Results 31 to 40 of about 90,721 (285)

Facile Photochemical/Thermal Assisted Hydration of Alkynes Catalysed under Aqueous Media by a Chalcogen Stabilized, Robust, Economical, and Reusable Fe₃Se₂(CO)₉ Cluster

Organics, 2023
In this report, the catalytic potential of chalcogen-stabilized iron carbonyl clusters [Fe3E2(CO)9 (E = S, Se, Te)] for the photolytic hydration of alkynes has been explored.
Munsaf Ali, Avinash K. Srivastava, Nitinkumar Satyadev Upadhyay, Naveen Satrawala, Raj K. Joshi   +4 more
doaj   +1 more source

The intermolecular hydro-oxycarbonylation of internal alkynes: current state of the art [PDF]

, 2018
The authors acknowledge the Spanish MINECO (projects CTQ2013-40591-P and CTQ2016-75986-P) and the Gobierno del Principado de Asturias (project GRUPIN14-006) for financial support. J. F.
Cadierno Menéndez, Victorio, Francos Arias, Javier, García Garrido, Sergio Emilio, González Liste, Pedro José   +3 more
core   +2 more sources

Synthesis of Calix[4]arene Appended Lactosylated G1 and Galacto­sylated G2 Generation Glycodendrimers using a ‘CuAAC’ Click Approach

SynOpen, 2023
A modular and highly reliable click approach is applied for the expeditious synthesis of lactose- and galactose-coated calixarene-cored G1 and G2 generation glycodendrimers, respectively.
Sunil Kumar, Mangal S. Yadav, Sumit K. Singh, Sanchayita Rajkhowa, Vinod K. Tiwari   +4 more
doaj   +1 more source

Fluorescent labeling of plasmid DNA and mRNA : gains and losses of current labeling strategies [PDF]

, 2016
Live-cell imaging has provided the life sciences with insights into the cell biology and dynamics. Fluorescent labeling of target molecules proves to be indispensable in this regard. In this Review, we focus on the current fluorescent labeling strategies
Rombouts, Koen, Braeckmans, Kevin, Remaut, Katrien   +2 more
core   +1 more source

Sequential Au(I)-catalyzed reaction of water with o-acetylenyl-substituted phenyldiazoacetates

Beilstein Journal of Organic Chemistry, 2011
The gold(I)-catalyzed reaction of water with o-acetylenyl-substituted phenyldiazoacetates provides 1H-isochromene derivatives in good yields. The reaction follows a catalytic sequence of gold carbene formation/water O–H insertion/alcohol-alkyne ...
Lei Zhou, Yizhou Liu, Yan Zhang, Jianbo Wang   +3 more
doaj   +1 more source

Alkyne lipids as substrates for click chemistry-based in vitro enzymatic assays

Journal of Lipid Research, 2013
Click chemistry is evolving as a powerful tool in biological applications because it allows the sensitive and specific detection of compounds with alkyne or azido groups.
Anne Gaebler, Robin Milan, Leon Straub, Dominik Hoelper, Lars Kuerschner, Christoph Thiele   +5 more
doaj   +1 more source

Synthesis of Polar Aromatic Substituted Terminal Alkynes from Propargyl Amine

Molbank, 2021
A series of small molecules containing polar aromatic substituents and alkynes have been synthesized. One–pot preparations of polar aromatic molecules containing an alkynyl imine and alkynyl amide are reported.
Surya R. Banks, Kyung Min Yoo, Mark E. Welker   +2 more
doaj   +1 more source

Gold(I)-catalyzed hydroarylation reaction of aryl (3-iodoprop-2-yn-1-yl) ethers: synthesis of 3-iodo-2H-chromene derivatives

Beilstein Journal of Organic Chemistry, 2013
An efficient entry to the preparation of elusive 4-unsubstituted-3-iodo-2H-chromenes has been accomplished as result of a catalytic cyclization. Thus, upon exposition of [(3-iodoprop-2-yn-1-yl)oxy]arenes to IPrAuNTf2 (3 mol %), in 1,4-dioxane at 100 °C ...
Pablo Morán-Poladura, Eduardo Rubio, José M. González   +2 more
doaj   +1 more source

Structural Determinants of Alkyne Reactivity in Copper-Catalyzed Azide-Alkyne Cycloadditions

Molecules, 2016
This work represents our initial effort in identifying azide/alkyne pairs for optimal reactivity in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions.
Xiaoguang Zhang, Peiye Liu, Lei Zhu
doaj   +1 more source

Alkene/Alkyne Chemistry #1 [PDF]

, 2015
A mechanism and a synthesis problem related to alkene and alkyne chemistryTwo problems related to alkene and alkyne ...
Snyder, John K.
core   +1 more source