ChemInform Abstract: Nickel‐Catalyzed Suzuki—Miyaura Coupling of a Tertiary Iodocyclopropane with Wide Boronic Acid Substrate Scope: Coupling Reaction Outcome Depends on Radical Species Stability. Issue 30 (July 2015)

Record Type:: Journal Article
Title:: ChemInform Abstract: Nickel‐Catalyzed Suzuki—Miyaura Coupling of a Tertiary Iodocyclopropane with Wide Boronic Acid Substrate Scope: Coupling Reaction Outcome Depends on Radical Species Stability. Issue 30 (July 2015)
Main Title:: ChemInform Abstract: Nickel‐Catalyzed Suzuki—Miyaura Coupling of a Tertiary Iodocyclopropane with Wide Boronic Acid Substrate Scope: Coupling Reaction Outcome Depends on Radical Species Stability.
Authors:: Yotsuji, Keisuke
Hoshiya, Naoyuki
Kobayashi, Takaaki
Fukuda, Hayato
Abe, Hiroshi
Arisawa, Mitsuhiro
Shuto, Satoshi
Abstract:: <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>This is the first transition metal‐catalyzed Suzuki—Miyaura coupling reaction between a tertiary alkyl halide and a wide variety of aromatic boronic acids.</p> </abstract>
Is Part Of:: ChemInform. Volume 46:Issue 30(2015)
Journal:: ChemInform
Issue:: Volume 46:Issue 30(2015)
Issue Display:: Volume 46, Issue 30 (2015)
Year:: 2015
Volume:: 46
Issue:: 30
Issue Sort Value:: 2015-0046-0030-0000
Page Start:: no
Page End:: no
Publication Date:: 2015-07
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.201530086 ↗
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:: 3241.xml