Laura Palombi

Prof. Laura Palombi

Dipartimento di Chimica e Biologia, Università di Salerno, Via Giovanni Paolo II, 132, 84084-Fisciano, SA, Italy
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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1 October 2012 in Current Organic Chemistry
Verified
Journal Article
Closed access
AMAntonio Massa
Antonio Massa
Laura PalombiLaura Palombi
Laura Palombi
Antonio MassaAntonio Massa
Antonio Massa
Molecules containing 3-substituted isobenzofuranones and isoindolinones skeletons are found in important bioactive compounds and in a number of natural products. As a consequence several synthetic strategies, both asymmetric and non-asymmetric, have been developed. Thus, this review focuses on the main synthetic approaches to obtain these classes of compounds, analysing the common features, the scope and the limitations and at the same time giving particular emphasis to the role of active methylene compounds.

21 January 2003 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
Marta FerociMarta Feroci
Marta Feroci
MCMaria Antonietta Casadei
Maria Antonietta Casadei
MOMonica Orsini
Monica Orsini
Laura PalombiLaura Palombi
Laura Palombi
AIAchille Inesi
Achille Inesi

15 December 2015 in Beilstein Journal of Organic Chemistry
Verified
Journal Article
Open access
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AMAntonio Massa
Antonio Massa
MTMaximilian Tiffner
Maximilian Tiffner
FSFrancesco Scorzelli
Francesco Scorzelli
Laura PalombiLaura Palombi
Laura Palombi
RFRosanna Filosa
Rosanna Filosa
Antonio MassaAntonio Massa
Antonio Massa
New bifunctional chiral ammonium salts were investigated in an asymmetric cascade synthesis of a key building block for a variety of biologically relevant isoindolinones. With this chiral compound in hand, the development of further transformations allowed for the synthesis of diverse derivatives of high pharmaceutical value, such as the Belliotti (S)-PD172938 and arylated analogues with hypnotic sedative activity, obtained in good overall total yield (50%) and high enantiomeric purity (95% ee). The synthetic routes developed herein are particularly convenient in comparison with the current methods available in literature and are particularly promising for large scale applications.

1 September 2008 in Tetrahedron: Asymmetry
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Journal Article
Closed access
ASArrigo Scettri
Arrigo Scettri
Antonio MassaAntonio Massa
Antonio Massa
Laura PalombiLaura Palombi
Laura Palombi
RVRosaria Villano
Rosaria Villano
Maria Rosaria AcocellaMaria Rosaria Acocella
Maria Rosaria Acocella

1 August 2002 in Tetrahedron Letters
Verified
Journal Article
Closed access
Marta FerociMarta Feroci
Marta Feroci
AGArmando Gennaro
Armando Gennaro
AIAchille Inesi
Achille Inesi
MOMonica Orsini
Monica Orsini
Laura PalombiLaura Palombi
Laura Palombi

9 August 2012 in European Journal of Organic Chemistry
Verified
Journal Article
Closed access
PDF file
CPCarmen Petronzi
Carmen Petronzi
SCSelene Collarile
Selene Collarile
GCGianluca Croce
Gianluca Croce
RFRosanna Filosa
Rosanna Filosa
PCPaolo De Caprariis
Paolo De Caprariis
Antonio MassaAntonio Massa
Antonio Massa