Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
- Sambasivarao Kotha,
- Ongolu Ravikumar and
- Jadab Majhi
Beilstein J. Org. Chem. 2015, 11, 1503–1508, doi:10.3762/bjoc.11.163
The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine
- Piotr Roszkowski,
- Jan. K. Maurin and
- Zbigniew Czarnocki
Beilstein J. Org. Chem. 2015, 11, 1509–1513, doi:10.3762/bjoc.11.164
Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps
- Sambasivarao Kotha,
- Ajay Kumar Chinnam and
- Mukesh E. Shirbhate
Beilstein J. Org. Chem. 2015, 11, 1514–1519, doi:10.3762/bjoc.11.165
Ruthenium indenylidene “1st generation” olefin metathesis catalysts containing triisopropyl phosphite
- Stefano Guidone,
- Fady Nahra,
- Alexandra M. Z. Slawin and
- Catherine S. J. Cazin
Beilstein J. Org. Chem. 2015, 11, 1520–1527, doi:10.3762/bjoc.11.166
Tetrathiafulvalene chemistry
- Peter J. Skabara and
- Marc Sallé
Beilstein J. Org. Chem. 2015, 11, 1528–1529, doi:10.3762/bjoc.11.167
Qualitative evaluation of regioselectivity in the formation of di- and tri-6-O-tritylates of α-cyclodextrin
- Keisuke Yoshikiyo,
- Yoshihisa Matsui and
- Tatsuyuki Yamamoto
Beilstein J. Org. Chem. 2015, 11, 1530–1540, doi:10.3762/bjoc.11.168
Latent ruthenium–indenylidene catalysts bearing a N-heterocyclic carbene and a bidentate picolinate ligand
- Thibault E. Schmid,
- Florian Modicom,
- Adrien Dumas,
- Etienne Borré,
- Loic Toupet,
- Olivier Baslé and
- Marc Mauduit
Beilstein J. Org. Chem. 2015, 11, 1541–1546, doi:10.3762/bjoc.11.169
Towards inhibitors of glycosyltransferases: A novel approach to the synthesis of 3-acetamido-3-deoxy-D-psicofuranose derivatives
- Maroš Bella,
- Miroslav Koóš and
- Chun-Hung Lin
Beilstein J. Org. Chem. 2015, 11, 1547–1552, doi:10.3762/bjoc.11.170
Preparation of a disulfide-linked precipitative soluble support for solution-phase synthesis of trimeric oligodeoxyribonucleotide 3´-(2-chlorophenylphosphate) building blocks
- Amit M. Jabgunde,
- Alejandro Gimenez Molina,
- Pasi Virta and
- Harri Lönnberg
Beilstein J. Org. Chem. 2015, 11, 1553–1560, doi:10.3762/bjoc.11.171
Synthesis of racemic and chiral BEDT-TTF derivatives possessing hydroxy groups and their achiral and chiral charge transfer complexes
- Sara J. Krivickas,
- Chiho Hashimoto,
- Junya Yoshida,
- Akira Ueda,
- Kazuyuki Takahashi,
- John D. Wallis and
- Hatsumi Mori
Beilstein J. Org. Chem. 2015, 11, 1561–1569, doi:10.3762/bjoc.11.172
Preparative semiconductor photoredox catalysis: An emerging theme in organic synthesis
- David W. Manley and
- John C. Walton
Beilstein J. Org. Chem. 2015, 11, 1570–1582, doi:10.3762/bjoc.11.173
Dicarboxylic esters: Useful tools for the biocatalyzed synthesis of hybrid compounds and polymers
- Ivan Bassanini,
- Karl Hult and
- Sergio Riva
Beilstein J. Org. Chem. 2015, 11, 1583–1595, doi:10.3762/bjoc.11.174
Star-shaped tetrathiafulvalene oligomers towards the construction of conducting supramolecular assembly
- Masahiko Iyoda and
- Masashi Hasegawa
Beilstein J. Org. Chem. 2015, 11, 1596–1613, doi:10.3762/bjoc.11.175
Robust bifunctional aluminium–salen catalysts for the preparation of cyclic carbonates from carbon dioxide and epoxides
- Yuri A. Rulev,
- Zalina Gugkaeva,
- Victor I. Maleev,
- Michael North and
- Yuri N. Belokon
Beilstein J. Org. Chem. 2015, 11, 1614–1623, doi:10.3762/bjoc.11.176
The facile construction of the phthalazin-1(2H)-one scaffold via copper-mediated C–H(sp2)/C–H(sp) coupling under mild conditions
- Wei Zhu,
- Bao Wang,
- Shengbin Zhou and
- Hong Liu
Beilstein J. Org. Chem. 2015, 11, 1624–1631, doi:10.3762/bjoc.11.177
Grubbs–Hoveyda type catalysts bearing a dicationic N-heterocyclic carbene for biphasic olefin metathesis reactions in ionic liquids
- Maximilian Koy,
- Hagen J. Altmann,
- Benjamin Autenrieth,
- Wolfgang Frey and
- Michael R. Buchmeiser
Beilstein J. Org. Chem. 2015, 11, 1632–1638, doi:10.3762/bjoc.11.178
Progress in metathesis chemistry II
- Karol Grela
Beilstein J. Org. Chem. 2015, 11, 1639–1640, doi:10.3762/bjoc.11.179
Reaction of allene esters with Selectfluor/TMSX (X = I, Br, Cl) and Selectfluor/NH4SCN: Competing oxidative/electrophilic dihalogenation and nucleophilic/conjugate addition
- A. Srinivas Reddy and
- Kenneth K. Laali
Beilstein J. Org. Chem. 2015, 11, 1641–1648, doi:10.3762/bjoc.11.180
Fates of imine intermediates in radical cyclizations of N-sulfonylindoles and ene-sulfonamides
- Hanmo Zhang,
- E. Ben Hay,
- Stephen J. Geib and
- Dennis P. Curran
Beilstein J. Org. Chem. 2015, 11, 1649–1655, doi:10.3762/bjoc.11.181
A facile synthetic route to benzimidazolium salts bearing bulky aromatic N-substituents
- Gabriele Grieco,
- Olivier Blacque and
- Heinz Berke
Beilstein J. Org. Chem. 2015, 11, 1656–1666, doi:10.3762/bjoc.11.182
Pyridinoacridine alkaloids of marine origin: NMR and MS spectral data, synthesis, biosynthesis and biological activity
- Louis P. Sandjo,
- Victor Kuete and
- Maique W. Biavatti
Beilstein J. Org. Chem. 2015, 11, 1667–1699, doi:10.3762/bjoc.11.183
SmI2-mediated dimerization of indolylbutenones and synthesis of the myxobacterial natural product indiacen B
- Nils Marsch,
- Peter G. Jones and
- Thomas Lindel
Beilstein J. Org. Chem. 2015, 11, 1700–1706, doi:10.3762/bjoc.11.184
An efficient synthesis of N-substituted 3-nitrothiophen-2-amines
- Sundaravel Vivek Kumar,
- Shanmugam Muthusubramanian,
- J. Carlos Menéndez and
- Subbu Perumal
Beilstein J. Org. Chem. 2015, 11, 1707–1712, doi:10.3762/bjoc.11.185
Active site diversification of P450cam with indole generates catalysts for benzylic oxidation reactions
- Paul P. Kelly,
- Anja Eichler,
- Susanne Herter,
- David C. Kranz,
- Nicholas J. Turner and
- Sabine L. Flitsch
Beilstein J. Org. Chem. 2015, 11, 1713–1720, doi:10.3762/bjoc.11.186
Dimethylamine as the key intermediate generated in situ from dimethylformamide (DMF) for the synthesis of thioamides
- Weibing Liu,
- Cui Chen and
- Hailing Liu
Beilstein J. Org. Chem. 2015, 11, 1721–1726, doi:10.3762/bjoc.11.187
Design and synthesis of propellane derivatives and oxa-bowls via ring-rearrangement metathesis as a key step
- Sambasivarao Kotha and
- Rama Gunta
Beilstein J. Org. Chem. 2015, 11, 1727–1731, doi:10.3762/bjoc.11.188
Fe(II)/Et3N-Relay-catalyzed domino reaction of isoxazoles with imidazolium salts in the synthesis of methyl 4-imidazolylpyrrole-2-carboxylates, its ylide and betaine derivatives
- Ekaterina E. Galenko,
- Olesya A. Tomashenko,
- Alexander F. Khlebnikov,
- Mikhail S. Novikov and
- Taras L. Panikorovskii
Beilstein J. Org. Chem. 2015, 11, 1732–1740, doi:10.3762/bjoc.11.189
Engineering Pichia pastoris for improved NADH regeneration: A novel chassis strain for whole-cell catalysis
- Martina Geier,
- Christoph Brandner,
- Gernot A. Strohmeier,
- Mélanie Hall,
- Franz S. Hartner and
- Anton Glieder
Beilstein J. Org. Chem. 2015, 11, 1741–1748, doi:10.3762/bjoc.11.190
Polythiophene and oligothiophene systems modified by TTF electroactive units for organic electronics
- Alexander L. Kanibolotsky,
- Neil J. Findlay and
- Peter J. Skabara
Beilstein J. Org. Chem. 2015, 11, 1749–1766, doi:10.3762/bjoc.11.191
A comprehensive study of olefin metathesis catalyzed by Ru-based catalysts
- Albert Poater and
- Luigi Cavallo
Beilstein J. Org. Chem. 2015, 11, 1767–1780, doi:10.3762/bjoc.11.192
The simple production of nonsymmetric quaterpyridines through Kröhnke pyridine synthesis
- Isabelle Sasaki,
- Jean-Claude Daran and
- Gérard Commenges
Beilstein J. Org. Chem. 2015, 11, 1781–1785, doi:10.3762/bjoc.11.193
Synthesis and structures of ruthenium–NHC complexes and their catalysis in hydrogen transfer reaction
- Chao Chen,
- Chunxin Lu,
- Qing Zheng,
- Shengliang Ni,
- Min Zhang and
- Wanzhi Chen
Beilstein J. Org. Chem. 2015, 11, 1786–1795, doi:10.3762/bjoc.11.194
Cross-metathesis of polynorbornene with polyoctenamer: a kinetic study
- Yulia I. Denisova,
- Maria L. Gringolts,
- Alexander S. Peregudov,
- Liya B. Krentsel,
- Ekaterina A. Litmanovich,
- Arkadiy D. Litmanovich,
- Eugene Sh. Finkelshtein and
- Yaroslav V. Kudryavtsev
Beilstein J. Org. Chem. 2015, 11, 1796–1808, doi:10.3762/bjoc.11.195
![[Graphic 2]](/bjoc/content/inline/1860-5397-11-195-i10.png?max-width=637&scale=1.18182)
in CHCl3 on the (a) light ...
