S. Serra

发表

Final Demonstration of the Co-Identity of Lipiarmycin A3 and Tiacumicin B (Fidaxomicin) through Single Crystal X-ray Analysis

C. Fuganti, S. Serra, L. Malpezzi, 2017, Antibiotics.

The Co-identity of Lipiarmycin A3 and Tiacumicin B

C. Fuganti, S. Serra, A. Bedeschi, 2014, Natural product communications.

Chemoenzymatic resolution of cis- and trans-3,6-dihydroxy-α-ionone. Synthesis of the enantiomeric forms of dehydrovomifoliol and 8,9-dehydrotheaspirone

C. Fuganti, S. Serra, A. Barakat, 2007 .

Enzymatic approach to enantiomerically pure 5-alken-2,4-diols and 4-hydroxy-5-alken-2-ones: application to the synthesis of chiral synthons.

E. Brenna, F. Gatti, Agnese Abate, 2006, The Journal of organic chemistry.

Lipase-catalysed synthesis of homotartaric acid enantiomers

E. Brenna, F. Gatti, C. Fuganti, 2009 .

Baker's Yeast Reduction of β‐Hydroxy Ketones

E. Brenna, F. Gatti, C. Fuganti, 2010 .

Lipase-catalysed preparation of enantiomerically enriched odorants

E. Brenna, F. Gatti, Agnese Abate, 2004 .

Odor and (Bio)diversity: Single Enantiomers of Chiral Fragrant Substances

E. Brenna, F. Gatti, Agnese Abate, 2004, Chemistry & biodiversity.

Exploitation of Soybean Oil Acid Degumming Waste: Biocatalytic Synthesis of High Value Phospholipids

Chiara Allegretti, Davide Tessaro, P. D’Arrigo, 2021, ChemistrySelect.

Valorization of Corn Seed Oil Acid Degumming Waste for Phospholipids Preparation by Phospholipase D-Mediated Processes

Chiara Allegretti, Davide Tessaro, P. D’Arrigo, 2020, Catalysts.

From commercial racemic fragrances to odour active enantiopure compounds: the ten isomers of irone

E. Brenna, C. Fuganti, S. Serra, 2003 .

Studies on the Synthesis of Highly Substituted Naphthol: Preparation of 6-Hydroxy-5,7-dimethoxy-2-naphthoic Acid, Isolated from Ulmus Thomasii

C. Fuganti, S. Serra, 1998 .

Opportunities for Biocatalysis in the Flavor, Fragrance, and Cosmetic Industry

S. Serra, 2011 .

Baker's yeast-mediated approach to (−)-cis- and (+)-trans-Aerangis lactones

E. Brenna, C. Fuganti, S. Serra, 2001 .

A General Synthetic Approach to Hydroquinone Meroterpenoids: Stereoselective Synthesis of (+)-(S)-Metachromin V and Alliodorol

A. Cominetti, S. Serra, Veronica Lissoni, 2014, Natural product communications.

Reactive Deep Eutectic Solvents (RDESs): A New Tool for Phospholipase D-Catalyzed Preparation of Phospholipids

Chiara Allegretti, P. D’Arrigo, F. Gatti, 2021, Catalysts.

Towards a Complete Exploitation of Brewers’ Spent Grain from a Circular Economy Perspective

G. Griffini, S. Turri, Chiara Allegretti, 2022, Fermentation.

3 Biotechnological Tools to Produce Natural Flavors and Methods to Authenticate Their Origin

E. Brenna, F. Gatti, C. Fuganti, 2010 .

Two Complementary Synthetic Approaches to the Enantiomeric Forms of the Chiral Building Block (2,6,6-Trimethyltetrahydro-2H-pyran-2-yl)methanol: Application to the Stereospecific Preparation of the Natural Flavor Linaloyl Oxide

S. Serra, D. De Simeis, 2018, Catalysts.

The Positionalδ(18O) Values of Extracted and Synthetic Vanillin

F. Reniero, C. Guillou, C. Fuganti, 2001 .

Recent Advances in the Synthesis of Carotenoid-Derived Flavours and Fragrances

S. Serra, 2015, Molecules.

Stereochemical Course of Baker's Yeast Mediated Reduction of the Tri‐ and Tetrasubstituted Double Bonds of Substituted Cinnamaldehydes

C. Fuganti, S. Serra, G. Fronza, 2009 .

Preparation of the Enantiomerically Enriched Isomers of the Odorous Cyclic Ethers Clarycet®, Florol®, and Rhubafuran® by Enzymatic Catalysis

E. Brenna, F. Gatti, Agnese Abate, 2004 .

Oxidation of Terpenoids to Achieve High-Value Flavor and Fragrances—Questioning Microalgae Oxidative Capabilities in the Biotransformation of the Sesquiterpene Valencene and of Selected Natural Apocarotenoids

S. Serra, F. Secundo, D. De Simeis, 2021, Chemistry.

Bacterial Biotransformation of Oleic Acid: New Findings on the Formation of γ-Dodecalactone and 10-Ketostearic Acid in the Culture of Micrococcus luteus †

E. Brenna, S. Serra, D. De Simeis, 2020, Molecules.

A Practical Laboratory-Scale Synthesis of All Eight Stereoisomeric Forms of Terpene Linalool Oxide

S. Serra, D. De Simeis, Sara Papili, 2021, Chemistry.

Lipase mediated resolution of cis- and trans-linalool oxide (pyranoid)

E. Brenna, S. Serra, Davide De Simeis, 2016 .

A Study on the Lipase-catalysed Acylation of 6,7-Dihydroxy-linalool

S. Serra, D. De Simeis, 2016, Natural product communications.

Enantioselective perception of chiral odorants

E. Brenna, C. Fuganti, S. Serra, 2003 .

delta(13)C- and delta(18)O-values of glycerol of food fats.

F. Reniero, C. Guillou, C. Fuganti, 2001, Rapid communications in mass spectrometry : RCM.

Stereoselective Synthesis of Terpenoids through Lipase-Mediated Resolution Approaches

S. Serra, D. De Simeis, 2020, Catalysts.

Synthesis of 2,3-Dihydro-6-methylthieno[2,3-c]furan (Kahweofuran), a Coffee Aroma Component, from an Acyclic Precursor

E. Brenna, C. Fuganti, S. Serra, 1998 .

Biocatalytic methods for the synthesis of enantioenriched odor active compounds.

E. Brenna, F. Gatti, C. Fuganti, 2011, Chemical reviews.

Lipase-mediated resolution of substituted 2-aryl-propanols: application to the enantioselective synthesis of phenolic sesquiterpenes

S. Serra, 2011 .

Biocatalysed synthesis of the enantiomers of the floral odorant Florhydral

E. Brenna, Agnese Abate, C. Fuganti, 2002 .

Enzyme-Mediated Stereoselective Synthesis

S. Serra, 2019, Catalysts.

Biocatalytic Methods for the Synthesis of Enantioenriched Odor Active Compounds

E. Brenna, F. Gatti, C. Fuganti, 2011 .

Biocatalytic preparation of natural flavours and fragrances.

E. Brenna, C. Fuganti, S. Serra, 2005, Trends in biotechnology.

Fungi-Mediated Biotransformation of the Isomeric Forms of the Apocarotenoids Ionone, Damascone and Theaspirane

Stefano Serra, S. Serra, Davide De Simeis, 2018, Molecules.

Enzyme-Mediated Synthesis of Sesquiterpenes

S. Serra, 2015, Natural product communications.

Baker’s yeast mediated enantioselective synthesis of the bisabolane sesquiterpenes curcumene, turmerone, dehydrocurcumene and nuciferal

C. Fuganti, S. Serra, Andrea Dulio, 1999 .

A new approach to 2-aryl-7-alkoxy-benzofurans: Synthesis of ailanthoidol, a natural neolignan

C. Fuganti, S. Serra, 1998 .

Preparation and use of enantioenriched 2-aryl-propylsulfonylbenzene derivatives as valuable building blocks for the enantioselective synthesis of bisabolane sesquiterpenes

S. Serra, 2014 .

A New Preparative Route to Substituted Carbazoles by Benzannulation

C. Fuganti, S. Serra, 2005 .

Saponaceolides: Differential cytotoxicity and enantioselective synthesis of the right-hand lactone moiety

G. Vidari, S. Serra, G. Lanfranchi, 1995 .

A general method for the synthesis of the most powerful naturally occurring Maillard flavors

F. Gatti, C. Fuganti, S. Serra, 2007 .

On the baker's yeast mediated transformation of α-bromoenones. Synthesis of (1S,2R)-2-bromoindan-1-ol and (2S,3S)-3-bromo-4-phenylbutan-2-ol

C. Fuganti, S. Serra, G. Fronza, 1998 .

Enantioselective perception of chiral odorants

E. Brenna, C. Fuganti, S. Serra, 2003 .

Actinomycetes: A Never-Ending Source of Bioactive Compounds—An Overview on Antibiotics Production

S. Serra, D. De Simeis, Davide De Simeis, 2021, Antibiotics.

A new two step route to 1-hydroxy-9H-3-carbazolecarboxylic acid derivatives from 3-formylindole. Application to the synthesis of mukonine

E. Brenna, C. Fuganti, S. Serra, 1998 .

Recent advances in the benzannulation of substituted 3-alkoxycarbonyl-3,5-hexadienoic acids and 3-alkoxycarbonylhex-3-en-5-ynoic acids to polysubstituted aromatics.

Elisabetta Brenna, Stefano Serra, Claudio Fuganti, 2007, Chemistry.

RECENT PROGRESS ON THE ITERATIVE CONSTRUCTION OF 4-SUBSTITUTED-3-HYDROXY BENZOIC ACIDS FROM UNSATURATED ALDEHYDES AND DIMETHYL SUCCINATE

E. Brenna, C. Fuganti, S. Serra, 1997 .

Stable isotope characterization of raspberry ketone extracted from Taxus baccata and obtained by oxidation of the accompanying alcohol (Betuligenol).

F. Reniero, C. Guillou, C. Fuganti, 1999, Journal of agricultural and food chemistry.

MnO2/TBHP: A Versatile and User‐Friendly Combination of Reagents for the Oxidation of Allylic and Benzylic Methylene Functional Groups

S. Serra, 2015 .

Enantioselective synthesis of benzylic stereocentres via Claisen rearrangement of enantiomerically pure allylic alcohols: preparation of (R)- and (S)-3-methyl-2-phenylbutylamine

E. Brenna, F. Gatti, C. Fuganti, 2003 .

Synthesis of the enantiomeric forms of α- and γ-damascone starting from commercial racemic α-ionone

C. Fuganti, S. Serra, 2006 .

A General Strategy for the Stereoselective Synthesis of the Furanosesquiterpenes Structurally Related to Pallescensins 1–2

S. Serra, 2019, Marine drugs.

A new chemo-enzymatic approach to the stereoselective synthesis of the flavors tetrahydroactinidiolide and dihydroactinidiolide

S. Serra, Omar Piccioni, 2015 .

Synthesis of L‐ and D‐4,6‐Dideoxyhexoses and 4,6‐Dideoxy‐C‐phenylglycosides from Enzyme‐Generated Products

E. Brenna, F. Gatti, C. Fuganti, 2008 .

Synthesis, Olfactory Evaluation, and Determination of the Absolute Configuration of the 3,4-Didehydroionone Stereoisomers

E. Brenna, C. Fuganti, S. Serra, 2006 .

Enantioselective synthesis of cis-7-methoxy-calamenene via Claisen rearrangement of an enzymatically resolved allyl alcohol

E. Brenna, F. Gatti, C. Fuganti, 2004 .

Baker’s yeast-mediated enantioselective synthesis of the bisabolane sesquiterpenes (+)-curcuphenol, (+)-xanthorrhizol, (−)-curcuquinone and (+)-curcuhydroquinone

C. Fuganti, S. Serra, 2000 .

Recent Developments in the Synthesis of the Flavors and Fragrances of Terpenoid Origin

S. Serra, 2015 .

Lipase-mediated resolution of the hydroxy-cyclogeraniol isomers: application to the synthesis of the enantiomers of karahana lactone, karahana ether, crocusatin C and γ-cyclogeraniol

F. Gatti, C. Fuganti, S. Serra, 2009 .

Synthesis and Olfactory Evaluation of (+)- and (-)-gamma-Ionone

C. Fuganti, S. Serra, A. Zenoni, 2000 .

3-Alkyl-p-menthan-3-ol derivatives : synthesis and evaluation of their physiological cooling activity

A. Vecchione, C. Fuganti, S. Serra, 2008 .

p‐Menthandiol‐vanillin acetals: synthesis and study of their chemo‐sensorial properties

G. Ottolina, F. Gatti, A. Cominetti, 2014 .

Enantioselective Synthesis of Natural Trinorsesquiterpene Tetralones by Chemo-enzymatic Approaches

S. Serra, 2013, Natural product communications.

A Chemoenzymatic, Preparative Synthesis of the Isomeric Forms of p‐Menth‐1‐en‐9‐ol: Application to the Synthesis of the Isomeric Forms of the Cooling Agent 1‐Hydroxy‐2,9‐cineole

F. Gatti, C. Fuganti, S. Serra, 2008 .

Baker′s Yeast Mediated Enantioselective Synthesis of the Bisabolane Sesquiterpenes Curcumene, Turmerone, Dehydrocurcumene and Nuciferal.

C. Fuganti, S. Serra, Andrea Dulio, 1999 .

Chemoenzymatic preparation of the p-menth-1,5-dien-9-ol stereoisomers and their use in the enantiospecific synthesis of natural p-menthane monoterpenes

S. Serra, Igor Nobile, 2011 .

Enzyme‐Mediated Synthesis of (S)‐ and (R)‐Verapamil

E. Brenna, C. Fuganti, P. Grasselli, 2001 .

Stereochemical Outcome of the Biocatalysed Reduction of Activated Tetrasubstituted Olefins by Old Yellow Enzymes 1–3

F. Parmeggiani, D. Monti, E. Brenna, 2012 .

Baker's yeast mediated biohydrogenation of sulphur-functionalised methacrolein derivatives. Stereochemical aspects of the reaction and preparation of the two enantiomers of useful C4 bifunctional chiral synthons

C. Fuganti, S. Serra, 2001 .

Chirality and fragrance chemistry: stereoisomers of the commercial chiral odorants Muguesia and Pamplefleur.

E. Brenna, F. Gatti, Agnese Abate, 2005, The Journal of organic chemistry.

Stereochemical aspects of the bioreduction of the conjugated double bond of perillaldehyde

C. Fuganti, S. Serra, G. Fronza, 2004 .

Synthesis and olfactory evaluation of all stereoisomers of the fragrance Nectaryl

E. Brenna, F. Gatti, C. Fuganti, 2008 .

Two Biotechnological Approaches to the Preparative Synthesis of Natural Dihydrocoumarin

S. Serra, Stefano Marzorati, Mattia Valentino, 2021, Catalysts.

Baker′s Yeast Mediated Biohydrogenation of Sulfur-Functionalized Methacrolein Derivatives. Stereochemical Aspects of the Reaction and Preparation of the Two Enantiomers of Useful C4 Bifunctional Chiral Synthons.

C. Fuganti, S. Serra, 2002 .

Enzyme-Mediated Syntheses of the Enantiomers of γ-Irones

E. Brenna, C. Fuganti, S. Serra, 2001 .

Lipase-mediated synthesis of the enantiomeric forms of 4,5-epoxy-4,5-dihydro-α-ionone and 5,6-epoxy-5,6-dihydro-β-ionone. A new direct access to enantiopure (R)- and (S)-α-ionone

E. Brenna, C. Fuganti, S. Serra, 1999 .

Enzyme-mediated synthesis of (R)- and (S)-α-ionone

E. Brenna, C. Fuganti, P. Grasselli, 1998 .

New developments in yeast extracts for use as flavour enhancers

S. Serra, 2007 .

Odor and (Bio)diversity: Single Enantiomers of Chiral Fragrant Substances

E. Brenna, F. Gatti, Agnese Abate, 2004, Chemistry & biodiversity.

Enzyme-catalysed approach to the preparation of triazole antifungals: synthesis of (−)-genaconazole

E. Brenna, F. Gatti, C. Fuganti, 2009 .

Optically Active Ionones and Derivatives: Preparation and Olfactory Properties

E. Brenna, C. Fuganti, S. Serra, 2002 .

Aromatic annulation on the p-menthane monoterpenes: enantiospecific synthesis of the trans and cis isomers of calamenene and 8-hydroxycalamenene

C. Fuganti, S. Serra, 2005 .

A divergent and stereoselective approach to phenolic 1,7-dihydroxy-bisabolane sesquiterpenes: asymmetric total synthesis of (+)-curcutetraol, (+)-sydonol, (+)-sydonic acid, and (+)-7-O-methylsydonic acid

A. Cominetti, S. Serra, 2013 .

Bisabolane Sesquiterpenes: Synthesis of (R)-(+)-Sydowic Acid and (R)-(+)-Curcumene Ether.

S. Serra, 2000 .

Bisabolane Sesquiterpenes: Synthesis of (R)-(+)-Sydowic Acid and (R)-(+)-Curcumene Ether

S. Serra, 2000 .

A Divergent and Stereoselective Approach to Phenolic 1,7-Dihydroxy-bisabolane Sesquiterpenes: Asymmetric Total Synthesis of (+)-Curcutetraol (Ia), (+)-Sydonol (Ib), (+)-Sydonic Acid (Ic), and (+)-7-O-Methylsydonic Acid (Id).

A. Cominetti, S. Serra, 2014 .

Unambiguous Characterization of the Sesquiterpene (7R,9E)‐1,2,11‐Trihydroxy‐1,3,5,9‐bisabolatetraene through Its Enantioselective Synthesis

S. Serra, G. Fronza, 2012 .

Enantioselective Synthesis of the Bisabolane Sesquiterpene (+)-1-Hydroxy-1,3,5-Bisabolatrien-10-one and Revision of its Absolute Configuration

S. Serra, 2012, Natural product communications.

CUPARENE SESQUITERPENES: SYNTHESIS OF (+)-3-HYDROXYCUPARENE AND (+)-CUPARENE

C. Fuganti, S. Serra, 1999 .

A Concise Synthesis of 3-Hydroxy-4-(β-glucopyranosyl) Benzoate: A New Route to β-C-Aryl Glycosides

C. Fuganti, S. Serra, 1999 .

Synthesis, olfactory evaluation and determination of the absolute configuration of the β- and γ-Iralia® isomers

E. Brenna, C. Fuganti, S. Serra, 2008 .

Enzymatic Approach to and Odor Description of the Twelve Enantiomerically Pure Isomers of Pelargene

E. Brenna, F. Gatti, Agnese Abate, 2006 .

Applications of biocatalysis in fragrance chemistry: the enantiomers of alpha-, beta-, and gamma-irones.

E. Brenna, C. Fuganti, S. Serra, 2008, Chemical Society reviews.

The enantiomers of Iralia® : preparation and odour evaluation

E. Brenna, Agnese Abate, C. Fuganti, 2007 .

Synthesis and olfactory evaluation of the enantiomerically enriched forms of 7,11-epoxymegastigma-5(6)-en-9-one and 7,11-epoxymegastigma-5(6)-en-9-ols isomers, identified in Passiflora edulis

E. Brenna, C. Fuganti, S. Serra, 2005 .

Enzyme-mediated synthesis of new 1,3-dioxane odorants related to Floropal

E. Brenna, Agnese Abate, C. Fuganti, 2004 .

Natural p‐Menthene Monoterpenes: Synthesis of the Enantiomeric Forms of Wine Lactone, Epi‐wine Lactone, Dill Ether, and Epi‐dill Ether Starting from a Common Intermediate

C. Fuganti, S. Serra, 2004 .

Enzyme‐Mediated Preparation of Chiral 1,3‐Dioxane Odorants

E. Brenna, Agnese Abate, C. Fuganti, 2003 .

Enzyme-Mediated Preparation of Enantiomerically Pure p-Menthan- 3,9-diols and Their Use for the Synthesis of Natural p-Menthane Lactones and Ethers

C. Fuganti, S. Serra, 2002 .

Enzyme-Mediated Preparation of (+)- and (−)-β-Irone and (+)- and (−)-cis-γ-Irone fromIrone alpha®

E. Brenna, C. Fuganti, S. Serra, 2001 .

Enzyme‐Mediated Preparation of (+)‐ and (–)‐cis‐α‐Irone and (+)‐ and (–)‐trans‐α‐Irone

E. Brenna, C. Fuganti, S. Serra, 1999 .

Enzyme‐Mediated Preparation of the Single Enantiomers of the Olfactory Active Components of the Woody Odorant Timberol®

E. Brenna, C. Fuganti, S. Serra, 1999 .

Two easy photochemical methods for the conversion of commercial ionone alpha into regioisomerically enriched γ‐ionone and γ‐dihydroionone

E. Brenna, C. Fuganti, S. Serra, 2007 .

Natural flavor ester synthesis catalyzed by lipases

S. Riva, Xiangzhao Mao, S. Serra, 2020 .

Applications of Biocatalysis in Fragrance Chemistry: The Enantiomers of α-, β-, and γ-Irones

E. Brenna, C. Fuganti, S. Serra, 2009 .

Acetylation of Racemic cis‐ and trans‐α‐Irols, Mediated by Porcine Pancreatic Lipase (PPL) − A New Route to (−) and (+)‐cis‐α‐Irone

E. Brenna, C. Fuganti, S. Serra, 2000 .

An Expedient Synthesis of Linden Ether

A. Cominetti, S. Serra, 2014, Natural product communications.

Preparation of the enantiomeric forms of wine lactone, epi-wine lactone, dill ether and epi-dill ether

C. Fuganti, S. Serra, 2006 .

Lipase-catalyzed resolution of p-menthan-3-ols monoterpenes: preparation of the enantiomer-enriched forms of menthol, isopulegol, trans- and cis-piperitol, and cis-isopiperitenol

E. Brenna, C. Fuganti, S. Serra, 2003 .

Changing the Odor Properties of Commercial Mixtures of α-Irones by Simple Chemical Transformations

E. Brenna, C. Fuganti, S. Serra, 2004 .

An expedient preparation of enantio‐enriched ambergris odorants starting from commercial ionone alpha

S. Serra, 2013 .

Enantioselective enzymatic resolution of racemic alcohols by lipases in green organic solvents

S. Serra, F. Secundo, Z. Djeghaba, 2017 .

Biocatalyzed preparation of the optically enriched stereoisomers of 4-methyl-2-phenyl-tetrahydro-2H-pyran (Doremox®)

E. Brenna, C. Fuganti, S. Serra, 2002 .

New Stereoselective Synthesisof Paeonilactone B

F. Gatti, S. Serra, 2009 .

Enzyme-mediated preparation of enantioenriched forms of trans- and cis-p-menthan-1,8-dien-5-ol

E. Brenna, F. Gatti, C. Fuganti, 2006 .

First Enantioselective Synthesis of Marine Diterpene Ambliol‐A

S. Serra, Veronica Lissoni, 2015 .

Use of (S)-trans-γ-Monocyclofarnesol as a Useful Chiral Building Block for the Stereoselective Synthesis of Diterpenic Natural Products

A. Cominetti, S. Serra, Veronica Lissoni, 2014, Natural product communications.

Studies on the total synthesis of the saponaceolides. 1. Enantioselective synthesis of the spiroketal subunit

G. Vidari, S. Serra, G. Lanfranchi, 1999 .

Studies on the total synthesis of the saponaceolides. 2. Enantioselective synthesis of 2-epi-saponaceolide B

G. Vidari, S. Serra, G. Lanfranchi, 1999 .

Biocatalytic Synthesis of Natural Dihydrocoumarin by Microbial Reduction of Coumarin

S. Serra, A. Castagna, Mattia Valentino, 2019, Catalysts.

Oleate Hydratase from Lactobacillus rhamnosus ATCC 53103: A FADH2-Dependent Enzyme with Remarkable Industrial Potential

S. Serra, Stefano Marzorati, D. De Simeis, 2021, Catalysts.

Recombinant Oleate Hydratase from Lactobacillus rhamnosus ATCC 53103: Enzyme Expression and Design of a Reliable Experimental Procedure for the Stereoselective Hydration of Oleic Acid

D. Monti, E. E. Ferrandi, S. Serra, 2020, Catalysts.

The Fatty-Acid Hydratase Activity of the Most Common Probiotic Microorganisms

S. Serra, D. De Simeis, A. Castagna, 2020, Catalysts.

Use of Lactobacillus rhamnosus (ATCC 53103) as Whole-Cell Biocatalyst for the Regio- and Stereoselective Hydration of Oleic, Linoleic, and Linolenic Acid

S. Serra, Davide De Simeis, D. D. Simeis, 2018 .

New insights on the baker's yeast‐mediated hydration of oleic acid: the bacterial contaminants of yeast are responsible for the stereoselective formation of (R)‐10‐hydroxystearic acid

S. Serra, D. De Simeis, D. D. Simeis, 2018, Journal of applied microbiology.

Stable isotope characterization of the ortho-oxygenated phenylpropanoids: coumarin and melilotol.

F. Reniero, C. Guillou, E. Brenna, 2005, Journal of agricultural and food chemistry.

Differentiation of extractive and synthetic salicin. The 2H aromatic pattern of natural 2-hydroxybenzyl alcohol.

E. Brenna, F. Gatti, C. Fuganti, 2004, Journal of agricultural and food chemistry.

Regiospecific synthesis of heterosubstituted phenols from 3-alkoxycarbonyl-3,5-dienoic acids via benzannulation reaction.

C. Fuganti, S. Serra, S Serra, 2001, The Journal of organic chemistry.

A Practical, Enantiospecific Synthesis of (S)-Trans-γ-Monocyclofarnesol

S. Serra, 2012, Natural product communications.

Peptide-Mediated Targeted Delivery of Aloe-Emodin as Anticancer Drug

A. Stringaro, A. Vitali, A. Calcabrini, 2022, Molecules.

New synthetic approach to atypical retinoids: application of a versatile annulation procedure

E. Brenna, F. Gatti, C. Fuganti, 2007 .

Stereoselective Synthesis of 2,15-Dihydroxycalamenene and 2-Methoxycalamenene. Determination of the Configuration of Natural 2,15-Dihydroxycalamenene

S. Serra, 2015, Natural Product Communications.

Aromatic Annulation on the p-Menthane Monoterpenes: Enantiospecific Synthesis of the trans and cis Isomers of Calamenene and 8-Hydroxycalamenene.

C. Fuganti, S. Serra, 2005 .

Enzymes, Biocatalysis and Chemical Biology

S. Serra, 2020, Molecules.

Benzannulation of Substituted 3-Alkoxycarbonylhex-3-en-5-ynoic Acids: A New Route to 4-Substituted 3,5-Dihydroxybenzoic Acids Derivatives

C. Fuganti, S. Serra, 2002 .

New route to o-terphenyls: application to the synthesis of 6,7,10,11-tetramethoxy-2-(methoxycarbonyl)triphenylene

E. Brenna, C. Fuganti, S. Serra, 1998 .

New Route to o‐Terphenyls: Application to the Synthesis of 6,7,10,11‐Tetramethoxy‐2‐(methoxycarbonyl)triphenylene.

E. Brenna, C. Fuganti, S. Serra, 1998 .

Fractionation of Raw and Parboiled Rice Husks with Deep Eutectic Solvents and Characterization of the Extracted Lignins towards a Circular Economy Perspective

G. Griffini, S. Turri, Chiara Allegretti, 2022, Molecules.

A Practical and Efficient Process for the Preparation of Tazarotene

C. Fuganti, S. Serra, L. Malpezzi, 2005 .

Applications of biocatalysis in fragrance chemistry: the enantiomers of alpha-, beta-, and gamma-irones.

E. Brenna, C. Fuganti, S. Serra, 2008, Chemical Society reviews.

A new preparative route to substituted dibenzofurans by benzannulation reaction. An application to the synthesis of cannabifuran

C. Fuganti, S. Serra, 2003 .