ChemInform Abstract: Electrophilic Addition of Allylic Carbocations to 2‐Cyclopropylidene‐2‐arylethanols: A Strategy to 3‐Oxabicyclo[3.2.0]heptanes. Issue 15 (15th April 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: Electrophilic Addition of Allylic Carbocations to 2‐Cyclopropylidene‐2‐arylethanols: A Strategy to 3‐Oxabicyclo[3.2.0]heptanes. Issue 15 (15th April 2014)
Main Title:: ChemInform Abstract: Electrophilic Addition of Allylic Carbocations to 2‐Cyclopropylidene‐2‐arylethanols: A Strategy to 3‐Oxabicyclo[3.2.0]heptanes.
Authors:: Meng, Bo
Huang, Xian
Wu, Luling
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>The construction of 3‐oxabicyclo[3.2.0]heptanes is developed using the electrophilic addition of carbocations generated from functionalized allylic alcohols to cyclopropylidene substituted ethanols (I).</p> </abstract>
Is Part Of:: ChemInform. Volume 45:Issue 15(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 15(2014)
Issue Display:: Volume 45, Issue 15 (2014)
Year:: 2014
Volume:: 45
Issue:: 15
Issue Sort Value:: 2014-0045-0015-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-04-15
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.201415114 ↗
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:: 4292.xml