Supramolecular frameworks based on [60]fullerene hexakisadducts
- Andreas Kraft,
- Johannes Stangl,
- Ana-Maria Krause,
- Klaus Müller-Buschbaum and
- Florian Beuerle
Beilstein J. Org. Chem. 2017, 13, 1–9, doi:10.3762/bjoc.13.1
Synthesis of multi-lactose-appended β-cyclodextrin and its cholesterol-lowering effects in Niemann–Pick type C disease-like HepG2 cells
- Keiichi Motoyama,
- Rena Nishiyama,
- Yuki Maeda,
- Taishi Higashi,
- Yoichi Ishitsuka,
- Yuki Kondo,
- Tetsumi Irie,
- Takumi Era and
- Hidetoshi Arima
Beilstein J. Org. Chem. 2017, 13, 10–18, doi:10.3762/bjoc.13.2
Poly(ethylene glycol)s as grinding additives in the mechanochemical preparation of highly functionalized 3,5-disubstituted hydantoins
- Andrea Mascitti,
- Massimiliano Lupacchini,
- Ruben Guerra,
- Ilya Taydakov,
- Lucia Tonucci,
- Nicola d’Alessandro,
- Frederic Lamaty,
- Jean Martinez and
- Evelina Colacino
Beilstein J. Org. Chem. 2017, 13, 19–25, doi:10.3762/bjoc.13.3
Synthesis and evaluation of anti-oxidant and cytotoxic activities of novel 10-undecenoic acid methyl ester based lipoconjugates of phenolic acids
- Naganna Narra,
- Shiva Shanker Kaki,
- Rachapudi Badari Narayana Prasad,
- Sunil Misra,
- Koude Dhevendar,
- Venkateshwarlu Kontham and
- Padmaja V. Korlipara
Beilstein J. Org. Chem. 2017, 13, 26–32, doi:10.3762/bjoc.13.4
Diastereoselective anodic hetero- and homo-coupling of menthol-, 8-methylmenthol- and 8-phenylmenthol-2-alkylmalonates
- Matthias C. Letzel,
- Hans J. Schäfer and
- Roland Fröhlich
Beilstein J. Org. Chem. 2017, 13, 33–42, doi:10.3762/bjoc.13.5
Phosphated cyclodextrins as water-soluble chiral NMR solvating agents for cationic compounds
- Cira Mollings Puentes and
- Thomas J. Wenzel
Beilstein J. Org. Chem. 2017, 13, 43–53, doi:10.3762/bjoc.13.6
Synthesis of structurally diverse 3,4-dihydropyrimidin-2(1H)-ones via sequential Biginelli and Passerini reactions
- Andreas C. Boukis,
- Baptiste Monney and
- Michael A. R. Meier
Beilstein J. Org. Chem. 2017, 13, 54–62, doi:10.3762/bjoc.13.7
Strategies in asymmetric catalysis
- Tehshik P. Yoon
Beilstein J. Org. Chem. 2017, 13, 63–64, doi:10.3762/bjoc.13.8
Extrusion – back to the future: Using an established technique to reform automated chemical synthesis
- Deborah E. Crawford
Beilstein J. Org. Chem. 2017, 13, 65–75, doi:10.3762/bjoc.13.9
The synthesis of α-aryl-α-aminophosphonates and α-aryl-α-aminophosphine oxides by the microwave-assisted Pudovik reaction
- Erika Bálint,
- Ádám Tajti,
- Anna Ádám,
- István Csontos,
- Konstantin Karaghiosoff,
- Mátyás Czugler,
- Péter Ábrányi-Balogh and
- György Keglevich
Beilstein J. Org. Chem. 2017, 13, 76–86, doi:10.3762/bjoc.13.10
Nucleophilic displacement reactions of 5′-derivatised nucleosides in a vibration ball mill
- Olga Eguaogie,
- Patrick F. Conlon,
- Francesco Ravalico,
- Jamie S. T. Sweet,
- Thomas B. Elder,
- Louis P. Conway,
- Marc E. Lennon,
- David R. W. Hodgson and
- Joseph S. Vyle
Beilstein J. Org. Chem. 2017, 13, 87–92, doi:10.3762/bjoc.13.11
Silyl-protective groups influencing the reactivity and selectivity in glycosylations
- Mikael Bols and
- Christian Marcus Pedersen
Beilstein J. Org. Chem. 2017, 13, 93–105, doi:10.3762/bjoc.13.12
Solution-phase automated synthesis of an α-amino aldehyde as a versatile intermediate
- Hisashi Masui,
- Sae Yosugi,
- Shinichiro Fuse and
- Takashi Takahashi
Beilstein J. Org. Chem. 2017, 13, 106–110, doi:10.3762/bjoc.13.13
3D printed fluidics with embedded analytic functionality for automated reaction optimisation
- Andrew J. Capel,
- Andrew Wright,
- Matthew J. Harding,
- George W. Weaver,
- Yuqi Li,
- Russell A. Harris,
- Steve Edmondson,
- Ruth D. Goodridge and
- Steven D. R. Christie
Beilstein J. Org. Chem. 2017, 13, 111–119, doi:10.3762/bjoc.13.14
Diels–Alder reactions of myrcene using intensified continuous-flow reactors
- Christian H. Hornung,
- Miguel Á. Álvarez-Diéguez,
- Thomas M. Kohl and
- John Tsanaktsidis
Beilstein J. Org. Chem. 2017, 13, 120–126, doi:10.3762/bjoc.13.15
A postsynthetically 2’-“clickable” uridine with arabino configuration and its application for fluorescent labeling and imaging of DNA
- Heidi-Kristin Walter,
- Bettina Olshausen,
- Ute Schepers and
- Hans-Achim Wagenknecht
Beilstein J. Org. Chem. 2017, 13, 127–137, doi:10.3762/bjoc.13.16
A new class of organogelators based on triphenylmethyl derivatives of primary alcohols: hydrophobic interactions alone can mediate gelation
- Wangkhem P. Singh and
- Rajkumar S. Singh
Beilstein J. Org. Chem. 2017, 13, 138–149, doi:10.3762/bjoc.13.17
Self-optimisation and model-based design of experiments for developing a C–H activation flow process
- Alexander Echtermeyer,
- Yehia Amar,
- Jacek Zakrzewski and
- Alexei Lapkin
Beilstein J. Org. Chem. 2017, 13, 150–163, doi:10.3762/bjoc.13.18
Total synthesis of a Streptococcus pneumoniae serotype 12F CPS repeating unit hexasaccharide
- Peter H. Seeberger,
- Claney L. Pereira and
- Subramanian Govindan
Beilstein J. Org. Chem. 2017, 13, 164–173, doi:10.3762/bjoc.13.19
A novel method for heterocyclic amide–thioamide transformations
- Walid Fathalla,
- Ibrahim A. I. Ali and
- Pavel Pazdera
Beilstein J. Org. Chem. 2017, 13, 174–181, doi:10.3762/bjoc.13.20
Dynamics and interactions of ibuprofen in cyclodextrin nanosponges by solid-state NMR spectroscopy
- Monica Ferro,
- Franca Castiglione,
- Nadia Pastori,
- Carlo Punta,
- Lucio Melone,
- Walter Panzeri,
- Barbara Rossi,
- Francesco Trotta and
- Andrea Mele
Beilstein J. Org. Chem. 2017, 13, 182–194, doi:10.3762/bjoc.13.21
Efficient access to β-vinylporphyrin derivatives via palladium cross coupling of β-bromoporphyrins with N-tosylhydrazones
- Vinicius R. Campos,
- Ana T. P. C. Gomes,
- Anna C. Cunha,
- Maria da Graça P. M. S. Neves,
- Vitor F. Ferreira and
- José A. S. Cavaleiro
Beilstein J. Org. Chem. 2017, 13, 195–202, doi:10.3762/bjoc.13.22
Interactions between photoacidic 3-hydroxynaphtho[1,2-b]quinolizinium and cucurbit[7]uril: Influence on acidity in the ground and excited state
- Jonas Becher,
- Daria V. Berdnikova,
- Darinka Dzubiel,
- Heiko Ihmels and
- Phil M. Pithan
Beilstein J. Org. Chem. 2017, 13, 203–212, doi:10.3762/bjoc.13.23
Highly bulky and stable geometry-constrained iminopyridines: Synthesis, structure and application in Pd-catalyzed Suzuki coupling of aryl chlorides
- Yi Lai,
- Zhijian Zong,
- Yujie Tang,
- Weimin Mo,
- Nan Sun,
- Baoxiang Hu,
- Zhenlu Shen,
- Liqun Jin,
- Wen-hua Sun and
- Xinquan Hu
Beilstein J. Org. Chem. 2017, 13, 213–221, doi:10.3762/bjoc.13.24
Spectral and DFT studies of anion bound organic receptors: Time dependent studies and logic gate applications
- Srikala Pangannaya,
- Neethu Padinchare Purayil,
- Shweta Dabhi,
- Venu Mankad,
- Prafulla K. Jha,
- Satyam Shinde and
- Darshak R. Trivedi
Beilstein J. Org. Chem. 2017, 13, 222–238, doi:10.3762/bjoc.13.25
Continuous-flow synthesis of highly functionalized imidazo-oxadiazoles facilitated by microfluidic extraction
- Ananda Herath and
- Nicholas D. P. Cosford
Beilstein J. Org. Chem. 2017, 13, 239–246, doi:10.3762/bjoc.13.26
Versatile synthesis of the signaling peptide glorin
- Robert Barnett,
- Daniel Raszkowski,
- Thomas Winckler and
- Pierre Stallforth
Beilstein J. Org. Chem. 2017, 13, 247–250, doi:10.3762/bjoc.13.27
Revaluation of biomass-derived furfuryl alcohol derivatives for the synthesis of carbocyclic nucleoside phosphonate analogues
- Bemba Sidi Mohamed,
- Christian Périgaud and
- Christophe Mathé
Beilstein J. Org. Chem. 2017, 13, 251–256, doi:10.3762/bjoc.13.28
Regiochemistry of cyclocondensation reactions in the synthesis of polyazaheterocycles
- Patrick T. Campos,
- Leticia V. Rodrigues,
- Andrei L. Belladona,
- Caroline R. Bender,
- Juliana S. Bitencurt,
- Fernanda A. Rosa,
- Davi F. Back,
- Helio G. Bonacorso,
- Nilo Zanatta,
- Clarissa P. Frizzo and
- Marcos A. P. Martins
Beilstein J. Org. Chem. 2017, 13, 257–266, doi:10.3762/bjoc.13.29
The reductive decyanation reaction: an overview and recent developments
- Jean-Marc R. Mattalia
Beilstein J. Org. Chem. 2017, 13, 267–284, doi:10.3762/bjoc.13.30
NMR reaction monitoring in flow synthesis
- M. Victoria Gomez and
- Antonio de la Hoz
Beilstein J. Org. Chem. 2017, 13, 285–300, doi:10.3762/bjoc.13.31
