One-Pot Synthesis of Triazoles from Organic Halides and Alkynes in Nonionic Nanomicelles at Room Temperature
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
One-Pot Synthesis of Triazoles from Organic Halides and Alkynes in Nonionic Nanomicelles at Room Temperature
Authors
Keywords
-
Journal
Asian Journal of Organic Chemistry
Volume 3, Issue 12, Pages 1278-1283
Publisher
Wiley
Online
2014-10-06
DOI
10.1002/ajoc.201402153
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Copper Immobilized on Nanosilica Triazine Dendrimer (Cu(II)-TD@nSiO2)-Catalyzed Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles and Bis- and Tris-Triazoles via a One-Pot Multicomponent Click Reaction
- (2014) Mahboobeh Nasr-Esfahani et al. JOURNAL OF ORGANIC CHEMISTRY
- “Nok”: A Phytosterol-Based Amphiphile Enabling Transition-Metal-Catalyzed Couplings in Water at Room Temperature
- (2014) Piyatida Klumphu et al. JOURNAL OF ORGANIC CHEMISTRY
- Leveraging the Micellar Effect: Gold-Catalyzed Dehydrative Cyclizations in Water at Room Temperature
- (2014) Stefan R. K. Minkler et al. ORGANIC LETTERS
- Click Chemistry Based Functionalizations of Nucleoside, Nucleotide and Nucleic Acids
- (2013) Anilkumar Kore et al. CURRENT ORGANIC CHEMISTRY
- The Synthesis of Tetrazoles in Nanometer Aqueous Micelles at Room Temperature
- (2013) Aming Xie et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Copper on chitosan: a recyclable heterogeneous catalyst for azide–alkyne cycloaddition reactions in water
- (2013) R. B. Nasir Baig et al. GREEN CHEMISTRY
- Synthesis and Biological Applications of Triazole Derivatives – A Review
- (2013) S. Sathish Kumar et al. MINI-REVIEWS IN ORGANIC CHEMISTRY
- Group XII Metal–N-Heterocyclic Carbene Complexes: Synthesis, Structural Diversity, Intramolecular Interactions, and Applications
- (2013) Srinivasa Budagumpi et al. ORGANOMETALLICS
- Rhodium-Catalyzed Asymmetric 1,4-Additions, in Water at Room Temperature, with In-Flask Catalyst Recycling
- (2012) Bruce H. Lipshutz et al. ADVANCED SYNTHESIS & CATALYSIS
- Inhibition of NaV1.6 sodium channel currents by a novel series of 1,4-disubstituted-triazole derivatives obtained via copper-catalyzed click chemistry
- (2012) Mirko Rivara et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Copper-Catalyzed Azide–Alkyne Cycloaddition Reaction in Water Using Cyclodextrin as a Phase Transfer Catalyst
- (2012) Jung-Ah Shin et al. JOURNAL OF ORGANIC CHEMISTRY
- C–C Bond Formation via Copper-Catalyzed Conjugate Addition Reactions to Enones in Water at Room Temperature
- (2012) Bruce H. Lipshutz et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Gold Catalysis in Micellar Systems
- (2011) Stefan R. K. Minkler et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- The First Well-Defined Silver(I)-Complex-Catalyzed Cycloaddition of Azides onto Terminal Alkynes at Room Temperature
- (2011) James McNulty et al. CHEMISTRY-A EUROPEAN JOURNAL
- [CuBr(PPh3)3] for Azide−Alkyne Cycloaddition Reactions under Strict Click Conditions
- (2011) Steven Lal et al. JOURNAL OF ORGANIC CHEMISTRY
- TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
- (2011) Bruce H. Lipshutz et al. JOURNAL OF ORGANIC CHEMISTRY
- A Copper(I) Isonitrile Complex as a Heterogeneous Catalyst for Azide−Alkyne Cycloaddition in Water
- (2011) Meina Liu et al. ORGANIC LETTERS
- Effect of temperature on triazole and bistriazole formation through copper-catalyzed alkyne–azide cycloaddition
- (2011) Jaime González et al. TETRAHEDRON LETTERS
- Direct Synthesis of 1,4-Disubstituted-5-alumino-1,2,3-triazoles: Copper-Catalyzed Cycloaddition of Organic Azides and Mixed Aluminum Acetylides
- (2010) Yuhan Zhou et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Click chemistry inspired one-pot synthesis of 1,4-disubstituted 1,2,3-triazoles and their Src kinase inhibitory activity
- (2010) Dalip Kumar et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Click polymerization
- (2010) Anjun Qin et al. CHEMICAL SOCIETY REVIEWS
- Synthesis and cytotoxicity evaluation of novel 1,4-disubstituted 1,2,3-triazoles via CuI catalysed 1,3-dipolar cycloaddition
- (2010) Jyothi Vantikommu et al. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
- Unsupported Copper Nanoparticles in the 1,3-Dipolar Cycloaddition of Terminal Alkynes and Azides
- (2010) Francisco Alonso et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Carboxylic Acid-Promoted Copper(I)-Catalyzed Azide−Alkyne Cycloaddition
- (2010) Changwei Shao et al. JOURNAL OF ORGANIC CHEMISTRY
- Facile Synthesis of Nitrogen Tetradentate Ligands and Their Applications in CuI-Catalyzed N-Arylation and Azide-Alkyne Cycloaddition
- (2009) Fuwei Li et al. CHEMISTRY-A EUROPEAN JOURNAL
- Highly active copper-catalysts for azide-alkynecycloaddition
- (2009) Zsombor Gonda et al. DALTON TRANSACTIONS
- Huisgen Cycloaddition Reaction ofC-Alkynyl Ribosides under Micellar Catalysis: Synthesis of Ribavirin Analogues
- (2009) Ramzi Aït Youcef et al. JOURNAL OF ORGANIC CHEMISTRY
- Apparent Copper(II)-Accelerated Azide−Alkyne Cycloaddition
- (2009) Wendy S. Brotherton et al. ORGANIC LETTERS
- A Highly Active Catalyst for Huisgen 1,3-Dipolar Cycloadditions Based on the Tris(triazolyl)methanol−Cu(I) Structure
- (2009) Salih Özçubukçu et al. ORGANIC LETTERS
- A facile and regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles using click chemistry
- (2009) Dalip Kumar et al. TETRAHEDRON LETTERS
- Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles†
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Heck Couplings at Room Temperature in Nanometer Aqueous Micelles†
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Micellar Catalysis of Suzuki−Miyaura Cross-Couplings with Heteroaromatics in Water
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Sonogashira Couplings of Aryl Bromides: Room Temperature, Water Only, No Copper
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started