Synthesis
Overview
Synthesis is a multidisciplinary journal that publishes cutting-edge research in the fields of chemistry, biology, and materials science. It provides a platform for scientists to share their innovative synthetic methodologies, strategies, and techniques, fostering collaboration and advancing knowledge in the synthesis of organic and inorganic compounds, natural products, pharmaceuticals, and functional materials. With a focus on originality and quality, Synthesis serves as a valuable resource for researchers, academics, and industry professionals seeking to stay at the forefront of synthetic s
Details
Details
Metrics
Metrics
h-index / Ranks: 1321
155
SJR / Ranks: 7756
582
CiteScore / Ranks: 4922
5.10
JIF / Ranks: 4138
2.6
Recent Articles
1.
Chen J, Chao D, Tran U, Billingsley K
Synthesis (Stuttg)
. 2025 Feb;
56(18):2909-2917.
PMID: 39896865
Hyperpolarized C magnetic resonance spectroscopy can provide unique insights into metabolic activity . Despite the advantages of this technology, certain metabolic pathways such as the tricarboxylic acid (TCA) cycle are...
2.
Kim Y, Jacobson K
Synthesis (Stuttg)
. 2025 Jan;
2000(1):119-122.
PMID: 39816948
A versatile and convenient procedure for the functional derivatization with carbon substituents at the 6-position of pyridoxal using a Grignard reaction upon a protected -isobutoxycarbony-loxypyridoxal chloride and Heck reactions with...
3.
Croll E, Kwon O
Synthesis (Stuttg)
. 2024 Dec;
56(12):1843-1850.
PMID: 39711915
The Mitsunobu reaction is one the most widely known reactions in the organic chemistry canon. Despite its fame, some aspects of the mechanism remain poorly understood, 55 years after its...
4.
Martin B, Ma D, Saito T, Gallagher K, Dai M
Synthesis (Stuttg)
. 2024 Dec;
56(1):107-117.
PMID: 39669741
alkaloid complanadine A, isolated by Kobayashi et al. in 2000, is a complex and unsymmetrical dimer of lycodine. Biologically, it is a novel and promising lead compound for the development...
5.
Chacon-Teran M, Bhattacharjee S, Bailoo J, Deonarine A, Findlater M
Synthesis (Stuttg)
. 2024 Sep;
55(24):4091-4095.
PMID: 39345355
Robust and reliable synthetic methods have been developed for the preparation of an arseno-fatty acid (As-FA362) and an arseno-hydrocarbon (As-HC444). An improved route to access the starting materials necessary for...
6.
Eschliman K, Bossmann S
Synthesis (Stuttg)
. 2024 Aug;
51(8):1746-1752.
PMID: 39193180
Isothiocyanates (ICTs) are a group of molecules that can be used for many different purposes, they exhibit anticancer, antimicrobial, antibiotic, and anti-inflammatory properties. The synthesis of isothiocyanates has been a...
7.
Hussain W, Parasram M
Synthesis (Stuttg)
. 2024 Aug;
56(11):1775-1786.
PMID: 39144683
Oxidative cleavage of alkenes leading to valuable carbonyl derivatives is a fundamental transformation in synthetic chemistry. In particular, ozonolysis is the mainstream method for the oxidative cleavage of alkenes that...
8.
Aquilina J, Smith M
Synthesis (Stuttg)
. 2024 Jul;
55(22):3725-3736.
PMID: 39081875
The alkaloids are a relatively small family of plant-derived alkaloids that present an intriguing array of structural intricacy and biological properties. As such, these natural products have drawn interest from...
9.
Zhu H, Driver T
Synthesis (Stuttg)
. 2024 Jul;
54(14):3142-3161.
PMID: 39076505
Recent advances in the development of reductive reactions of nitroarenes using organomagnesium-, organozinc-, and single electron transfer reagents is discussed within this review. The review is divided into the following...
10.
Treacy S, Rovis T
Synthesis (Stuttg)
. 2024 Jul;
56(13):1967-1978.
PMID: 38962497
The absorption of light by photosensitizers has been shown to offer novel reactive pathways through electronic excited state intermediates, complementing ground state mechanisms. Such strategies have been applied in both...