Org. Biomol. Chem., 2023, 21,7799-7807
DOI: 10.1039/D3OB01079A, Paper

Gottam Sreenivasulu, Balasubramanian Sridhar, Galla V. Karunakar
Gold-catalyzed regioselective synthesis of benzofulvenes has been developed from substituted allyloxy 1,5-diynes via 5-endo dig cyclization.
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Org. Biomol. Chem., 2023, 21,7696-7701
DOI: 10.1039/D3OB01256E, Communication

Han Wang, Le Huang, Jun Li, Wenyan Hao
An efficient method for the synthesis of benzo[d]thiazol-2-ylphosphonates via the copper(II)-catalyzed tandem bicyclization of o-halophenyl isothiocyanates and organophosphorus esters.
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Org. Biomol. Chem., 2023, 21,7767-7775
DOI: 10.1039/D3OB01343J, Paper

Open Access

  This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.

Tiago Vinicius Alves, Israel Fernández
The origins of the reactivity and endo/exo selectivity of the Diels–Alder cycloaddition reactions involving furan and substituted furans as dienes have been computationally explored.
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Org. Biomol. Chem., 2023, 21,7776-7781
DOI: 10.1039/D3OB01249B, Paper

Shi-Wei Yu, Zu-Jia Chen, Zhao-Hua Chen, Si-Hong Chen, Kai Yang, Wen-Jin Xu, Zhao-Yang Wang
An efficient and operationally simple synthesis of β-sulfinyl alkenylsulfones through a BF₃·OEt₂-promoted reaction of alkynes and sodium sulfinates is developed.
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Org. Biomol. Chem., 2023, 21,7712-7716
DOI: 10.1039/D3OB01409F, Communication

Chen Liang, Zhibin Chen, Xinyue Hu, Shengxia Yu, Zhenlian Wang, Jiang Cheng
We developed a phosphine-catalyzed ring-opening reaction of cyclopropenones with dicarbonyl compounds as C-nucleophiles, leading to 1,3,3′-tricarbonyl compounds.
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Org. Biomol. Chem., 2023, 21,7791-7798
DOI: 10.1039/D3OB01187A, Paper

Open Access

  This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.

Raquel Hernández-Ruiz, Sara Gómez-Gil, María R. Pedrosa, Samuel Suárez-Pantiga, Roberto Sanz
The one-pot synthesis of haloaromatics from nitroarenes has been accomplished by merging a dioxomolybdenum-catalyzed reduction using pinacol with the Sandmeyer reaction.
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Org. Biomol. Chem., 2023, 21,7821-7830
DOI: 10.1039/D3OB01330H, Paper

Rapeti Thrinadh Kumar, Parameshwar Makam, Naresh Kumar Katari, Ravi K. Kottalanka
A new ecofriendly approach with high yields and it eliminates the need for any hazardous reagents.
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Org. Biomol. Chem., 2023, 21,7666-7680
DOI: 10.1039/D3OB01036H, Review Article

Tomohiro Yasukawa, Katja S. Håheim, Janine Cossy
The synthesis of 1,3-disubstituted bicyclo[1.1.1]pentanes (BCPs), by forming a C–C bond, can be achieved by cross-coupling reaction using transition metal catalysts.
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Org. Biomol. Chem., 2023, 21,7681-7690
DOI: 10.1039/D3OB01382K, Review Article

Michael Andresini, Marco Colella, Leonardo Degennaro, Renzo Luisi
Significant advancements have recently been made in the chemistry of sulfinamidines and sulfinimidate esters. This review aims to provide an overview of the synthetic methods for the preparation and transformation of these overlooked compounds.
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Org. Biomol. Chem., 2023, 21,7852-7872
DOI: 10.1039/D3OB00976A, Review Article

Yuan-Ye Jiang, Chao Chen
This review summarizes the advances in computational studies on Cu-catalyzed aerobic reactions and focuses on the cooperation mechanisms of copper complexes and dioxygen.
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