Armando Carlone

Prof. Armando Carlone

Department of Physical and Chemical Sciences, Università degli Studi dell'Aquila, via Vetoio, 67100 L'Aquila, Italy
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 July 2008 in Angewandte Chemie International Edition
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Journal Article
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PMPaolo Melchiorre
Paolo Melchiorre
MMMauro Marigo
Mauro Marigo
Armando CarloneArmando Carlone
Armando Carlone
GBGiuseppe Bartoli
Giuseppe Bartoli

8 June 2016 in Nature
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Journal Article
Closed access
MWMiriam R. Wilson
Miriam R. Wilson
JSJordi Solà
Jordi Solà
Armando CarloneArmando Carlone
Armando Carlone
SGStephen Goldup
Stephen Goldup
NLNathalie Lebrasseur
Nathalie Lebrasseur
DLDavid A. Leigh
David A. Leigh

1 March 2007 in Organic Letters
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Journal Article
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GBGiuseppe Bartoli
Giuseppe Bartoli
MBMarcella Bosco
Marcella Bosco
Armando CarloneArmando Carlone
Armando Carlone
FPFabio Pesciaioli
Fabio Pesciaioli
LSLetizia Sambri
Letizia Sambri
PMPaolo Melchiorre
Paolo Melchiorre

13 April 2012 in Angewandte Chemie International Edition
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Journal Article
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VBVictor Blanco
Victor Blanco
Armando CarloneArmando Carlone
Armando Carlone
KHKevin D. Hänni
Kevin D. Hänni
DLDavid A. Leigh
David A. Leigh
BLBartosz Lewandowski
Bartosz Lewandowski

29 January 2007 in Angewandte Chemie International Edition
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Journal Article
Closed access
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Armando CarloneArmando Carlone
Armando Carlone
SCSilvia Cabrera
Silvia Cabrera
MMMauro Marigo
Mauro Marigo
KJKarl Anker Jørgensen
Karl Anker Jørgensen

5 October 2006 in Chemical Communications
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Journal Article
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Armando CarloneArmando Carlone
Armando Carlone
MMMauro Marigo
Mauro Marigo
CNChris North
Chris North
ALAitor Landa
Aitor Landa
KJKarl Anker Jørgensen
Karl Anker Jørgensen
Optically active 2,5-disubstituted-cyclohexen-2-one derivatives have been prepared in a one-pot process consisting of five reaction steps: an organocatalytic asymmetric conjugated addition of β-ketoesters to α,β-unsaturated aldehydes that proceeds in aqueous solutions or under solvent-free conditions has been implemented in a multi-step process.