Base-promoted isomerization of CF3-containing allylic alcohols to the corresponding saturated ketones under metal-free conditions
- Yoko Hamada,
- Tomoko Kawasaki-Takasuka and
- Takashi Yamazaki
Beilstein J. Org. Chem. 2017, 13, 1507–1512, doi:10.3762/bjoc.13.149
Phenylsilane as an effective desulfinylation reagent
- Wanda H. Midura,
- Aneta Rzewnicka and
- Jerzy A. Krysiak
Beilstein J. Org. Chem. 2017, 13, 1513–1517, doi:10.3762/bjoc.13.150
Bifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides
- Ryota Miyaji,
- Yuuki Wada,
- Akira Matsumoto,
- Keisuke Asano and
- Seijiro Matsubara
Beilstein J. Org. Chem. 2017, 13, 1518–1523, doi:10.3762/bjoc.13.151
Direct catalytic arylation of heteroarenes with meso-bromophenyl-substituted porphyrins
- Alexei N. Kiselev,
- Olga K. Grigorova,
- Alexei D. Averin,
- Sergei A. Syrbu,
- Oskar I. Koifman and
- Irina P. Beletskaya
Beilstein J. Org. Chem. 2017, 13, 1524–1532, doi:10.3762/bjoc.13.152
Effect of uridine protecting groups on the diastereoselectivity of uridine-derived aldehyde 5’-alkynylation
- Raja Ben Othman,
- Mickaël J. Fer,
- Laurent Le Corre,
- Sandrine Calvet-Vitale and
- Christine Gravier-Pelletier
Beilstein J. Org. Chem. 2017, 13, 1533–1541, doi:10.3762/bjoc.13.153
Synthesis and metal binding properties of N-alkylcarboxyspiropyrans
- Alexis Perry and
- Christina J. Kousseff
Beilstein J. Org. Chem. 2017, 13, 1542–1550, doi:10.3762/bjoc.13.154
Chemical systems, chemical contiguity and the emergence of life
- Terrence P. Kee and
- Pierre-Alain Monnard
Beilstein J. Org. Chem. 2017, 13, 1551–1563, doi:10.3762/bjoc.13.155
A novel approach to oxoisoaporphine alkaloids via regioselective metalation of alkoxy isoquinolines
- Benedikt C. Melzer and
- Franz Bracher
Beilstein J. Org. Chem. 2017, 13, 1564–1571, doi:10.3762/bjoc.13.156
Molecular recognition of N-acetyltryptophan enantiomers by β-cyclodextrin
- Spyros D. Chatziefthimiou,
- Mario Inclán,
- Petros Giastas,
- Athanasios Papakyriakou,
- Konstantina Yannakopoulou and
- Irene M. Mavridis
Beilstein J. Org. Chem. 2017, 13, 1572–1582, doi:10.3762/bjoc.13.157
New electroactive asymmetrical chalcones and therefrom derived 2-amino- / 2-(1H-pyrrol-1-yl)pyrimidines, containing an N-[ω-(4-methoxyphenoxy)alkyl]carbazole fragment: synthesis, optical and electrochemical properties
- Daria G. Selivanova,
- Alexei A. Gorbunov,
- Olga A. Mayorova,
- Alexander N. Vasyanin,
- Igor V. Lunegov,
- Elena V. Shklyaeva and
- Georgii G. Abashev
Beilstein J. Org. Chem. 2017, 13, 1583–1595, doi:10.3762/bjoc.13.158
The chemistry and biology of mycolactones
- Matthias Gehringer and
- Karl-Heinz Altmann
Beilstein J. Org. Chem. 2017, 13, 1596–1660, doi:10.3762/bjoc.13.159
Encaging palladium(0) in layered double hydroxide: A sustainable catalyst for solvent-free and ligand-free Heck reaction in a ball mill
- Wei Shi,
- Jingbo Yu,
- Zhijiang Jiang,
- Qiaoling Shao and
- Weike Su
Beilstein J. Org. Chem. 2017, 13, 1661–1668, doi:10.3762/bjoc.13.160
Correction: Dynamic behavior of rearranging carbocations – implications for terpene biosynthesis
- Stephanie R. Hare and
- Dean J. Tantillo
Beilstein J. Org. Chem. 2017, 13, 1669–1669, doi:10.3762/bjoc.13.161
Oxidative dehydrogenation of C–C and C–N bonds: A convenient approach to access diverse (dihydro)heteroaromatic compounds
- Santanu Hati,
- Ulrike Holzgrabe and
- Subhabrata Sen
Beilstein J. Org. Chem. 2017, 13, 1670–1692, doi:10.3762/bjoc.13.162
Block copolymers from ionic liquids for the preparation of thin carbonaceous shells
- Sadaf Hanif,
- Bernd Oschmann,
- Dmitri Spetter,
- Muhammad Nawaz Tahir,
- Wolfgang Tremel and
- Rudolf Zentel
Beilstein J. Org. Chem. 2017, 13, 1693–1701, doi:10.3762/bjoc.13.163
A recursive microfluidic platform to explore the emergence of chemical evolution
- David Doran,
- Marc Rodriguez-Garcia,
- Rebecca Turk-MacLeod,
- Geoffrey J. T. Cooper and
- Leroy Cronin
Beilstein J. Org. Chem. 2017, 13, 1702–1709, doi:10.3762/bjoc.13.164
Theoretical simulation of the infrared signature of mechanically stressed polymer solids
- Matthew S. Sammon,
- Milan Ončák and
- Martin K. Beyer
Beilstein J. Org. Chem. 2017, 13, 1710–1716, doi:10.3762/bjoc.13.165
An effective Pd nanocatalyst in aqueous media: stilbene synthesis by Mizoroki–Heck coupling reaction under microwave irradiation
- Carolina S. García,
- Paula M. Uberman and
- Sandra E. Martín
Beilstein J. Org. Chem. 2017, 13, 1717–1727, doi:10.3762/bjoc.13.166
Mechanochemical enzymatic resolution of N-benzylated-β3-amino esters
- Mario Pérez-Venegas,
- Gloria Reyes-Rangel,
- Adrián Neri,
- Jaime Escalante and
- Eusebio Juaristi
Beilstein J. Org. Chem. 2017, 13, 1728–1734, doi:10.3762/bjoc.13.167
An efficient Pd–NHC catalyst system in situ generated from Na2PdCl4 and PEG-functionalized imidazolium salts for Mizoroki–Heck reactions in water
- Nan Sun,
- Meng Chen,
- Liqun Jin,
- Wei Zhao,
- Baoxiang Hu,
- Zhenlu Shen and
- Xinquan Hu
Beilstein J. Org. Chem. 2017, 13, 1735–1744, doi:10.3762/bjoc.13.168
Mechanochemical N-alkylation of imides
- Anamarija Briš,
- Mateja Đud and
- Davor Margetić
Beilstein J. Org. Chem. 2017, 13, 1745–1752, doi:10.3762/bjoc.13.169
Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles
- Johannes Schörgenhumer,
- Maximilian Tiffner and
- Mario Waser
Beilstein J. Org. Chem. 2017, 13, 1753–1769, doi:10.3762/bjoc.13.170
18-Hydroxydolabella-3,7-diene synthase – a diterpene synthase from Chitinophaga pinensis
- Jeroen S. Dickschat,
- Jan Rinkel,
- Patrick Rabe,
- Arman Beyraghdar Kashkooli and
- Harro J. Bouwmeester
Beilstein J. Org. Chem. 2017, 13, 1770–1780, doi:10.3762/bjoc.13.171
Conformational impact of structural modifications in 2-fluorocyclohexanone
- Francisco A. Martins,
- Josué M. Silla and
- Matheus P. Freitas
Beilstein J. Org. Chem. 2017, 13, 1781–1787, doi:10.3762/bjoc.13.172
Selective enzymatic esterification of lignin model compounds in the ball mill
- Ulla Weißbach,
- Saumya Dabral,
- Laure Konnert,
- Carsten Bolm and
- José G. Hernández
Beilstein J. Org. Chem. 2017, 13, 1788–1795, doi:10.3762/bjoc.13.173
Ni nanoparticles on RGO as reusable heterogeneous catalyst: effect of Ni particle size and intermediate composite structures in C–S cross-coupling reaction
- Debasish Sengupta,
- Koushik Bhowmik,
- Goutam De and
- Basudeb Basu
Beilstein J. Org. Chem. 2017, 13, 1796–1806, doi:10.3762/bjoc.13.174
