Magnesium bis(monoperoxyphthalate) hexahydrate as mild and efficient oxidant for the synthesis of selenones

• Andrea Temperini,
• Massimo Curini,
• Ornelio Rosati and
• Lucio Minuti

Beilstein J. Org. Chem. 2014, 10, 1267–1271, doi:10.3762/bjoc.10.127

• Andrea Temperini Massimo Curini Ornelio Rosati Lucio Minuti Dipartimento di Scienze Farmaceutiche, Università di Perugia, via del Liceo 1, 06123 Perugia, Italy Dipartimento di Chimica, Biologia e Biotecnologia, Università di Perugia, via Elce di Sotto 8, 06123 Perugia, Italy 10.3762/bjoc.10.127

One-pot cross-enyne metathesis (CEYM)–Diels–Alder reaction of gem-difluoropropargylic alkynes

• Santos Fustero,
• Paula Bello,
• Javier Miró,
• María Sánchez-Roselló,
• Günter Haufe and
• Carlos del Pozo

Beilstein J. Org. Chem. 2013, 9, 2688–2695, doi:10.3762/bjoc.9.305

• Santos Fustero Paula Bello Javier Miro Maria Sanchez-Rosello Gunter Haufe Carlos del Pozo Departamento de Química Orgánica, Universidad de Valencia, E-46100 Burjassot, Spain Laboratorio de Moléculas Orgánicas, Centro de Investigación Príncipe Felipe, E-46012 Valencia, Spain Organisch-Chemisches

Synthetic scope and DFT analysis of the chiral binap–gold(I) complex-catalyzed 1,3-dipolar cycloaddition of azlactones with alkenes

• María Martín-Rodríguez,
• Luis M. Castelló,
• Carmen Nájera,
• José M. Sansano,
• Olatz Larrañaga,
• Abel de Cózar and
• Fernando P. Cossío

Beilstein J. Org. Chem. 2013, 9, 2422–2433, doi:10.3762/bjoc.9.280

• , Universidad del País Vasco, Apdo. 1072, E-20018 San Sebastián, Spain IKERBASQUE, Basque Foundation for Science, 48011 Bilbao, Spain 10.3762/bjoc.9.280 Abstract The 1,3-dipolar cycloaddition between glycine-derived azlactones with maleimides is efficiently catalyzed by the dimeric chiral complex [(Sa

Synthesis of enantiopure sugar-decorated six-armed triptycene derivatives

• Paola Bonaccorsi,
• Maria Luisa Di Gioia,
• Antonella Leggio,
• Lucio Minuti,
• Teresa Papalia,
• Carlo Siciliano,
• Andrea Temperini and
• Anna Barattucci

Beilstein J. Org. Chem. 2013, 9, 2410–2416, doi:10.3762/bjoc.9.278

• Nutrizione, Università della Calabria, Edificio Polifunzionale, 87030 Arcavacata di Rende, Italy Dipartimento di Chimica, Università di Perugia, via Elce di Sotto 8, 06123 Perugia, Italy Dipartimento di Scienze del Farmaco e Prodotti per la Salute, Università di Messina, villaggio SS. Annunziata, 98168

• Messina, Italy Dipartimento di Chimica e Tecnologia del Farmaco, Università di Perugia, via del Liceo 1, 06123 Perugia, Italy 10.3762/bjoc.9.278 Abstract A new class of molecules with a triptycene rigid core surrounded by six monosaccharide residues was synthesized. Hexakis(bromomethyl) substituted

One-pot sequential synthesis of isocyanates and urea derivatives via a microwave-assisted Staudinger–aza-Wittig reaction

• Diego Carnaroglio,
• Katia Martina,
• Giovanni Palmisano,
• Andrea Penoni,
• Claudia Domini and
• Giancarlo Cravotto

Beilstein J. Org. Chem. 2013, 9, 2378–2386, doi:10.3762/bjoc.9.274

• Diego Carnaroglio Katia Martina Giovanni Palmisano Andrea Penoni Claudia Domini Giancarlo Cravotto Dipartimento di Scienza e Tecnologia del Farmaco, University of Turin, Via Pietro Giuria 9, 10125 Torino, Italy; Fax +390116707687; Tel: +390116707684 Dipartimento di Scienza e Alta Tecnologia

• , University of Insubria, Via Valleggio 11, 22100 Como, Italy Department of Chemistry, Universidad Nacional del Sur, Av. Alem 1253, B8000CPB, Bahía Blanca, Buenos Aires, Argentina 10.3762/bjoc.9.274 Abstract A fast and efficient protocol for the synthesis of N,N'-disubstituted urea derivatives from alkyl

Structure of 1,5-benzodiazepinones in the solid state and in solution: Effect of the fluorination in the six-membered ring

• Marta Pérez-Torralba,
• Rosa M. Claramunt,
• M. Ángeles García,
• Concepción López,
• M. Carmen Torralba,
• M. Rosario Torres,
• Ibon Alkorta and
• José Elguero

Beilstein J. Org. Chem. 2013, 9, 2156–2167, doi:10.3762/bjoc.9.253

• Marta Perez-Torralba Rosa M. Claramunt M. Angeles Garcia Concepcion Lopez M. Carmen Torralba M. Rosario Torres Ibon Alkorta Jose Elguero Departamento de Química Orgánica y Bio-Orgánica, Facultad de Ciencias, UNED, Paseo Senda del Rey 9, 28040-Madrid, Spain Departamento de Química Inorgánica I and

True and masked three-coordinate T-shaped platinum(II) intermediates

• Manuel A. Ortuño,
• Salvador Conejero and
• Agustí Lledós

Beilstein J. Org. Chem. 2013, 9, 1352–1382, doi:10.3762/bjoc.9.153

• Manuel A. Ortuno Salvador Conejero Agusti Lledos Departament de Química, Universitat Autònoma de Barcelona, 08193 Cerdanyola del Vallès, Spain Instituto de Investigaciones Químicas (IIQ), Departamento de Química Inorgánica, CSIC and Universidad de Sevilla, Avda. Américo Vespucio 49, 41092 Sevilla

Inter- and intramolecular enantioselective carbolithiation reactions

• Asier Gómez-SanJuan,
• Nuria Sotomayor and
• Esther Lete

Beilstein J. Org. Chem. 2013, 9, 313–322, doi:10.3762/bjoc.9.36

• Asier Gomez-SanJuan Nuria Sotomayor Esther Lete Departamento de Química Orgánica II, Facultad de Ciencia y Tecnología, Universidad del País Vasco / Euskal Herriko Unibertsitatea UPV/EHU, Apdo. 644, 48080 Bilbao, Spain 10.3762/bjoc.9.36 Abstract In this review we summarize recent developments in

• ethers. Formation of six-membered rings: pyrroloisoquinolines. Formation of six-membered rings: tetrahydroquinolines. Acknowledgements We wish to thank the Ministerio de Ciencia e Innovación (CTQ2009-07733) and Universidad del País Vasco/Euskal Herriko Unibertsitatea (UFI11/22, GIU 0946) for their

Cyclodextrin-based nanosponges as drug carriers

• Francesco Trotta,
• Marco Zanetti and
• Roberta Cavalli

Beilstein J. Org. Chem. 2012, 8, 2091–2099, doi:10.3762/bjoc.8.235

• Francesco Trotta Marco Zanetti Roberta Cavalli Dipartimento di Chimica. University of Torino, Via Pietro Giuria 7 10125 Torino, Italy Dipartimento di Scienza e Tecnologia del Farmaco. University of Torino, Via Pietro Giuria 9 10125 Torino, Italy 10.3762/bjoc.8.235 Abstract Cyclodextrin-based

Reductive amination with zinc powder in aqueous media

• Giovanni B. Giovenzana,
• Daniela Imperio,
• Andrea Penoni and
• Giovanni Palmisano

Beilstein J. Org. Chem. 2011, 7, 1095–1099, doi:10.3762/bjoc.7.125

• Giovanni B. Giovenzana Daniela Imperio Andrea Penoni Giovanni Palmisano DiSCAFF, Università degli Studi del Piemonte Orientale “A. Avogadro”, Via Bovio 6, I-28100 Novara, Italy; Fax: +39-(0)321-375821, Tel: +39-(0)321-375846 Dipartimento di Scienze Chimiche e Ambientali, Università dell’Insubria

Chiral gold(I) vs chiral silver complexes as catalysts for the enantioselective synthesis of the second generation GSK-hepatitis C virus inhibitor

• María Martín-Rodríguez,
• Carmen Nájera,
• José M. Sansano,
• Abel de Cózar and
• Fernando P. Cossío

Beilstein J. Org. Chem. 2011, 7, 988–996, doi:10.3762/bjoc.7.111

• Maria Martin-Rodriguez Carmen Najera Jose M. Sansano Abel de Cozar Fernando P. Cossio Departamento de Química Orgánica e Instituto de Síntesis Orgánica, Universidad de Alicante, Apdo. 99, E-03080 Alicante, Spain Departamento de Química Orgánica I, Facultad de Química, Universidad del País Vasco

EPR and pulsed ENDOR study of intermediates from reactions of aromatic azides with group 13 metal trichlorides

• Giorgio Bencivenni,
• Riccardo Cesari,
• Daniele Nanni,
• Hassane El Mkami and
• John C. Walton

Beilstein J. Org. Chem. 2010, 6, 713–725, doi:10.3762/bjoc.6.84

• Giorgio Bencivenni Riccardo Cesari Daniele Nanni Hassane El Mkami John C. Walton Dipartimento di Chimica Organica “A. Mangini”, Università di Bologna, Viale del Risorgimento 4, Bologna I-40136, Italy School of Physics and Astronomy, University of St. Andrews, St. Andrews, Fife KY16 9SS, UK School

Facile synthesis of two diastereomeric indolizidines corresponding to the postulated structure of alkaloid 5,9E- 259B from a Bufonid toad (Melanophryniscus)

• Angela Nelson,
• H. Martin Garraffo,
• Thomas F. Spande,
• John W. Daly and
• Paul J. Stevenson

Beilstein J. Org. Chem. 2008, 4, No. 6, doi:10.1186/1860-5397-4-6

• the Department of Education and Learning DEL for a studentship to Angela Nelson. The research at NIH was supported by the intramural funds of NIDDK.