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Catalytic Aldehyde and Alcohol Arylation Reactions Facilita..:

Eric S. Isbrandt (6611570) ; Amrah Nasim (7860794) ; Karen Zhao (11384160).
https://figshare.com/articles/journal_contribution/Catalytic_Aldehyde_and_Alcohol_Arylation_Reactions_Facilitated_by_a_1_5-Diaza-3_7-diphosphacyclooctane_Ligand/16569180. , 2021

Link: https://doi.org/10.1021/jacs.1c05661.s001

RT Journal
T1 <Title>Catalytic Aldehyde and Alcohol Arylation Reactions Facilitated by a 1,5-Diaza-3,7-diphosphacyclooctane Ligand</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_16569180&Exemplar=1&LAN=DE
				
A1 Eric S. Isbrandt (6611570)
A1 Amrah Nasim (7860794)
A1 Karen Zhao (11384160)
A1 Stephen G. Newman (1986595)
YR 2021
K1 Biochemistry
K1 Microbiology
K1 Cell Biology
K1 Biotechnology
K1 Immunology
K1 Mental Health
K1 Infectious Diseases
K1 Chemical Sciences not elsewhere classified
K1 insertion step forging
K1 heck type mechanism
K1 diphospha  cyclooctane
K1 access secondary alcohols
K1 2 </ sub
K1 transformation reductive
K1 traditional phosphines
K1 starting materials
K1 related reactions
K1 oxidation state
K1 nickel alkoxide
K1 interrupted carbonyl
K1 enable synthesis
K1 either aldehydes
K1 demonstrating control
K1 catalytic method
K1 catalytic aldehyde
K1 aryl iodides
K1 alcohol reductant
JF https://figshare.com/articles/journal_contribution/Catalytic_Aldehyde_and_Alcohol_Arylation_Reactions_Facilitated_by_a_1_5-Diaza-3_7-diphosphacyclooctane_Ligand/16569180
LK http://dx.doi.org/https://doi.org/10.1021/jacs.1c05661.s001
DO https://doi.org/10.1021/jacs.1c05661.s001
SF ELIB - SuUB Bremen

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