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Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 15, pp. 3868 - 3871
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 07/2014, Volume 20, Issue 31, pp. 9739 - 9743
Site‐selective ruthenium(II)‐catalyzed direct arylation of amides was achieved through CH cleavages with modular auxiliaries, derived from easily accessible... 
triazoles | ruthenium | catalysis | CH activation | amides | aryl halides | C-H activation | DIRECTING GROUP | C(SP)-H BONDS | ACTIVATION | DIRECT FUNCTIONALIZATION | CLICK CHEMISTRY | CHEMISTRY, MULTIDISCIPLINARY | BIDENTATE-CHELATION ASSISTANCE | UNACTIVATED C(SP)-H BONDS | ACID-DERIVATIVES | INTRAMOLECULAR AMINATION | ARYL CHLORIDES | Alkenes | Accessibility | Aromatic compounds | Amides | Strategy | Cleavage | Activation | Modular
Journal Article
Tetrahedron, ISSN 0040-4020, 02/2020, Volume 76, Issue 9, p. 130925
Journal Article
Organic Letters, ISSN 1523-7060, 10/2017, Volume 19, Issue 19, pp. 5458 - 5461
We report here a manganese-catalyzed C–H methylation reaction of considerable substrate scope, using MeMgBr, a catalytic amount of MnCl2·2LiCl, and an organic... 
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 42, pp. 5354 - 5356
The presence of a bromide substituent, instead of a hydrogen or methyl group, on a carbon-carbon double bond, protects the alkene from addition reactions when... 
TARTARIC ACID | ALKYLATION | ESTERS | BONDS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | ZARAGOZIC ACIDS | Cross coupling | Synthesis | Alkenes | Carbon | Substrates
Journal Article
Beilstein journal of organic chemistry, ISSN 1860-5397, 2019, Volume 15, Issue 1, pp. 1194 - 1202
( , )-Dimethyl tartrate acetonide in THF/HMPA undergoes deprotonation with LDA and reaction at -78 °C during 12-72 h with a range of alkyl halides, including... 
Studies | Chemistry | Acids | Asymmetric synthesis | Natural products | Oxidation | Tartaric acid | Alkylation | Carbonyls | alkylation | diazoester | cycloaddition | tartaric acid | epimerisation
Journal Article
Molbank, ISSN 1422-8599, 07/2019, Volume 2019, Issue 3, p. M1075
The title compound, N-benzo[c][1,2,5]thiazol-4-yl-3-trifluoromethylbenzamide (1) was synthesized by reacting 3-trifluoromethylbenzoyl chloride (4) and... 
benzamide | C-H functionalization | bidentate directing group
Journal Article
Organic Letters, ISSN 1523-7060, 07/2017, Volume 19, Issue 13, pp. 3540 - 3543
An asymmetric synthesis of (−)-6,7-dideoxysqualestatin H5 is reported. Key features of the synthesis include the following: (1) highly diastereoselective... 
SQUALENE SYNTHASE INHIBITOR | 6,7-DIDEOXYSQUALESTATIN H5 | TARTARIC ACID | ZARAGOZIC ACID-C | DOUBLE-BONDS | ALKYLATION | BIOSYNTHESIS | ESTERS | SQUALESTATINS | CHEMISTRY, ORGANIC | STRUCTURE ELUCIDATION
Journal Article
Molbank, ISSN 1422-8599, 12/2019, Volume 2020, Issue 1, p. M1099
The title compound, N-(2-hydroxy-1,1-dimethylethyl)-3-methylbenzamide was synthesized by reacting 3-methylbenzoyl chloride or 3-methylbenzoic acid with... 
Journal Article
Organic Letters, ISSN 1523-7060, 09/2018, Volume 20, Issue 17, pp. 5528 - 5528
Journal Article
Chemistry of Heterocyclic Compounds, ISSN 0009-3122, 3/2018, Volume 54, Issue 3, pp. 214 - 240
In the last decade, metal-catalyzed [3+2] cycloadditions of azomethine imines have emerged as a regioselective and stereoselective method for the synthesis of... 
Chemistry | Pharmacy | azomethine imines | [3+2] cycloadditions | pyrazolines | transition metals | catalysis | cyclization | Organic Chemistry | ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION | LEWIS-ACID | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | PEPTIDE MIMETICS | COPPER | SILVER TRIFLATE | ETHYL PROPIOLATE | SIMPLE-MODEL | MANZACIDIN-C | TANDEM REACTION | Schiff bases
Journal Article
ISSN 1359-7345, 5/2018, Volume 54, Issue 42, pp. 5354 - 5356
The presence of a bromide substituent, instead of a hydrogen or methyl group, on a carbon-carbon double bond, protects the alkene from addition reactions when... 
Journal Article
Angewandte Chemie, ISSN 0044-8249, 04/2014, Volume 126, Issue 15, pp. 3949 - 3952
Modulare 1,2,3‐Triazole ermöglichten Eisen‐katalysierte C‐H‐Arylierungen mit hoher Anwendungsbreite. Das neuartige Triazol‐basierte, zweizähnige Auxiliar ist... 
Triazole | Ruthenium | C‐H‐Aktivierung | Eisen | Chelate
Journal Article
Angewandte Chemie, ISSN 0044-8249, 04/2014, Volume 126, Issue 15, pp. 3949 - 3952
Modulare 1,2,3-Triazole ermöglichten Eisen-katalysierte C-H-Arylierungen mit hoher Anwendungsbreite. Das neuartige Triazol-basierte, zweizähnige Auxiliar ist... 
Journal Article
ChemInform, ISSN 0931-7597, 02/2015, Volume 46, Issue 7, pp. no - no
The direct arylation of amides is investigated in the presence of different side chain modifications and the triazole‐based auxiliary ‐NH‐Tam is found to be... 
carboxylic amides (benzene compounds) | polyphenyl derivatives | C‐C bond formation | Triazoles | Amides | Ruthenium
Journal Article
ChemInform, ISSN 0931-7597, 09/2014, Volume 45, Issue 36, pp. no - no
This method utilizes a triazole‐derived auxiliary for the iron‐catalyzed activation of otherwise inert C(sp2)—H and C(sp3)—H bonds. 
carboxylic amides (benzene compounds) | catalysis, phase‐transfer catalysis | carboxylic amides (acyclic compounds) | polyphenyl derivatives | C‐C bond formation | Triazoles | Catalysis
Journal Article