DMAP-catalyzed Diels–Alder reaction of 3-hydroxy-2-pyrone and methyleneindolinones for the synthesis of spirocyclic oxindoles. Issue 23 (10th June 2015)
- Record Type:
- Journal Article
- Title:
- DMAP-catalyzed Diels–Alder reaction of 3-hydroxy-2-pyrone and methyleneindolinones for the synthesis of spirocyclic oxindoles. Issue 23 (10th June 2015)
- Main Title:
- DMAP-catalyzed Diels–Alder reaction of 3-hydroxy-2-pyrone and methyleneindolinones for the synthesis of spirocyclic oxindoles
- Authors:
- Zhou, Ming-Qiang
Zhao, Jian-Qiang
You, Yong
Xu, Xiao-Ying
Zhang, Xiao-Mei
Yuan, Wei-Cheng - Abstract:
- Abstract: An efficient Diels–Alder reaction of 3-hydroxy-2-pyrone with a wide range of methyleneindolinones has been developed by employing 4-dimethylaminopyridine as a catalyst under mild reaction conditions. This process provides a promising method for the construction of structurally diverse spirocyclic oxindoles containing bicyclic lactone motif with moderate diastereoselectivities and good to excellent yields. Graphical abstract:
- Is Part Of:
- Tetrahedron. Volume 71:Issue 23(2015)
- Journal:
- Tetrahedron
- Issue:
- Volume 71:Issue 23(2015)
- Issue Display:
- Volume 71, Issue 23 (2015)
- Year:
- 2015
- Volume:
- 71
- Issue:
- 23
- Issue Sort Value:
- 2015-0071-0023-0000
- Page Start:
- 3903
- Page End:
- 3908
- Publication Date:
- 2015-06-10
- Subjects:
- Diels–Alder reaction -- 3-Hydroxy-2-pyrone -- Methyleneindolinones -- Spirocyclic oxindoles -- 4-Dimethylaminopyridine
Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.tet.2015.04.032 ↗
- 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:
- 7355.xml