Benign by design: catalyst-free in-water, on-water green chemical methodologies in organic synthesis

MB Gawande, VDB Bonifácio, R Luque… - Chemical Society …, 2013 - pubs.rsc.org
Catalyst-free reactions developed during the last decade and the latest developments in this
emerging field are summarized with a focus on catalyst-free reactions in-water and on-water …

Microwave assisted organic synthesis—a review

P Lidström, J Tierney, B Wathey, J Westman - Tetrahedron, 2001 - Elsevier
In the electromagnetic spectrum, the microwave radiation region is located between infrared
radiation and radio waves. Microwaves have wavelengths of 1 mm±1 m, corresponding to …

Use of Lawesson's reagent in organic syntheses

T Ozturk, E Ertas, O Mert - Chemical reviews, 2007 - ACS Publications
Transformation of a carbonyl functional group into thiocarbonyl has been an important
interest to synthetic organic chemists for many years. Two reagents, phosphorus …

Microwave-assisted high-speed chemistry: a new technique in drug discovery

M Larhed, A Hallberg - Drug discovery today, 2001 - Elsevier
In both lead identification and lead optimization processes there is an acute need for new
organic small molecules. Traditional methods of organic synthesis are orders of magnitude …

Solvent-free accelerated organic syntheses using microwaves

RS Varma - Pure and Applied Chemistry, 2001 - degruyter.com
A solvent-free approach for organic synthesis is described which involves microwave (MW)
exposure of neat reactants (undiluted) either in the presence of a catalyst or catalyzed by the …

Recent advances in photocatalytic C–S/P–S bond formation via the generation of sulfur centered radicals and functionalization

W Guo, K Tao, W Tan, M Zhao, L Zheng… - Organic Chemistry …, 2019 - pubs.rsc.org
Thioyl and sulfonyl radicals are usually produced from various thiols and sulfonyl derivatives
in high efficiency by single-electron-transfer (SET) oxidation. The generated sulfur …

(−)-Cytisine and derivatives: synthesis, reactivity, and applications

J Rouden, MC Lasne, J Blanchet, J Baudoux - Chemical reviews, 2014 - ACS Publications
(−)-Cytisine (−)-1,[(1R, 5S)-1, 2, 3, 4, 5, 6-hexahydro-1, 5-methano-8H-pyrido [1, 2a][1, 5]
diazocin-8-one (Figure 1), is an alkaloid extracted from various plants belonging to the …

Thionation using fluorous Lawesson's reagent

Z Kaleta, BT Makowski, T Soós, R Dembinski - Organic Letters, 2006 - ACS Publications
Thionation of amides, 1, 4-diketones, N-(2-oxoalkyl) amides, N, N '-acylhydrazines, and acyl-
protected uridines with the use of a fluorous analogue of the Lawesson's reagent leads to …

Benzothiazoles with tunable electron-withdrawing strength and reverse polarity: a route to triphenylamine-based chromophores with enhanced two-photon absorption

P Hrobárik, V Hrobáriková, I Sigmundová… - The Journal of …, 2011 - ACS Publications
A series of dipolar and octupolar triphenylamine-derived dyes containing a benzothiazole
positioned in the matched or mismatched fashion have been designed and synthesized via …

Selenium-containing chrysin and quercetin derivatives: Attractive scaffolds for cancer therapy

IL Martins, C Charneira, V Gandin… - Journal of Medicinal …, 2015 - ACS Publications
Selenium-containing chrysin (SeChry) and 3, 7, 3′, 4′-tetramethylquercetin (SePQue)
derivatives were synthesized by a microwave-based methodology. In addition to their …