorhodanine-linked cyclopentanes via C(sp3)–H activation. Issue 30 (26th July 2018)
- Record Type:
- Journal Article
- Title:
- A diastereoselective synthesis of functionalized bis-spirorhodanine-linked cyclopentanes via C(sp3)–H activation. Issue 30 (26th July 2018)
- Main Title:
- A diastereoselective synthesis of functionalized bis-spirorhodanine-linked cyclopentanes via C(sp3)–H activation
- Authors:
- Yavari, Issa
Naeimabadi, Maryam
Halvagar, Mohammad R. - Abstract:
- Abstract: A diastereoselective synthesis of bis-spirorhodanine-linked cyclopentane derivatives via the [2 + 2+1] cycloaddition reaction between alkyl ( Z )-2-(3-alkyl-4-oxo-2-thioxothiazolidin-5-ylidene)acetates (alkylidenerhodanines) and azomethine ylides, prepared in situ from iodine mediated reaction of 2-methylquinoline and pyridine in the presence of base, has been developed. The structure of a typical product was confirmed by X-ray crystallography. Graphical abstract:
- Is Part Of:
- Tetrahedron. Volume 74:Issue 30(2018)
- Journal:
- Tetrahedron
- Issue:
- Volume 74:Issue 30(2018)
- Issue Display:
- Volume 74, Issue 30 (2018)
- Year:
- 2018
- Volume:
- 74
- Issue:
- 30
- Issue Sort Value:
- 2018-0074-0030-0000
- Page Start:
- 4145
- Page End:
- 4150
- Publication Date:
- 2018-07-26
- Subjects:
- C(sp3)–H activation -- Azomethine ylide -- Cyclopentanation -- Bis-spirorhodanine-linked cyclopentane -- Iodine
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tet.2018.06.029 ↗
- Languages:
- English
- ISSNs:
- 0040-4020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8796.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 6856.xml