Sulfation and amidinohydrolysis in the biosynthesis of giant linear polyenes
- Hui Hong,
- Markiyan Samborskyy,
- Katsiaryna Usachova,
- Katharina Schnatz and
- Peter F. Leadlay
Beilstein J. Org. Chem. 2017, 13, 2408–2415, doi:10.3762/bjoc.13.238
Exploring mechanochemistry to turn organic bio-relevant molecules into metal-organic frameworks: a short review
- Vânia André,
- Sílvia Quaresma,
- João Luís Ferreira da Silva and
- M. Teresa Duarte
Beilstein J. Org. Chem. 2017, 13, 2416–2427, doi:10.3762/bjoc.13.239
Asymmetric synthesis of propargylamines as amino acid surrogates in peptidomimetics
- Matthias Wünsch,
- David Schröder,
- Tanja Fröhr,
- Lisa Teichmann,
- Sebastian Hedwig,
- Nils Janson,
- Clara Belu,
- Jasmin Simon,
- Shari Heidemeyer,
- Philipp Holtkamp,
- Jens Rudlof,
- Lennard Klemme,
- Alessa Hinzmann,
- Beate Neumann,
- Hans-Georg Stammler and
- Norbert Sewald
Beilstein J. Org. Chem. 2017, 13, 2428–2441, doi:10.3762/bjoc.13.240
Hydrolysis, polarity, and conformational impact of C-terminal partially fluorinated ethyl esters in peptide models
- Vladimir Kubyshkin and
- Nediljko Budisa
Beilstein J. Org. Chem. 2017, 13, 2442–2457, doi:10.3762/bjoc.13.241
Herpetopanone, a diterpene from Herpetosiphon aurantiacus discovered by isotope labeling
- Xinli Pan,
- Nicole Domin,
- Sebastian Schieferdecker,
- Hirokazu Kage,
- Martin Roth and
- Markus Nett
Beilstein J. Org. Chem. 2017, 13, 2458–2465, doi:10.3762/bjoc.13.242
Synthesis of naturally-derived macromolecules through simplified electrochemically mediated ATRP
- Paweł Chmielarz,
- Tomasz Pacześniak,
- Katarzyna Rydel-Ciszek,
- Izabela Zaborniak,
- Paulina Biedka and
- Andrzej Sobkowiak
Beilstein J. Org. Chem. 2017, 13, 2466–2472, doi:10.3762/bjoc.13.243
Diastereoselective Mannich reactions of pseudo-C2-symmetric glutarimide with activated imines
- Tatsuya Ishikawa,
- Tomoko Kawasaki-Takasuka,
- Toshio Kubota and
- Takashi Yamazaki
Beilstein J. Org. Chem. 2017, 13, 2473–2477, doi:10.3762/bjoc.13.244
A permutation approach to the assignment of the configuration to diastereomeric tetrads by comparison of experimental and ab initio calculated differences in NMR data
- Przemysław J. Boratyński
Beilstein J. Org. Chem. 2017, 13, 2478–2485, doi:10.3762/bjoc.13.245
Syntheses, structures, and stabilities of aliphatic and aromatic fluorous iodine(I) and iodine(III) compounds: the role of iodine Lewis basicity
- Tathagata Mukherjee,
- Soumik Biswas,
- Andreas Ehnbom,
- Subrata K. Ghosh,
- Ibrahim El-Zoghbi,
- Nattamai Bhuvanesh,
- Hassan S. Bazzi and
- John A. Gladysz
Beilstein J. Org. Chem. 2017, 13, 2486–2501, doi:10.3762/bjoc.13.246
One-pot three-component route for the synthesis of S-trifluoromethyl dithiocarbamates using Togni’s reagent
- Azim Ziyaei Halimehjani,
- Martin Dračínský and
- Petr Beier
Beilstein J. Org. Chem. 2017, 13, 2502–2508, doi:10.3762/bjoc.13.247
Synthesis and supramolecular properties of regioisomers of mononaphthylallyl derivatives of γ-cyclodextrin
- Markéta Bláhová,
- Sergey K. Filippov,
- Lubomír Kováčik,
- Jiří Horský,
- Simona Hybelbauerová,
- Zdenka Syrová,
- Tomáš Křížek and
- Jindřich Jindřich
Beilstein J. Org. Chem. 2017, 13, 2509–2520, doi:10.3762/bjoc.13.248
Pyrene–nucleobase conjugates: synthesis, oligonucleotide binding and confocal bioimaging studies
- Artur Jabłoński,
- Yannic Fritz,
- Hans-Achim Wagenknecht,
- Rafał Czerwieniec,
- Tytus Bernaś,
- Damian Trzybiński,
- Krzysztof Woźniak and
- Konrad Kowalski
Beilstein J. Org. Chem. 2017, 13, 2521–2534, doi:10.3762/bjoc.13.249
15N-Labelling and structure determination of adamantylated azolo-azines in solution
- Sergey L. Deev,
- Alexander S. Paramonov,
- Tatyana S. Shestakova,
- Igor A. Khalymbadzha,
- Oleg N. Chupakhin,
- Julia O. Subbotina,
- Oleg S. Eltsov,
- Pavel A. Slepukhin,
- Vladimir L. Rusinov,
- Alexander S. Arseniev and
- Zakhar O. Shenkarev
Beilstein J. Org. Chem. 2017, 13, 2535–2548, doi:10.3762/bjoc.13.250
A concise flow synthesis of indole-3-carboxylic ester and its derivatisation to an auxin mimic
- Marcus Baumann,
- Ian R. Baxendale and
- Fabien Deplante
Beilstein J. Org. Chem. 2017, 13, 2549–2560, doi:10.3762/bjoc.13.251
A novel synthetic approach to hydroimidazo[1,5-b]pyridazines by the recyclization of itaconimides and HPLC–HRMS monitoring of the reaction pathway
- Dmitry Yu. Vandyshev,
- Khidmet S. Shikhaliev,
- Andrey Yu. Potapov,
- Michael Yu. Krysin,
- Fedor I. Zubkov and
- Lyudmila V. Sapronova
Beilstein J. Org. Chem. 2017, 13, 2561–2568, doi:10.3762/bjoc.13.252
Rh(II)-mediated domino [4 + 1]-annulation of α-cyanothioacetamides using diazoesters: A new entry for the synthesis of multisubstituted thiophenes
- Jury J. Medvedev,
- Ilya V. Efimov,
- Yuri M. Shafran,
- Vitaliy V. Suslonov,
- Vasiliy A. Bakulev and
- Valerij A. Nikolaev
Beilstein J. Org. Chem. 2017, 13, 2569–2576, doi:10.3762/bjoc.13.253
Synthesis of 1,3-cis-disubstituted sterically encumbered imidazolidinone organocatalysts
- Jan Wallbaum and
- Daniel B. Werz
Beilstein J. Org. Chem. 2017, 13, 2577–2583, doi:10.3762/bjoc.13.254
What contributes to an effective mannose recognition domain?
- Christoph P. Sager,
- Deniz Eriş,
- Martin Smieško,
- Rachel Hevey and
- Beat Ernst
Beilstein J. Org. Chem. 2017, 13, 2584–2595, doi:10.3762/bjoc.13.255
Consecutive hydrazino-Ugi-azide reactions: synthesis of acylhydrazines bearing 1,5-disubstituted tetrazoles
- Angélica de Fátima S. Barreto,
- Veronica Alves dos Santos and
- Carlos Kleber Z. Andrade
Beilstein J. Org. Chem. 2017, 13, 2596–2602, doi:10.3762/bjoc.13.256
A semisynthesis of 3'-O-ethyl-5,6-dihydrospinosyn J based on the spinosyn A aglycone
- Kai Zhang,
- Shenglan Liu,
- Anjun Liu,
- Hongxin Chai,
- Jiarong Li and
- Lamusi A
Beilstein J. Org. Chem. 2017, 13, 2603–2609, doi:10.3762/bjoc.13.257
Palladium-catalyzed Heck-type reaction of secondary trifluoromethylated alkyl bromides
- Tao Fan,
- Wei-Dong Meng and
- Xingang Zhang
Beilstein J. Org. Chem. 2017, 13, 2610–2616, doi:10.3762/bjoc.13.258
Regioselective decarboxylative addition of malonic acid and its mono(thio)esters to 4-trifluoromethylpyrimidin-2(1H)-ones
- Sergii V. Melnykov,
- Andrii S. Pataman,
- Yurii V. Dmytriv,
- Svitlana V. Shishkina,
- Mykhailo V. Vovk and
- Volodymyr A. Sukach
Beilstein J. Org. Chem. 2017, 13, 2617–2625, doi:10.3762/bjoc.13.259
Electrophilic trifluoromethylselenolation of terminal alkynes with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate
- Clément Ghiazza,
- Anis Tlili and
- Thierry Billard
Beilstein J. Org. Chem. 2017, 13, 2626–2630, doi:10.3762/bjoc.13.260
An efficient synthesis of 1,6-anhydro-N-acetylmuramic acid from N-acetylglucosamine
- Matthew B. Calvert,
- Christoph Mayer and
- Alexander Titz
Beilstein J. Org. Chem. 2017, 13, 2631–2636, doi:10.3762/bjoc.13.261
Recent progress in the racemic and enantioselective synthesis of monofluoroalkene-based dipeptide isosteres
- Myriam Drouin and
- Jean-François Paquin
Beilstein J. Org. Chem. 2017, 13, 2637–2658, doi:10.3762/bjoc.13.262
Preparation and isolation of isobenzofuran
- Morten K. Peters and
- Rainer Herges
Beilstein J. Org. Chem. 2017, 13, 2659–2662, doi:10.3762/bjoc.13.263
A Brønsted base-promoted diastereoselective dimerization of azlactones
- Danielle L. J. Pinheiro,
- Gabriel M. F. Batista,
- Pedro P. de Castro,
- Leonã S. Flores,
- Gustavo F. S. Andrade and
- Giovanni W. Amarante
Beilstein J. Org. Chem. 2017, 13, 2663–2670, doi:10.3762/bjoc.13.264
![[Graphic 5]](/bjoc/content/inline/1860-5397-13-264-i10.svg?max-width=637&scale=1.18182)
vs time for the dimerization of azlactone 1a.
Metal-mediated base pairs in parallel-stranded DNA
- Jens Müller
Beilstein J. Org. Chem. 2017, 13, 2671–2681, doi:10.3762/bjoc.13.265
Ring-size-selective construction of fluorine-containing carbocycles via intramolecular iodoarylation of 1,1-difluoro-1-alkenes
- Takeshi Fujita,
- Ryo Kinoshita,
- Tsuyoshi Takanohashi,
- Naoto Suzuki and
- Junji Ichikawa
Beilstein J. Org. Chem. 2017, 13, 2682–2689, doi:10.3762/bjoc.13.266
Development of a fluorogenic small substrate for dipeptidyl peptidase-4
- Futa Ogawa,
- Masanori Takeda,
- Kanae Miyanaga,
- Keita Tani,
- Ryuji Yamazawa,
- Kiyoshi Ito,
- Atsushi Tarui,
- Kazuyuki Sato and
- Masaaki Omote
Beilstein J. Org. Chem. 2017, 13, 2690–2697, doi:10.3762/bjoc.13.267
Binding abilities of a chiral calix[4]resorcinarene: a polarimetric investigation on a complex case of study
- Marco Russo and
- Paolo Lo Meo
Beilstein J. Org. Chem. 2017, 13, 2698–2709, doi:10.3762/bjoc.13.268
