ChemInform Abstract: N‐Heterocyclic Carbene—Copper‐Catalyzed Group‐, Site‐, and Enantioselective Allylic Substitution with a Readily Accessible Propargyl(pinacolato)boron Reagent: Utility in Stereoselective Synthesis and Mechanistic Attributes. Issue 2 (23rd December 2015)

Record Type:
Journal Article
Title:
ChemInform Abstract: N‐Heterocyclic Carbene—Copper‐Catalyzed Group‐, Site‐, and Enantioselective Allylic Substitution with a Readily Accessible Propargyl(pinacolato)boron Reagent: Utility in Stereoselective Synthesis and Mechanistic Attributes. Issue 2 (23rd December 2015)
Main Title:
ChemInform Abstract: N‐Heterocyclic Carbene—Copper‐Catalyzed Group‐, Site‐, and Enantioselective Allylic Substitution with a Readily Accessible Propargyl(pinacolato)boron Reagent: Utility in Stereoselective Synthesis and Mechanistic Attributes.
Authors:
Shi, Ying
Jung, Byunghyuck
Torker, Sebastian
Hoveyda, Amir H.
Abstract:
Abstract: The first examples of allylic substitution reaction of allyl diethylphosphates with propargylated (pinacolato)boron compounds (II) are reported to provide generally branched products.
Is Part Of:
ChemInform. Volume 47:Issue 2(2016)
Journal:
ChemInform
Issue:
Volume 47:Issue 2(2016)
Issue Display:
Volume 47, Issue 2 (2016)
Year:
2016
Volume:
47
Issue:
2
Issue Sort Value:
2016-0047-0002-0000
Page Start:
no
Page End:
no
Publication Date:
2015-12-23
Subjects:
diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) -- organo‐silicon compounds -- catalysis, phase‐transfer catalysis
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.201602026 ↗
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:
788.xml