Beilstein Journal of Organic Chemistry
Overview
The Beilstein Journal of Organic Chemistry is a peer-reviewed open-access journal that publishes high-quality research articles in all areas of organic chemistry. It provides a platform for scientists to share their latest findings, methodologies, and insights in the field. With its rigorous review process and broad scope, the journal serves as a valuable resource for researchers, academics, and professionals in organic chemistry.
Details
Details
Metrics
Metrics
h-index / Ranks: 4277
81
SJR / Ranks: 8665
517
CiteScore / Ranks: 5670
4.60
JIF / Ranks: 3958
2.7
Recent Articles
1.
San L, Balser S, Reeves B, Clikeman T, Chen Y, Strauss S, et al.
Beilstein J Org Chem
. 2025 Mar;
21:515-525.
PMID: 40079025
A new deep-blue emitting and highly fluorescent anthracene (ANTH) derivative containing perfluorobenzyl (Bn) groups, 9,10-ANTH(Bn), was synthesized in a single step reaction of ANTH or ANTH(Br) with BnI, using either...
2.
Gallo G, Lewandowski B
Beilstein J Org Chem
. 2025 Mar;
21:541-546.
PMID: 40079024
Tryptophan fulfills a plethora of important functions in nature both in its free form and as a component of peptides and proteins. Selective binding of tryptophan is therefore important for...
3.
Schachtsiek T, Voss J, Hamsen M, Neumann B, Stammler H, Sewald N
Beilstein J Org Chem
. 2025 Mar;
21:526-532.
PMID: 40079023
Drug conjugates using toxic payloads are a promising approach for selectively combating cancer while sparing healthy tissue. The lack of highly cytotoxic and at the same time selective therapeutics against...
4.
Flemmich L, Micura R
Beilstein J Org Chem
. 2025 Mar;
21:483-489.
PMID: 40079022
The preQ cIass-I riboswitch aptamer can utilize 7-aminomethyl-7-deazaguanine (preQ) ligands that are equipped with an electrophilic handle for the covalent attachment of the ligand to the RNA. The simplicity of...
5.
Dvoracek M, Twamley B, Senge M, Filatov M
Beilstein J Org Chem
. 2025 Mar;
21:500-509.
PMID: 40079021
Bimanes, a class of molecules based on the 1,7-pyrazolo[1,2-]pyrazole-1,7-dione scaffold, were first introduced by E. M. Kosower in 1978. In this study, we report the topochemical cycloaddition of diethyl 2,6-dichloro-1,7-dioxo-1,7-pyrazolo[1,2-a]pyrazole-3,5-dicarboxylate...
6.
Brandt T, Lentes P, Rudtke J, Hosgen M, Nather C, Herges R
Beilstein J Org Chem
. 2025 Mar;
21:490-499.
PMID: 40079020
Diazocines are photoswitches derived from azobenzenes by bridging the two phenyl rings in position with a CHCH group forming an eight membered (diazocine) ring. Diazocine is superior to most azobenzenes...
7.
An B, Wang X, Jiao A, Bian Q, Zhong J
Beilstein J Org Chem
. 2025 Mar;
21:510-514.
PMID: 40079019
Herbst is a destructive stored product pest. The aggregation pheromone of this pest was prepared via a new and effective strategy. The key steps include the ring-opening reaction of chiral...
8.
Guevara-Pulido J, Gonzalez-Perez F, Andres J, Pedrosa R
Beilstein J Org Chem
. 2025 Mar;
21:473-482.
PMID: 40079018
The pharmaceutical chemical industry has long used kinetic resolution to obtain high-value compounds. Organocatalysis has recently been added to this strategy, allowing for the resolution of racemic mixtures with low...
9.
Hostalet-Romero J, Carceller-Ferrer L, Blay G, Sanz-Marco A, Pedro J, Vila C
Beilstein J Org Chem
. 2025 Mar;
21:533-540.
PMID: 40079017
A valuable vinylogous addition reaction between 4-alkylidene-5-aminopyrazoles and alkyl trifluoropyruvates leading to highly functionalized tertiary alcohols bearing a trifluoromethyl group and a pyrazole ring is presented. The corresponding trifluoromethyl alcohols...
10.
Horak Y, Lytvyn R, Vakhula A, Homza Y, Pokhodylo N, Obushak M
Beilstein J Org Chem
. 2025 Mar;
21:444-450.
PMID: 40041199
A new tandem sequence involving the Ugi reaction and Diels-Alder [4 + 2] cycloaddition based on vinylfuran and 1,3-butadienylfuran derivatives was designed and studied. It was found that in the...