ChemInform Abstract: Highly Enantioselective Synthesis of 1, 2, 3‐Substituted Cyclopropanes by Using α‐Iodo‐ and α‐Chloromethylzinc Carbenoids. Issue 14 (20th March 2013)

Record Type:: Journal Article
Title:: ChemInform Abstract: Highly Enantioselective Synthesis of 1, 2, 3‐Substituted Cyclopropanes by Using α‐Iodo‐ and α‐Chloromethylzinc Carbenoids. Issue 14 (20th March 2013)
Main Title:: ChemInform Abstract: Highly Enantioselective Synthesis of 1, 2, 3‐Substituted Cyclopropanes by Using α‐Iodo‐ and α‐Chloromethylzinc Carbenoids.
Authors:: Beaulieu, Louis‐Philippe B.
Zimmer, Lucie E.
Gagnon, Alexandre
Charette, Andre B.
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Trans‐iodocyclopropylmethanols obtained with excellent enantioselectivities by the presented new asymmetric iodocyclopropanation are further converted into 1, 2, 3‐substituted cyclopropanes either by reaction with electrophiles (X) or Negishi coupling with aryl iodides (XII).</p> </abstract>
Is Part Of:: ChemInform. Volume 44:Issue 14(2013)
Journal:: ChemInform
Issue:: Volume 44:Issue 14(2013)
Issue Display:: Volume 44, Issue 14 (2013)
Year:: 2013
Volume:: 44
Issue:: 14
Issue Sort Value:: 2013-0044-0014-0000
Page Start:: no
Page End:: no
Publication Date:: 2013-03-20
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.201314056 ↗
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:: 3964.xml