Azirinium ylides from α-diazoketones and 2H-azirines on the route to 2H-1,4-oxazines: three-membered ring opening vs 1,5-cyclization
- Nikolai V. Rostovskii,
- Mikhail S. Novikov,
- Alexander F. Khlebnikov,
- Galina L. Starova and
- Margarita S. Avdontseva
Beilstein J. Org. Chem. 2015, 11, 302–312, doi:10.3762/bjoc.11.35
An unusually stable chlorophosphite: What makes BIFOP–Cl so robust against hydrolysis?
- Roberto Blanco Trillo,
- Jörg M. Neudörfl and
- Bernd Goldfuss
Beilstein J. Org. Chem. 2015, 11, 313–322, doi:10.3762/bjoc.11.36
A simple and efficient method for the preparation of 5-hydroxy-3-acyltetramic acids
- Johanna Trenner and
- Evgeny V. Prusov
Beilstein J. Org. Chem. 2015, 11, 323–327, doi:10.3762/bjoc.11.37
C-5’-Triazolyl-2’-oxa-3’-aza-4’a-carbanucleosides: Synthesis and biological evaluation
- Roberto Romeo,
- Caterina Carnovale,
- Salvatore V. Giofrè,
- Maria A. Chiacchio,
- Adriana Garozzo,
- Emanuele Amata,
- Giovanni Romeo and
- Ugo Chiacchio
Beilstein J. Org. Chem. 2015, 11, 328–334, doi:10.3762/bjoc.11.38
Functionalized branched EDOT-terthiophene copolymer films by electropolymerization and post-polymerization “click”-reactions
- Miriam Goll,
- Adrian Ruff,
- Erna Muks,
- Felix Goerigk,
- Beatrice Omiecienski,
- Ines Ruff,
- Rafael C. González-Cano,
- Juan T. Lopez Navarrete,
- M. Carmen Ruiz Delgado and
- Sabine Ludwigs
Beilstein J. Org. Chem. 2015, 11, 335–347, doi:10.3762/bjoc.11.39
IR and electrochemical synthesis and characterization of thin films of PEDOT grown on platinum single crystal electrodes in [EMMIM]Tf2N ionic liquid
- Andrea P. Sandoval,
- Marco F. Suárez-Herrera and
- Juan M. Feliu
Beilstein J. Org. Chem. 2015, 11, 348–357, doi:10.3762/bjoc.11.40
Matsuda–Heck reaction with arenediazonium tosylates in water
- Ksenia V. Kutonova,
- Marina E. Trusova,
- Andrey V. Stankevich,
- Pavel S. Postnikov and
- Victor D. Filimonov
Beilstein J. Org. Chem. 2015, 11, 358–362, doi:10.3762/bjoc.11.41
Attempts to prepare an all-carbon indigoid system
- Şeref Yildizhan,
- Henning Hopf and
- Peter G. Jones
Beilstein J. Org. Chem. 2015, 11, 363–372, doi:10.3762/bjoc.11.42
Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s
- Natalia A. Danilkina,
- Petr S. Vlasov,
- Semen M. Vodianik,
- Andrey A. Kruchinin,
- Yuri G. Vlasov and
- Irina A. Balova
Beilstein J. Org. Chem. 2015, 11, 373–384, doi:10.3762/bjoc.11.43
The reactions of 2-ethoxymethylidene-3-oxo esters and their analogues with 5-aminotetrazole as a way to novel azaheterocycles
- Marina V. Goryaeva,
- Yanina V. Burgart,
- Marina A. Ezhikova,
- Mikhail I. Kodess and
- Viktor I. Saloutin
Beilstein J. Org. Chem. 2015, 11, 385–391, doi:10.3762/bjoc.11.44
Electrochemical oxidation of cholesterol
- Jacek W. Morzycki and
- Andrzej Sobkowiak
Beilstein J. Org. Chem. 2015, 11, 392–402, doi:10.3762/bjoc.11.45
Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF
- Erdal Ertas,
- İlknur Demirtas and
- Turan Ozturk
Beilstein J. Org. Chem. 2015, 11, 403–415, doi:10.3762/bjoc.11.46
Direct access to pyrido/pyrrolo[2,1-b]quinazolin-9(1H)-ones through silver-mediated intramolecular alkyne hydroamination reactions
- Hengshuai Wang,
- Shengchao Jiao,
- Kerong Chen,
- Xu Zhang,
- Linxiang Zhao,
- Dan Liu,
- Yu Zhou and
- Hong Liu
Beilstein J. Org. Chem. 2015, 11, 416–424, doi:10.3762/bjoc.11.47
Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides
- Zhongwei Liang,
- Song Xu,
- Wenyan Tian and
- Ronghua Zhang
Beilstein J. Org. Chem. 2015, 11, 425–430, doi:10.3762/bjoc.11.48
Ruthenium-catalyzed C–H activation of thioxanthones
- Danny Wagner and
- Stefan Bräse
Beilstein J. Org. Chem. 2015, 11, 431–436, doi:10.3762/bjoc.11.49
The preparation of new functionalized [2.2]paracyclophane derivatives with N-containing functional groups
- Henning Hopf,
- Swaminathan Vijay Narayanan and
- Peter G. Jones
Beilstein J. Org. Chem. 2015, 11, 437–445, doi:10.3762/bjoc.11.50
Chemoselective O-acylation of hydroxyamino acids and amino alcohols under acidic reaction conditions: History, scope and applications
- Tor E. Kristensen
Beilstein J. Org. Chem. 2015, 11, 446–468, doi:10.3762/bjoc.11.51
A procedure for the preparation and isolation of nucleoside-5’-diphosphates
- Heidi J. Korhonen,
- Hannah L. Bolt and
- David R. W. Hodgson
Beilstein J. Org. Chem. 2015, 11, 469–472, doi:10.3762/bjoc.11.52
Highly selective generation of vanillin by anodic degradation of lignin: a combined approach of electrochemistry and product isolation by adsorption
- Dominik Schmitt,
- Carolin Regenbrecht,
- Marius Hartmer,
- Florian Stecker and
- Siegfried R. Waldvogel
Beilstein J. Org. Chem. 2015, 11, 473–480, doi:10.3762/bjoc.11.53
Further exploration of the heterocyclic diversity accessible from the allylation chemistry of indigo
- Alireza Shakoori,
- John B. Bremner,
- Mohammed K. Abdel-Hamid,
- Anthony C. Willis,
- Rachada Haritakun and
- Paul A. Keller
Beilstein J. Org. Chem. 2015, 11, 481–492, doi:10.3762/bjoc.11.54
Sequence-specific RNA cleavage by PNA conjugates of the metal-free artificial ribonuclease tris(2-aminobenzimidazole)
- Friederike Danneberg,
- Alice Ghidini,
- Plamena Dogandzhiyski,
- Elisabeth Kalden,
- Roger Strömberg and
- Michael W. Göbel
Beilstein J. Org. Chem. 2015, 11, 493–498, doi:10.3762/bjoc.11.55
3-Glucosylated 5-amino-1,2,4-oxadiazoles: synthesis and evaluation as glycogen phosphorylase inhibitors
- Marion Donnier-Maréchal,
- David Goyard,
- Vincent Folliard,
- Tibor Docsa,
- Pal Gergely,
- Jean-Pierre Praly and
- Sébastien Vidal
Beilstein J. Org. Chem. 2015, 11, 499–503, doi:10.3762/bjoc.11.56
On the strong difference in reactivity of acyclic and cyclic diazodiketones with thioketones: experimental results and quantum-chemical interpretation
- Andrey S. Mereshchenko,
- Alexey V. Ivanov,
- Viktor I. Baranovskii,
- Grzegorz Mloston,
- Ludmila L. Rodina and
- Valerij A. Nikolaev
Beilstein J. Org. Chem. 2015, 11, 504–513, doi:10.3762/bjoc.11.57
Synthesis and surface grafting of a β-cyclodextrin dimer facilitating cooperative inclusion of 2,6-ANS
- Lars W. Städe,
- Thorbjørn T. Nielsen,
- Laurent Duroux,
- Reinhard Wimmer,
- Kyoko Shimizu and
- Kim L. Larsen
Beilstein J. Org. Chem. 2015, 11, 514–523, doi:10.3762/bjoc.11.58
Metal-free one-pot synthesis of 2-substituted and 2,3-disubstituted morpholines from aziridines
- Hongnan Sun,
- Binbin Huang,
- Run Lin,
- Chao Yang and
- Wujiong Xia
Beilstein J. Org. Chem. 2015, 11, 524–529, doi:10.3762/bjoc.11.59
Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams
- Katherine M. Byrd
Beilstein J. Org. Chem. 2015, 11, 530–562, doi:10.3762/bjoc.11.60
Fluoride-driven ‘turn on’ ESPT in the binding with a novel benzimidazole-based sensor
- Kai Liu,
- Xiaojun Zhao,
- Qingxiang Liu,
- Jianzhong Huo,
- Bolin Zhu and
- Shihua Diao
Beilstein J. Org. Chem. 2015, 11, 563–567, doi:10.3762/bjoc.11.61
Photocatalytic nucleophilic addition of alcohols to styrenes in Markovnikov and anti-Markovnikov orientation
- Martin Weiser,
- Sergej Hermann,
- Alexander Penner and
- Hans-Achim Wagenknecht
Beilstein J. Org. Chem. 2015, 11, 568–575, doi:10.3762/bjoc.11.62
Hetero-Diels–Alder reactions of hetaryl and aryl thioketones with acetylenic dienophiles
- Grzegorz Mlostoń,
- Paulina Grzelak,
- Maciej Mikina,
- Anthony Linden and
- Heinz Heimgartner
Beilstein J. Org. Chem. 2015, 11, 576–582, doi:10.3762/bjoc.11.63
Synthesis of 1,2-cis-2-C-branched aryl-C-glucosides via desulfurization of carbohydrate based hemithioacetals
- Henok H. Kinfe,
- Fanuel M. Mebrahtu,
- Mandlenkosi M. Manana,
- Kagiso Madumo and
- Mokela S. Sokamisa
Beilstein J. Org. Chem. 2015, 11, 583–588, doi:10.3762/bjoc.11.64
Potential of acylated peptides to target the influenza A virus
- Daniel Lauster,
- Damian Pawolski,
- Julian Storm,
- Kai Ludwig,
- Rudolf Volkmer,
- Henry Memczak,
- Andreas Herrmann and
- Sumati Bhatia
Beilstein J. Org. Chem. 2015, 11, 589–595, doi:10.3762/bjoc.11.65
Novel stereocontrolled syntheses of tashiromine and epitashiromine
- Loránd Kiss,
- Enikő Forró and
- Ferenc Fülöp
Beilstein J. Org. Chem. 2015, 11, 596–603, doi:10.3762/bjoc.11.66
