ChemInform Abstract: Reaction of 5‐Aryloxazolidines with Arylmagnesium Bromides as a New Route to N‐Benzyl‐β‐hydroxyphenethylamines as Starting Materials for the Preparation of 4‐Aryl‐1, 2, 3, 4‐tetrahydroisoquinolines. Issue 36 (15th August 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: Reaction of 5‐Aryloxazolidines with Arylmagnesium Bromides as a New Route to N‐Benzyl‐β‐hydroxyphenethylamines as Starting Materials for the Preparation of 4‐Aryl‐1, 2, 3, 4‐tetrahydroisoquinolines. Issue 36 (15th August 2013)
Main Title:: ChemInform Abstract: Reaction of 5‐Aryloxazolidines with Arylmagnesium Bromides as a New Route to N‐Benzyl‐β‐hydroxyphenethylamines as Starting Materials for the Preparation of 4‐Aryl‐1, 2, 3, 4‐tetrahydroisoquinolines.
Authors:: Moshkin, Vladimir S.
Sosnovskikh, Vyacheslav Ya.
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The two‐step sequence involves ring‐opening of 5‐aryloxazolidines in the presence of arylmagnesium bromides followed by acid‐catalyzed cyclization of the resulting amino alcohols.</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 36(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 36(2013)
Issue Display:: Volume 44, Issue 36 (2013)
Year:: 2013
Volume:: 44
Issue:: 36
Issue Sort Value:: 2013-0044-0036-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-08-15
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.201336147 ↗
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:: 3606.xml