Molecular and macromolecular electrochemistry: synthesis, mechanism, and redox properties
- Shinsuke Inagi and
- Mahito Atobe
Beilstein J. Org. Chem. 2022, 18, 1505–1506, doi:10.3762/bjoc.18.158
Cyclometalated iridium complexes-catalyzed acceptorless dehydrogenative coupling reaction: construction of quinoline derivatives and evaluation of their antimicrobial activities
- Hongling Shui,
- Yuhong Zhong,
- Renshi Luo,
- Zhanyi Zhang,
- Jiuzhong Huang,
- Ping Yang and
- Nianhua Luo
Beilstein J. Org. Chem. 2022, 18, 1507–1517, doi:10.3762/bjoc.18.159
An alternative C–P cross-coupling route for the synthesis of novel V-shaped aryldiphosphonic acids
- Stephen J. I. Shearan,
- Enrico Andreoli and
- Marco Taddei
Beilstein J. Org. Chem. 2022, 18, 1518–1523, doi:10.3762/bjoc.18.160
New triazole-substituted triterpene derivatives exhibiting anti-RSV activity: synthesis, biological evaluation, and molecular modeling
- Elenilson F. da Silva,
- Krist Helen Antunes Fernandes,
- Denise Diedrich,
- Jessica Gotardi,
- Marcia Silvana Freire Franco,
- Carlos Henrique Tomich de Paula da Silva,
- Ana Paula Duarte de Souza and
- Simone Cristina Baggio Gnoatto
Beilstein J. Org. Chem. 2022, 18, 1524–1531, doi:10.3762/bjoc.18.161
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
- Pavel A. Topanov,
- Anna A. Maslivets,
- Maksim V. Dmitriev,
- Irina V. Mashevskaya,
- Yurii V. Shklyaev and
- Andrey N. Maslivets
Beilstein J. Org. Chem. 2022, 18, 1532–1538, doi:10.3762/bjoc.18.162
Efficient synthesis of aziridinecyclooctanediol and 3-aminocyclooctanetriol
- Emine Salamci and
- Ayse Kilic Lafzi
Beilstein J. Org. Chem. 2022, 18, 1539–1543, doi:10.3762/bjoc.18.163
Using UHPLC–MS profiling for the discovery of new sponge-derived metabolites and anthelmintic screening of the NatureBank bromotyrosine library
- Sasha Hayes,
- Aya C. Taki,
- Kah Yean Lum,
- Joseph J. Byrne,
- Merrick G. Ekins,
- Robin B. Gasser and
- Rohan A. Davis
Beilstein J. Org. Chem. 2022, 18, 1544–1552, doi:10.3762/bjoc.18.164
A study of the DIBAL-promoted selective debenzylation of α-cyclodextrin protected with two different benzyl groups
- Naser-Abdul Yousefi,
- Morten L. Zimmermann and
- Mikael Bols
Beilstein J. Org. Chem. 2022, 18, 1553–1559, doi:10.3762/bjoc.18.165
Solid-phase total synthesis and structural confirmation of antimicrobial longicatenamide A
- Takumi Matsumoto,
- Takefumi Kuranaga,
- Yuto Taniguchi,
- Weicheng Wang and
- Hideaki Kakeya
Beilstein J. Org. Chem. 2022, 18, 1560–1566, doi:10.3762/bjoc.18.166
Simple synthesis of multi-halogenated alkenes from 2-bromo-2-chloro-1,1,1-trifluoroethane (halothane)
- Yukiko Karuo,
- Atsushi Tarui,
- Kazuyuki Sato,
- Kentaro Kawai and
- Masaaki Omote
Beilstein J. Org. Chem. 2022, 18, 1567–1574, doi:10.3762/bjoc.18.167
Functionalization of imidazole N-oxide: a recent discovery in organic transformations
- Koustav Singha,
- Imran Habib and
- Mossaraf Hossain
Beilstein J. Org. Chem. 2022, 18, 1575–1588, doi:10.3762/bjoc.18.168
Formal total synthesis of macarpine via a Au(I)-catalyzed 6-endo-dig cycloisomerization strategy
- Jiayue Fu,
- Bingbing Li,
- Zefang Zhou,
- Maosheng Cheng,
- Lu Yang and
- Yongxiang Liu
Beilstein J. Org. Chem. 2022, 18, 1589–1595, doi:10.3762/bjoc.18.169
Preparation of β-cyclodextrin-based dimers with selectively methylated rims and their use for solubilization of tetracene
- Konstantin Lebedinskiy,
- Volodymyr Lobaz and
- Jindřich Jindřich
Beilstein J. Org. Chem. 2022, 18, 1596–1606, doi:10.3762/bjoc.18.170
One-pot double annulations to confer diastereoselective spirooxindolepyrrolothiazoles
- Juan Lu,
- Bin Yao,
- Desheng Zhan,
- Zhuo Sun,
- Yun Ji and
- Xiaofeng Zhang
Beilstein J. Org. Chem. 2022, 18, 1607–1616, doi:10.3762/bjoc.18.171
A new route for the synthesis of 1-deazaguanine and 1-deazahypoxanthine
- Raphael Bereiter,
- Marco Oberlechner and
- Ronald Micura
Beilstein J. Org. Chem. 2022, 18, 1617–1624, doi:10.3762/bjoc.18.172
Synthetic study toward the diterpenoid aberrarone
- Liang Shi,
- Zhiyu Gao,
- Yiqing Li,
- Yuanhao Dai,
- Yu Liu,
- Lili Shi and
- Hong-Dong Hao
Beilstein J. Org. Chem. 2022, 18, 1625–1628, doi:10.3762/bjoc.18.173
Synthesis of (−)-halichonic acid and (−)-halichonic acid B
- Keith P. Reber and
- Emma L. Niner
Beilstein J. Org. Chem. 2022, 18, 1629–1635, doi:10.3762/bjoc.18.174
A novel bis-triazole scaffold accessed via two tandem [3 + 2] cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction
- Ksenia Malkova,
- Andrey Bubyrev,
- Vasilisa Krivovicheva,
- Dmitry Dar’in,
- Alexander Bunev and
- Mikhail Krasavin
Beilstein J. Org. Chem. 2022, 18, 1636–1641, doi:10.3762/bjoc.18.175
Rhodium-catalyzed intramolecular reductive aldol-type cyclization: Application for the synthesis of a chiral necic acid lactone
- Motoyuki Isoda,
- Kazuyuki Sato,
- Kenta Kameda,
- Kana Wakabayashi,
- Ryota Sato,
- Hideki Minami,
- Yukiko Karuo,
- Atsushi Tarui,
- Kentaro Kawai and
- Masaaki Omote
Beilstein J. Org. Chem. 2022, 18, 1642–1648, doi:10.3762/bjoc.18.176
A novel spirocyclic scaffold accessed via tandem Claisen rearrangement/intramolecular oxa-Michael addition
- Anastasia Vepreva,
- Alexander Yanovich,
- Dmitry Dar’in,
- Grigory Kantin,
- Alexander Bunev and
- Mikhail Krasavin
Beilstein J. Org. Chem. 2022, 18, 1649–1655, doi:10.3762/bjoc.18.177
Navigating and expanding the roadmap of natural product genome mining tools
- Friederike Biermann,
- Sebastian L. Wenski and
- Eric J. N. Helfrich
Beilstein J. Org. Chem. 2022, 18, 1656–1671, doi:10.3762/bjoc.18.178
Redox-active molecules as organocatalysts for selective oxidative transformations – an unperceived organocatalysis field
- Elena R. Lopat’eva,
- Igor B. Krylov,
- Dmitry A. Lapshin and
- Alexander O. Terent’ev
Beilstein J. Org. Chem. 2022, 18, 1672–1695, doi:10.3762/bjoc.18.179
New cembrane-type diterpenoids with anti-inflammatory activity from the South China Sea soft coral Sinularia sp.
- Ye-Qing Du,
- Heng Li,
- Quan Xu,
- Wei Tang,
- Zai-Yong Zhang,
- Ming-Zhi Su,
- Xue-Ting Liu and
- Yue-Wei Guo
Beilstein J. Org. Chem. 2022, 18, 1696–1706, doi:10.3762/bjoc.18.180
Total synthesis of grayanane natural products
- Nicolas Fay,
- Rémi Blieck,
- Cyrille Kouklovsky and
- Aurélien de la Torre
Beilstein J. Org. Chem. 2022, 18, 1707–1719, doi:10.3762/bjoc.18.181
Inline purification in continuous flow synthesis – opportunities and challenges
- Jorge García-Lacuna and
- Marcus Baumann
Beilstein J. Org. Chem. 2022, 18, 1720–1740, doi:10.3762/bjoc.18.182
Synthetic study toward tridachiapyrone B
- Morgan Cormier,
- Florian Hernvann and
- Michaël De Paolis
Beilstein J. Org. Chem. 2022, 18, 1741–1748, doi:10.3762/bjoc.18.183
Inclusion complexes of the steroid hormones 17β-estradiol and progesterone with β- and γ-cyclodextrin hosts: syntheses, X-ray structures, thermal analyses and API solubility enhancements
- Alexios I. Vicatos,
- Zakiena Hoossen and
- Mino R. Caira
Beilstein J. Org. Chem. 2022, 18, 1749–1762, doi:10.3762/bjoc.18.184
Digyalipopeptide A, an antiparasitic cyclic peptide from the Ghanaian Bacillus sp. strain DE2B
- Adwoa P. Nartey,
- Aboagye K. Dofuor,
- Kofi B. A. Owusu,
- Anil S. Camas,
- Hai Deng,
- Marcel Jaspars and
- Kwaku Kyeremeh
Beilstein J. Org. Chem. 2022, 18, 1763–1771, doi:10.3762/bjoc.18.185
