ChemInform Abstract: Diastereoselective Ruthenium Porphyrin‐Catalyzed Tandem Nitrone Formation/1, 3‐Dipolar Cycloaddition for Isoxazolidines. Synthesis, in silico Docking Study and in vitro Biological Activities. Issue 19 (18th April 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: Diastereoselective Ruthenium Porphyrin‐Catalyzed Tandem Nitrone Formation/1, 3‐Dipolar Cycloaddition for Isoxazolidines. Synthesis, in silico Docking Study and in vitro Biological Activities. Issue 19 (18th April 2013)
Main Title:: ChemInform Abstract: Diastereoselective Ruthenium Porphyrin‐Catalyzed Tandem Nitrone Formation/1, 3‐Dipolar Cycloaddition for Isoxazolidines. Synthesis, in silico Docking Study and in vitro Biological Activities.
Authors:: Reddy, Annapureddy Rajasekar
Guo, Zhen
Siu, Fung‐Ming
Lok, Chun‐Nam
Liu, Fuli
Yeung, Kai‐Chung
Zhou, Cong‐Ying
Che, Chi‐Ming
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The described method features a broad scope of alkene compounds, excellent compatibility of various functionalities, neutral reaction conditions, and high regio‐, chemo‐ and diastereoselectivity.</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 19(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 19(2013)
Issue Display:: Volume 44, Issue 19 (2013)
Year:: 2013
Volume:: 44
Issue:: 19
Issue Sort Value:: 2013-0044-0019-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-04-18
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.201319135 ↗
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:: 2977.xml