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Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2019, Volume 361, Issue 3, pp. 469 - 475
A regioselective method to access fully substituted 5‐trifluoromethylthio‐1,2,3‐triazoles and 5‐thio‐1,2,3‐triazoles from the internal alkynyl trifluoromethyl... 
regioselectivity | 5-trifluoromethylthio-1,2,3-triazoles | 5-thio-1,2,3-triazoles | mild conditions | rhodium | DRUG | FIPRONIL | REAGENTS | CLICK CHEMISTRY | COCCIDIOSIS | TOLTRAZURIL | CHEMISTRY, ORGANIC | 1,2,3-TRIAZOLES | ALPHA-FLUORINATED ETHERS | CHEMISTRY, APPLIED | CEFAZAFLUR | THIOETHERS | Cycloaddition | Rhodium | Regioselectivity | Triazoles | Chemical synthesis | Functional groups | Substrates | Alkynes
Journal Article
Organic Letters, ISSN 1523-7060, 08/2009, Volume 11, Issue 15, pp. 3430 - 3433
A stereoselective intramolecular normal demand [4 + 2] cycloaddition of allenamides under thermal conditions without metal assistance is described. This work... 
REARRANGEMENT | DIENES | ENTRY | GOLD CATALYSIS | STABILIZED OXYALLYL CATIONS | PLATINUM | CHEMISTRY, ORGANIC | ALLENES | ALKYNES | ACCESS
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 2010, Volume 39, Issue 5, pp. 1467 - 1477
Cycloaddition reactions belong to one of the most well-investigated and widely used reactions in synthetic organic chemistry for the construction of (hetero)... 
CORE | 1,3-DIPOLAR CYCLOADDITIONS | AZIDES | ANALOG | PINNAIC ACID | CLICK CHEMISTRY | TERMINAL ALKYNES | CASCADE | TIAZOFURIN | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 08/2010, Volume 132, Issue 32, pp. 11039 - 11041
A formal, metal-free, [2 + 2 + 2] cycloaddition strategy is described based on a cascade of two pericyclic processes. The first step involves an intramolecular... 
ORGANIC-SYNTHESIS | CYCLOTRIMERIZATION | ALKYNES | ALLENES | CHEMISTRY, MULTIDISCIPLINARY | COMPLEXES | Substrate Specificity | Alkenes - chemistry | Alkynes - chemistry | Cyclization | Stereoisomerism | Chemical properties | Diels-Alder reaction | Structure | Olefins | Analysis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2009, Volume 48, Issue 52, pp. 9879 - 9883
How to click with biomolecules: Copper‐catalyzed azide–alkyne cycloaddition has been optimized for use with biological molecules. The key development is the... 
bioconjugation | copper | cycloaddition | azides | alkynes | Azides | Cycloaddition | Bioconjugation | Copper | Alkynes | VIRUS | ACID | ASCORBATE OXIDATION | CLICK CHEMISTRY | LIGATION | CHEMISTRY, MULTIDISCIPLINARY | LIGANDS | DNA | PROTEINS | Copper - chemistry | Ascorbic Acid - chemistry | Allolevivirus - chemistry | Serum Albumin, Bovine - chemistry | Alkynes - chemistry | Catalysis | RNA - chemistry | Azides - chemistry
Journal Article
Angewandte Chemie - International Edition, ISSN 0570-0833, 2009, Volume 48, Issue 27, pp. 4900 - 4908
Journal Article
Organic Letters, ISSN 1523-7060, 12/2016, Volume 18, Issue 23, pp. 6034 - 6037
The domino reactions between NH-based secondary enaminones and tosyl azide have been developed for the synthesis of various N-substituted 1,2,3-triazoles by... 
SODIUM-AZIDE | CLICK CHEMISTRY | 1,3-DIPOLAR CYCLOADDITION | REGIOSELECTIVE SYNTHESIS | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | TERMINAL ALKYNES | ORGANIC AZIDES | METAL-FREE | ALKYNE CYCLOADDITION
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 37, pp. 9865 - 9869
Journal Article