Highly stereoselective synthesis of 2, 3-dihydrofurans via a cascade Michael addition-alkylation process: a nitro group as the leaving group. Issue 44 (14th May 2019)
- Record Type:
- Journal Article
- Title:
- Highly stereoselective synthesis of 2, 3-dihydrofurans via a cascade Michael addition-alkylation process: a nitro group as the leaving group. Issue 44 (14th May 2019)
- Main Title:
- Highly stereoselective synthesis of 2, 3-dihydrofurans via a cascade Michael addition-alkylation process: a nitro group as the leaving group
- Authors:
- Mo, Yiran
Liu, Siyang
Liu, Yingying
Ye, Ling
Shi, Zhichuan
Zhao, Zhigang
Li, Xuefeng - Abstract:
- Abstract : The Michael addition-alkylation process proceeded smoothly to provide 2, 3-dihydrofurans as trans -diastereomers in moderate to good isolated yields (33–92%) and excellent enantioselectivities (29–>99% ee). Abstract : The Michael addition-alkylation process between gem -benzoyl-nitrostyrenes and 1, 3-dicarbonyl compounds proceeded smoothly in the presence of a bifunctional squaramide, exclusively providing 2, 3-dihydrofurans as trans -diastereomers in 33–92% isolated yields and excellent enantioselectivities (29–>99% ee).
- Is Part Of:
- Chemical communications. Volume 55:Issue 44(2019)
- Journal:
- Chemical communications
- Issue:
- Volume 55:Issue 44(2019)
- Issue Display:
- Volume 55, Issue 44 (2019)
- Year:
- 2019
- Volume:
- 55
- Issue:
- 44
- Issue Sort Value:
- 2019-0055-0044-0000
- Page Start:
- 6285
- Page End:
- 6288
- Publication Date:
- 2019-05-14
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cc01509d ↗
- 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:
- 10453.xml