ChemInform Abstract: Chiral Lewis Base‐Catalyzed, Enantioselective Reduction of Unprotected β‐Enamino Esters with Trichlorosilane. Issue 32 (July 2016)
- Record Type:
- Journal Article
- Title:
- ChemInform Abstract: Chiral Lewis Base‐Catalyzed, Enantioselective Reduction of Unprotected β‐Enamino Esters with Trichlorosilane. Issue 32 (July 2016)
- Main Title:
- ChemInform Abstract: Chiral Lewis Base‐Catalyzed, Enantioselective Reduction of Unprotected β‐Enamino Esters with Trichlorosilane.
- Authors:
- Ye, Jianheng
Wang, Chao
Chen, Lin
Wu, Xinjun
Zhou, Li
Sun, Jian - Abstract:
- Abstract: Conditions for the reduction of β‐aryl substituted enamino esters are developed which provide chiral β‐aryl‐β‐amino esters in high yields and with very high enantiomeric excesses.
- Is Part Of:
- ChemInform. Volume 47:Issue 32(2016)
- Journal:
- ChemInform
- Issue:
- Volume 47:Issue 32(2016)
- Issue Display:
- Volume 47, Issue 32 (2016)
- Year:
- 2016
- Volume:
- 47
- Issue:
- 32
- Issue Sort Value:
- 2016-0047-0032-0000
- Page Start:
- no
- Page End:
- no
- Publication Date:
- 2016-07
- Subjects:
- aminocarboxylic acids (hydrazinocarboxylic acids) and esters (benzene compounds) -- aminocarboxylic acids (hydrazinocarboxylic acids) and esters (acyclic compounds) -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- organocatalysis
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.201632078 ↗
- 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:
- 14966.xml