Org. Biomol. Chem., 2023, 21,7924-7927
DOI: 10.1039/D3OB01415K, Paper

Open Access

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

Olga Bakhanovich, Blanka Klepetářová, Petr Beier
N-(Per)fluoroalkyl indoles are accessed by rhodium(II)-catalyzed transannulation of 4-cyclohexenyl 1,2,3-triazoles, followed by oxidation of the intermediate indolines.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,8003-8019
DOI: 10.1039/D3OB01231J, Paper

Ann-Kathrin Bauer, Jürgen Conrad, Uwe Beifuss
The CuI-catalyzed reaction between one 1,2-bis(2-bromoaryl)hydrazine moiety and two 1,3-diketones delivers substituted 1,1′-bisindoles with yields up to 92%.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,7944-7953
DOI: 10.1039/D3OB01472J, Paper

Somporn Palasarn, Thapanee Pruksatrakul, Wilunda Choowong, Natthawut Wiriyathanawudhiwong, Thitiya Boonpratuang, Panida Surawatanawong, Chawanee Thongpanchang, Masahiko Isaka
Oudemansin and 9-methoxystrobilurin derivatives with potent antimalarial activity were isolated from cultures of the basidiomycete Favolaschia minutissima. A method for semisynthetic modification was demonstrated.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,7928-7934
DOI: 10.1039/D3OB01237A, Paper

Lenida Kyndiah, Fillip Kumar Sarkar, Sushmita Gajurel, Rajib Sarkar, Jasha Momo H. Anal, Amarta Kumar Pal
Pd@GO catalysed stereo- and regio-selective addition of arenes to alkynes via C–H bond functionalization and coumarin synthesis.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, Advance Article
DOI: 10.1039/D3OB01115A, Review Article

Hong Guo, Bei Zhou, Jingjing Chang, Wenxu Chang, Jiyao Feng, Zhenhua Zhang
The review focus on multicomponent reactions of azides for the construction of N-heterocycles in recent 10 years.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,7913-7916
DOI: 10.1039/D3OB01281F, Communication

Jianlin Zou, Hongye Li, Zilong Wang, Min Ye
Two efficient and selective glycosyltransferases were identified from Sophora japonica L.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, Advance Article
DOI: 10.1039/D3OB01451G, Paper

Zhengyu Han, Yu Xue, Xiang Li, Xinzhe Hu, Xiu-Qin Dong, Jianwei Sun, Hai Huang
A new kind of indole-fused zwitterionic π-allylpalladium precursor compound has been designed and synthesized.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,8020-8030
DOI: 10.1039/D3OB01319G, Paper

Dipanjan Banik, Anirban Karak, Satyajit Halder, Shilpita Banerjee, Moumi Mandal, Anwesha Maiti, Kuladip Jana, Ajit Kumar Mahapatra
A turn-on fluorescent probe TPB-NO₂ was synthesized for rapid detection of H₂S in environmental and biological samples. A bright cyan colour was observed due to the PET mechanism.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, 21,7984-7993
DOI: 10.1039/D3OB00237C, Paper

Diana Sloboda, Cameron C. Weber, Eduards Bakis
In this study, we discovered that both the structure of the ionic liquid and the catalyst exert a significant influence on the copper(I)-catalyzed azide–alkyne cycloaddition reaction rate.
The content of this RSS Feed (c) The Royal Society of Chemistry

Org. Biomol. Chem., 2023, Advance Article
DOI: 10.1039/D3OB01289A, Paper

Yucai Tang, Jinglin Duan, Biyu Yang, Yupeng He, Changyuan Du, Xiangyang Zhang
An efficient visible-light-promoted organic-dye-catalyzed radical cascade cyclization was developed for the rapid synthesis of sulfonyl-substituted indolo[2,1-a]isoquinolines and benzimidazo[2,1-a]isoquinolin-6(5H)-ones.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry