Synthesis and reactivity of propargylamines in organic chemistry

K Lauder, A Toscani, N Scalacci… - Chemical reviews, 2017 - ACS Publications
Propargylamines are a versatile class of compounds which find broad application in many
fields of chemistry. This review aims to describe the different strategies developed so far for …

Thiazole derivatives in medicinal chemistry: Recent advancements in synthetic strategies, structure activity relationship and pharmacological outcomes

A Singh, D Malhotra, K Singh, R Chadha… - Journal of Molecular …, 2022 - Elsevier
Thiazole derivatives remains honored heterocycles in the field of medicinal chemistry. This
scaffold has been proven as a universal motif that is present in numerous pharmacologically …

Methods for the direct synthesis of thioesters from aldehydes: a focus review

NH Jabarullah, K Jermsittiparsert… - Journal of Sulfur …, 2020 - Taylor & Francis
Direct C–H bond functionalization chemistry allows the pot-, atom-, and step-economical
and original construction of carbon–carbon and carbon-heteroatom bonds starting from …

Direct Conversion of N-Alkylamines to N-Propargylamines through C–H Activation Promoted by Lewis Acid/Organocopper Catalysis: Application to Late-Stage …

JZ Chan, A Yesilcimen, M Cao, Y Zhang… - Journal of the …, 2020 - ACS Publications
An efficient catalytic method to convert an α-C–H bond of N-alkylamines into an α-C–alkynyl
bond was developed. In the past, such transformations were carried out under oxidative …

Three-component coupling of CO2, propargyl alcohols, and amines: An environmentally benign access to cyclic and acyclic carbamates (A Review)

S Arshadi, E Vessally, A Hosseinian… - Journal of CO2 …, 2017 - Elsevier
Carbamates are key intermediates in the synthesis of a variety of pharmaceutically important
compounds and fine chemicals. Moreover, they have been widely applied as chiral …

Direct CH trifluoromethylthiolation of (hetero) arenes: a review

M Hamzehloo, A Hosseinian, S Ebrahimiasl… - Journal of Fluorine …, 2019 - Elsevier
This review highlights up-to-date developments and achievements in direct
trifluoromethylthiolation of (hetero) aryl Csingle bond H bonds with particular emphasis on …

[HTML][HTML] Intermolecular difunctionalization of alkenes: synthesis of β-hydroxy sulfides

B Azizi, MRP Heravi, Z Hossaini, A Ebadi, E Vessally - RSC advances, 2021 - pubs.rsc.org
Direct difunctionalization of carbon–carbon double bonds is one of the most powerful tools
available for concomitant introduction of two functional groups into olefinic substrates. In this …

Cross-Dehydrogenative C–H/S–H Coupling Reactions

A Hosseinian, S Ahmadi, FAH Nasab… - Topics in Current …, 2018 - Springer
Carbon–sulfur bond formation represents a key step in the synthesis of thioethers, which are
a common structural motif in many pharmaceutically compounds. The direct cross …

[HTML][HTML] Recent developments in decarboxylative cross-coupling reactions between carboxylic acids and N–H compounds

S Arshadi, S Ebrahimiasl, A Hosseinian, A Monfared… - RSC …, 2019 - pubs.rsc.org
Carboxylic acids and their derivatives are ubiquitous compounds in organic chemistry, and
are widely commercially available in a large structural variety. Recently, carboxylic acids …

[HTML][HTML] Direct synthesis of sulfenamides, sulfinamides, and sulfonamides from thiols and amines

Y Cao, S Abdolmohammadi, R Ahmadi, A Issakhov… - RSC …, 2021 - pubs.rsc.org
Needless to say that organosulfur compounds with sulfur–nitrogen bonds have found
various applications in diverse fields such as pharmaceuticals, agrochemicals, polymers …