Rosa Lanzetta

University of Naples Federico II

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Michelangelo Parrilli

University of Naples Federico II

204

Antonio Molinaro

University of Naples Federico II

152

Alba Silipo

University of Naples Federico II

Maria Michela Corsaro

University of Naples Federico II

Cristina De Castro

University of Naples Federico II

Domenico Garozzo

Institute of Polymers, Composites and Biomaterials

Antonio Evidente

National Research Council

Luisa Sturiale

Institute of Polymers, Composites and Biomaterials

Matteo Adinolfí

Guy's Hospital

Lorenzo Mangoni

University of Bayreuth

Cooperative Institutions

University of Naples Federico II

189

Federico II University Hospital

Istituto Nazionale di Fisica Nucleare, Sezione di Napoli

National Research Council

Istituto di Chimica Biomolecolare

Centre National de la Recherche Scientifique

Institute of Polymers, Composites and Biomaterials

University of Florence

University of Salerno

National Academies of Sciences, Engineering, and Medicine

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The steric course of iodine halogenide addition to 1-methy1-4-t-butylcyclohexene: Influence of iodinating species

Tetrahedron (1984)

Matteo Adinolfí Gaspare Barone Rosa Lanzetta G. Laonigro Lorenzo Mangoni

Nucleophilic Addition

10.1016/s0040-4020(01)88463-5

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Citations (3)

Linear precursors of liquid crystalline thermosets

Journal of Materials Chemistry (1996)

Barbara Hirn Cosimo Carfagna Rosa Lanzetta

Polycondensation of glutaric acid with a diglycidyl terminated mesogenic molecule [p-(2,3-epoxypropoxy)-α-methylstilbene] was carried out with a basic catalyst. A variety of novel main chain thermotropic liquid crystal oligoesters were synthesized via a short melt-copolycondensation process, by using different ratios of co-monomers. Preliminary studies by thermogravimetric analysis, differential scanning calorimetry, steric exclusion chromatography and Fourier transform infrared spectroscopy have been carried out on the reacting mixtures in order to optimize the reaction conditions (temperature, time). Carbon-13 nuclear magnetic resonance was used to identify the material structure. The mesophase stability ranges of the oligoesters were evaluated by means of DSC and optical polarizing microscopy. X-Ray diffraction analysis was applied to determine the nature of the mesophase.

Thermotropic crystal

Mesogen

Thermogravimetric analysis

10.1039/jm9960601473

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Citations (10)

The relative and absolute configurations of stereocenters in caryophyllose

Carbohydrate Research (1995)

Matteo Adinolfí Maria Michela Corsaro Cristina De Castro Antonio Evidente Rosa Lanzetta

Stereocenter

Absolute Configuration

Absolute (philosophy)

Diastereomer

10.1016/0008-6215(95)00127-f

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Citations (28)

Glycosides from Muscaricomosum. 4. Structure of muscaroside A

Canadian Journal of Chemistry (1983)

M. Adinolfi G. Barone Rosa Lanzetta G. Laonigro L. Mangoni

The less polar component of the glycoside mixture extracted from the bulbs of Muscaricomosum has been completely characterized. This glycoside, 5, possesses an α-L-rhamnopyranosyl(1→2)-β-D-glucopyranosyl(1→2)-α-L-arabinopyranosyl(1→6)-β-D-glucopyranosyl chain linked at the C-3 position of eucosterol 1.

10.1139/v83-452

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Citations (11)

Triterpenes from Bulbs of Muscari comosum, 4. The Structure of Further Novel Nortriterpene Components

Journal of Natural Products (1984)

Matteo Adinolfí G. Barone Rosa Lanzetta G. Laonigro Lorenzo Mangoni

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTTriterpenes from Bulbs of Muscari comosum, 4. The Structure of Further Novel Nortriterpene ComponentsM. Adinolfi, G. Barone, R. Lanzetta, G. Laonigro, L. Mangoni, and M. ParrilliCite this: J. Nat. Prod. 1984, 47, 4, 721–723Publication Date (Print):July 1, 1984Publication History Published online1 July 2004Published inissue 1 July 1984https://pubs.acs.org/doi/10.1021/np50034a029https://doi.org/10.1021/np50034a029research-articleACS PublicationsRequest reuse permissionsArticle Views71Altmetric-Citations7LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts

Terpene

Liliaceae

10.1021/np50034a029

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Citations (10)

Innate immunity probed by lipopolysaccharides affinity strategy and proteomics

Analytical and Bioanalytical Chemistry (2012)

Chiara Giangrande Lucia Colarusso Rosa Lanzetta Antonio Molinaro Piero Pucci

Pathogen-associated molecular pattern

Lipopolysaccharide binding protein

10.1007/s00216-012-6204-3

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Citations (10)

Cover Feature: Characterisation of the Dynamic Interactions between Complex N ‐Glycans and Human CD22 (ChemBioChem 1‐2/2020)

ChemBioChem (2019)

Cristina Di Carluccio Enrique Crisman Yoshiyuki Manabe Rosa Ester Forgione Alessandra Lacetera

Recognition and binding of host sialoglycans by human CD22. On resting B-cells, the cis interaction of h-CD22 with sialoglycans exposed on the same plasma membrane results in the formation of CD22 homo-oligomers. Conversely, trans interactions allow the recruitment of CD22 to the B-cell receptor complex, thereby inhibiting its signaling. In their full paper, S. Martín-Santamaría, R. Marchetti, A. Silipo, et al. on page 129 in Issue 1, 2020 (DOI: 10.1002/cbic.201900295) deepen the molecular insights into the binding mode and the conformation behavior of complex-type N-glycans bound to h-CD22. These new findings will enable the design of novel therapeutics with the aim of tackling autoimmune disorders and B-cell malignancies.

CD22

10.1002/cbic.201900762

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Citations (1)

Structure elucidation of the O-chain from the major lipopolysaccharide of the Xanthomonas campestris strain 642

Carbohydrate Research (2000)

Antonio Molinaro Antonio Evidente Stefania Fiore Nicola Sante Iacobellis Rosa Lanzetta

Strain (injury)

Xanthomonas

Pseudomonadales

Chemical structure

10.1016/s0008-6215(99)00333-x

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Citations (14)

The biofilm matrix of Pseudomonas sp. OX1 grown on phenol is mainly constituted by alginate oligosaccharides

Carbohydrate Research (2006)

Serena Leone Antonio Molinaro Fabiana Alfieri Valeria Cafaro Rosa Lanzetta

Matrix (chemical analysis)

Pseudomonadales

10.1016/j.carres.2006.06.011

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Citations (23)

Structural Analysis of the Deep Rough Lipopolysaccharide from Gram Negative Bacterium Alteromonas macleodii ATCC 27126^T: The First Finding of β‐Kdo in the Inner Core of Lipopolysaccharides

European Journal of Organic Chemistry (2006)

Valeria Liparoti Antonio Molinaro Luisa Sturiale Domenico Garozzo Evgeny L. Nazarenko

Abstract Alteromonas macleodii ATCC 27126 T is a Gram‐negative marine bacterium isolated from a sea water sample collected from around the Hawaiian Islands. The structure of the lipooligosaccharide derived from its outer membrane has been fully determined using either alkaline or acid hydrolysis. Alkaline treatment, aimed at recovering the complete carbohydrate backbone, was carried out by mild hydrazinolysis (de‐ O ‐acylation) followed by de‐ N ‐acylation using hot KOH and furnished a single core glycoform. Mild acid hydrolysis was employed to obtain the lipid A moiety which was selectively de‐ O ‐acylated and analysed to determine its primary structure. The structural elucidation of both fractions was carried out by chemical analyses, 2D NMR spectroscopy and MALDI‐TOF mass spectrometry and revealed a novel lipooligosaccharide with an unusual structure. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)

Alteromonas

Lipid A

Gram-Negative Bacteria

10.1002/ejoc.200600489

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Citations (18)