Magnus J Johansson
Overview
Explore the profile of Magnus J Johansson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
40
Citations
400
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Sigmund L, Assante M, Johansson M, Norrby P, Jorner K, Kabeshov M
Chem Sci
. 2025 Mar;
PMID: 40070469
The regio- and site-selectivity of organic reactions is one of the most important aspects when it comes to synthesis planning. Due to that, massive research efforts were invested into computational...
2.
Zakis J, Lipina R, Bell S, Williams S, Mathis M, Johansson M, et al.
ACS Catal
. 2025 Feb;
15(4):3525-3534.
PMID: 40013248
In this work, we present a dedicated, high-throughput reaction optimization platform allowing for the rapid evaluation of regiodivergent C-H borylation protocols while minimizing the amount of starting material required. The...
3.
Wu H, Pan Q, Grill J, Johansson M, Qiu Y, Backvall J
J Am Chem Soc
. 2025 Jan;
147(5):4338-4348.
PMID: 39847037
Direct cross-coupling reactions between two similar unactivated partners are challenging but constitute a powerful strategy for the creation of new carbon-carbon bonds in organic synthesis. [4]Dendralenes are a class of...
4.
Silvi E, Wei W, Johansson M, Himo F, Mendoza A
Chemistry
. 2024 Jun;
30(52):e202402152.
PMID: 38940291
The synthesis of strained carbocyclic building blocks is relevant for Medicinal Chemistry, and methylenecyclobutanes are particularly challenging with current synthetic technology. Careful inspection of the reactivity of [1.1.1]propellane and diboron...
5.
Guillemard L, Ackermann L, Johansson M
Nat Commun
. 2024 Apr;
15(1):3349.
PMID: 38637496
Catalysed C-H activation has emerged as a transformative platform for molecular synthesis and provides new opportunities in drug discovery by late-stage functionalisation (LSF) of complex molecules. Notably, small aliphatic motifs...
6.
Priessner M, Lewis R, Johansson M, Goodman J, Janet J, Tomberg A
J Chem Inf Model
. 2024 Mar;
64(8):3180-3191.
PMID: 38533705
In the pursuit of improved compound identification and database search tasks, this study explores heteronuclear single quantum coherence (HSQC) spectra simulation and matching methodologies. HSQC spectra serve as unique molecular...
7.
Petchey M, Ye Y, Spelling V, Finnigan J, Gittings S, Johansson M, et al.
J Am Chem Soc
. 2024 Feb;
146(7):5005-5010.
PMID: 38329236
Radical hydrofunctionalizations of electronically unbiased dienes are challenging to render regioselective, because the products are nearly identical in energy. Here, we report two engineered FMN-dependent "ene"-reductases (EREDs) that catalyze regiodivergent...
8.
Antermite D, Friis S, Johansson J, Putra O, Ackermann L, Johansson M
Nat Commun
. 2023 Dec;
14(1):8222.
PMID: 38086825
PROteolysis TArgeting Chimeras (PROTACs) are heterobifunctional molecules emerging as a powerful modality in drug discovery, with the potential to address outstanding medical challenges. However, the synthetic feasibility of PROTACs, and...
9.
Sanz-Marco A, Saavedra B, Erbing E, Malmberg J, Johansson M, Martin-Matute B
Org Lett
. 2023 Nov;
26(14):2800-2805.
PMID: 37931032
The acid mediated -iodination of Weinreb amides using a readily available catalyst is described. The selective -iodination of Weinreb amides, challenging substrates in directed C-H activations, and also of benzamides...
10.
Wu H, Zheng Z, Zhang K, Kajanus J, Johansson M, Cordova A, et al.
Angew Chem Int Ed Engl
. 2023 Oct;
62(50):e202314512.
PMID: 37899308
Classical Crabbé type S 2' substitutions of propargylic substrates has served as one of the standard methods for the synthesis of allenes. However, the stereospecific version of this transformation often...