Volume No. 18

2022

Pages 1 - 1771

Table of Contents

124 Full Research Paper
17 Review
31 Letter
5 Perspective
1 Commentary
7 Editorial
  • Editorial
  • Published 26 Oct 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1505–1506, doi:10.3762/bjoc.18.158

  • Full Research Paper
  • Published 27 Oct 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1507–1517, doi:10.3762/bjoc.18.159

  • Letter
  • Published 07 Nov 2022
Graphical Abstract

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

  1. Elenilson F. da Silva,
  2. Krist Helen Antunes Fernandes,
  3. Denise Diedrich,
  4. Jessica Gotardi,
  5. Marcia Silvana Freire Franco,
  6. Carlos Henrique Tomich de Paula da Silva,
  7. Ana Paula Duarte de Souza and
  8. Simone Cristina Baggio Gnoatto
  • Full Research Paper
  • Published 09 Nov 2022

  • PDF

  • Supp. Info
Graphical Abstract

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

  1. Pavel A. Topanov,
  2. Anna A. Maslivets,
  3. Maksim V. Dmitriev,
  4. Irina V. Mashevskaya,
  5. Yurii V. Shklyaev and
  6. Andrey N. Maslivets
  • Full Research Paper
  • Published 10 Nov 2022

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  • Supp. Info
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1532–1538, doi:10.3762/bjoc.18.162

  • Full Research Paper
  • Published 11 Nov 2022
Graphical Abstract

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

  1. Sasha Hayes,
  2. Aya C. Taki,
  3. Kah Yean Lum,
  4. Joseph J. Byrne,
  5. Merrick G. Ekins,
  6. Robin B. Gasser and
  7. Rohan A. Davis
  • Full Research Paper
  • Published 15 Nov 2022

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  • Supp. Info
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1544–1552, doi:10.3762/bjoc.18.164

  • Full Research Paper
  • Published 17 Nov 2022
Graphical Abstract

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

  1. Takumi Matsumoto,
  2. Takefumi Kuranaga,
  3. Yuto Taniguchi,
  4. Weicheng Wang and
  5. Hideaki Kakeya
  • Full Research Paper
  • Published 18 Nov 2022
Graphical Abstract

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)

  1. Yukiko Karuo,
  2. Atsushi Tarui,
  3. Kazuyuki Sato,
  4. Kentaro Kawai and
  5. Masaaki Omote
  • Full Research Paper
  • Published 21 Nov 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1567–1574, doi:10.3762/bjoc.18.167

  • Review
  • Published 22 Nov 2022

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Graphical Abstract

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

  1. Jiayue Fu,
  2. Bingbing Li,
  3. Zefang Zhou,
  4. Maosheng Cheng,
  5. Lu Yang and
  6. Yongxiang Liu
  • Letter
  • Published 23 Nov 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1589–1595, doi:10.3762/bjoc.18.169

  • Full Research Paper
  • Published 25 Nov 2022

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  • Supp. Info
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1596–1606, doi:10.3762/bjoc.18.170

One-pot double annulations to confer diastereoselective spirooxindolepyrrolothiazoles

  1. Juan Lu,
  2. Bin Yao,
  3. Desheng Zhan,
  4. Zhuo Sun,
  5. Yun Ji and
  6. Xiaofeng Zhang
  • Full Research Paper
  • Published 28 Nov 2022

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  • Supp. Info
Graphical Abstract

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

  1. Raphael Bereiter,
  2. Marco Oberlechner and
  3. Ronald Micura
  • Full Research Paper
  • Published 29 Nov 2022

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  • Supp. Info
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1617–1624, doi:10.3762/bjoc.18.172

Synthetic study toward the diterpenoid aberrarone

  1. Liang Shi,
  2. Zhiyu Gao,
  3. Yiqing Li,
  4. Yuanhao Dai,
  5. Yu Liu,
  6. Lili Shi and
  7. Hong-Dong Hao
  • Letter
  • Published 30 Nov 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1625–1628, doi:10.3762/bjoc.18.173

  • Full Research Paper
  • Published 01 Dec 2022

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  • Supp. Info
Graphical Abstract

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

  1. Ksenia Malkova,
  2. Andrey Bubyrev,
  3. Vasilisa Krivovicheva,
  4. Dmitry Dar’in,
  5. Alexander Bunev and
  6. Mikhail Krasavin
  • Letter
  • Published 02 Dec 2022

  • PDF

  • Supp. Info
Graphical Abstract

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

  1. Motoyuki Isoda,
  2. Kazuyuki Sato,
  3. Kenta Kameda,
  4. Kana Wakabayashi,
  5. Ryota Sato,
  6. Hideki Minami,
  7. Yukiko Karuo,
  8. Atsushi Tarui,
  9. Kentaro Kawai and
  10. Masaaki Omote
  • Full Research Paper
  • Published 02 Dec 2022

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  • Supp. Info
Graphical Abstract

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

  1. Anastasia Vepreva,
  2. Alexander Yanovich,
  3. Dmitry Dar’in,
  4. Grigory Kantin,
  5. Alexander Bunev and
  6. Mikhail Krasavin
  • Full Research Paper
  • Published 06 Dec 2022

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  • Supp. Info
Graphical Abstract

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

  1. Friederike Biermann,
  2. Sebastian L. Wenski and
  3. Eric J. N. Helfrich
  • Perspective
  • Published 06 Dec 2022

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Graphical Abstract

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

  1. Elena R. Lopat’eva,
  2. Igor B. Krylov,
  3. Dmitry A. Lapshin and
  4. Alexander O. Terent’ev
  • Perspective
  • Published 09 Dec 2022

  • PDF
Graphical Abstract

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.

  1. Ye-Qing Du,
  2. Heng Li,
  3. Quan Xu,
  4. Wei Tang,
  5. Zai-Yong Zhang,
  6. Ming-Zhi Su,
  7. Xue-Ting Liu and
  8. Yue-Wei Guo
  • Full Research Paper
  • Published 09 Dec 2022

  • PDF

  • Supp. Info
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1696–1706, doi:10.3762/bjoc.18.180

Total synthesis of grayanane natural products

  1. Nicolas Fay,
  2. Rémi Blieck,
  3. Cyrille Kouklovsky and
  4. Aurélien de la Torre
  • Review
  • Published 12 Dec 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1707–1719, doi:10.3762/bjoc.18.181

  • Perspective
  • Published 16 Dec 2022

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Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1720–1740, doi:10.3762/bjoc.18.182

Synthetic study toward tridachiapyrone B

  1. Morgan Cormier,
  2. Florian Hernvann and
  3. Michaël De Paolis
  • Full Research Paper
  • Published 19 Dec 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1741–1748, doi:10.3762/bjoc.18.183

  • Full Research Paper
  • Published 22 Dec 2022

  • PDF

  • Supp. Info
Graphical Abstract

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

  1. Adwoa P. Nartey,
  2. Aboagye K. Dofuor,
  3. Kofi B. A. Owusu,
  4. Anil S. Camas,
  5. Hai Deng,
  6. Marcel Jaspars and
  7. Kwaku Kyeremeh
  • Full Research Paper
  • Published 28 Dec 2022
Graphical Abstract

Beilstein J. Org. Chem. 2022, 18, 1763–1771, doi:10.3762/bjoc.18.185

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