ChemInform Abstract: Dual Control of the Selectivity in the Formal Nucleophilic Substitution of Bromocyclopropanes en Route to Densely Functionalized, Chirality Rich Cyclopropyl Derivatives. Issue 18 (6th May 2014)

Record Type:: Journal Article
Title:: ChemInform Abstract: Dual Control of the Selectivity in the Formal Nucleophilic Substitution of Bromocyclopropanes en Route to Densely Functionalized, Chirality Rich Cyclopropyl Derivatives. Issue 18 (6th May 2014)
Main Title:: ChemInform Abstract: Dual Control of the Selectivity in the Formal Nucleophilic Substitution of Bromocyclopropanes en Route to Densely Functionalized, Chirality Rich Cyclopropyl Derivatives.
Authors:: Ryabchuk, Pavel
Edwards, Andrew
Gerasimchuk, Nikolay
Rubina, Marina
Rubin, Michael
Abstract:: Abstract: A highly diastereoselective addition of nucleophiles to in situ generated cyclopropenes is successfully accomplished by using a "dual control" strategy.
Is Part Of:: ChemInform. Volume 45:Issue 18(2014)
Journal:: ChemInform
Issue:: Volume 45:Issue 18(2014)
Issue Display:: Volume 45, Issue 18 (2014)
Year:: 2014
Volume:: 45
Issue:: 18
Issue Sort Value:: 2014-0045-0018-0000
Page Start:: no
Page End:: no
Publication Date:: 2014-05-06
Subjects:: cyclopropane derivatives -- cycloalkylphenyl derivatives -- catalysis, phase‐transfer catalysis -- diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- Editor's choice
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.201418059 ↗
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:: 5238.xml