ChemInform Abstract: Highly Enantioselective Synthesis of 2, 3‐Dihydro‐1H‐imidazo[2, 1‐a]isoindol‐5(9bH)‐ones via Catalytic Asymmetric Intramolecular Cascade Imidization—Nucleophilic Addition—Lactamization. Issue 21 (May 2015)

Record Type:
Journal Article
Title:
ChemInform Abstract: Highly Enantioselective Synthesis of 2, 3‐Dihydro‐1H‐imidazo[2, 1‐a]isoindol‐5(9bH)‐ones via Catalytic Asymmetric Intramolecular Cascade Imidization—Nucleophilic Addition—Lactamization. Issue 21 (May 2015)
Main Title:
ChemInform Abstract: Highly Enantioselective Synthesis of 2, 3‐Dihydro‐1H‐imidazo[2, 1‐a]isoindol‐5(9bH)‐ones via Catalytic Asymmetric Intramolecular Cascade Imidization—Nucleophilic Addition—Lactamization.
Authors:
Qiu, Liqin
et al.
Abstract:
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The first efficient preparation of the medicinally relevant title compounds is presented starting from substituted methyl 2‐formylbenzoates.</p> </abstract>
Is Part Of:
ChemInform. Volume 46:Issue 21(2015)
Journal:
ChemInform
Issue:
Volume 46:Issue 21(2015)
Issue Display:
Volume 46, Issue 21 (2015)
Year:
2015
Volume:
46
Issue:
21
Issue Sort Value:
2015-0046-0021-0000
Page Start:
no
Page End:
no
Publication Date:
2015-05
Subjects:
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.201521141 ↗
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:
3528.xml