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ACS Catalysis, ISSN 2155-5435, 09/2017, Volume 7, Issue 9, pp. 5618 - 5627
The indole scaffold will continue to play a vital part in the future of drug discovery and agrochemical development. Because of this, the necessity for elegant... 
regioselectivity | heteroaromatics | indole | homogeneous catalysis | C-H functionalization | DIRECTING GROUP | ROOM-TEMPERATURE | 7-SUBSTITUTED INDOLES | NATURAL-PRODUCTS | BOND FUNCTIONALIZATIONS | CHEMISTRY, PHYSICAL | INTERNAL ALKYNES | MILD CONDITIONS | RUTHENIUM CATALYSIS | REGIOSELECTIVE SYNTHESIS | 2,3-DISUBSTITUTED INDOLES
Journal Article
ACS Catalysis, ISSN 2155-5435, 04/2017, Volume 7, Issue 4, pp. 2616 - 2623
The site-selective functionalization of an indole template offers exciting possibilities for the derivatization of molecules with useful biological properties.... 
heteroaromatics | ruthenium | indole | homogeneous catalysis | remote functionalization
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2017, Volume 56, Issue 47, pp. 15131 - 15135
The para‐selective C−H alkylation of aniline derivatives furnished with a pyrimidine auxiliary is herein reported. This reaction is proposed to take place via... 
reaction mechanisms | ruthenium | C−H activation | arenes | homogeneous catalysis | ENANTIOSELECTIVE DEAROMATIZATION | ACID | SPIROINDOLENINES | IRIDIUM | STEREOSELECTIVE MIGRATION | CHEMISTRY, MULTIDISCIPLINARY | DESYMMETRIZATION | ASYMMETRIC ALLYLIC SUBSTITUTIONS | C-H activation | DEAROMATIZATION REACTIONS | CARBON-CARBON | INDOLE ALKALOIDS | Aniline | Ruthenium | Catalysis | Derivatives | Catalysts | Alkylation
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2017, Volume 53, Issue 97, pp. 13039 - 13042
We report the C4-selective C–H alkylation of carbazole derivatives furnished with a pyrimidine directing group at N9. This was realized using ruthenium... 
Carbazoles | Activation | Ruthenium | Alkylation
Journal Article
Chemical Communications, ISSN 1359-7345, 2017, Volume 53, Issue 97, pp. 13039 - 13042
We report the C4-selective C-H alkylation of carbazole derivatives furnished with a pyrimidine directing group at N9. This was realized using ruthenium... 
Journal Article
ISSN 1359-7345, 12/2017, Volume 53, Issue 97, pp. 1339 - 1342
We report the C4-selective C-H alkylation of carbazole derivatives furnished with a pyrimidine directing group at N9. This was realized using ruthenium... 
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2016, Volume 81, Issue 20, pp. 10081 - 10087
Ruthenium­(II)-catalyzed C–H functionalization of N-arylhydantoins is herein described. The biologically relevant hydantoin (imidazolidinedione) heterocycle... 
CHEMISTRY, ORGANIC | ACTIVATED ALKENES | BOND ACTIVATION | DERIVATIVES | CATALYZED ORTHO-ALKENYLATION | PROSTATE-CANCER
Journal Article
Angewandte Chemie, ISSN 0044-8249, 11/2017, Volume 129, Issue 47, pp. 15327 - 15331
The para‐selective C−H alkylation of aniline derivatives furnished with a pyrimidine auxiliary is herein reported. This reaction is proposed to take place via... 
Arene | Homogene Katalyse | Ruthenium | Reaktionsmechanismen | C-H-Aktivierung | Aniline
Journal Article
ACS Catalysis, ISSN 2155-5435, 08/2016, Volume 6, Issue 8, pp. 5520 - 5529
Herein, we report the ruthenium-catalyzed ortho C–H alkenylation of a wide range of N-aryloxazolidinone scaffolds. Alkenylation was achieved with complete... 
ruthenium | kinetic isotope effect | C-H activation | DFT | homogeneous catalysis | heterocycles | AROMATIC KETONES | DIRECT ORTHO ARYLATION | N-ARYLOXAZOLIDINONES | CHEMISTRY, PHYSICAL | ANTITHROMBOTIC AGENT | DISCOVERY | ALKENES | CATALYZED ORTHO-ALKENYLATION | BOND ACTIVATION
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 07/2009, Volume 74, Issue 14, p. 5041
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 07/2009, Volume 74, Issue 14, pp. 5041 - 5048
7-Azabicyclo[2.2.1]heptane-2-carboxylic acid 11 was prepared in enantiopure form, and its catalytic potential in the direct aldol reaction between acetone and... 
DENSITY | CATALYSIS | POLARIZABLE CONTINUUM MODEL | MECHANISM | MANNICH-TYPE REACTIONS | AMINO ACIDS | CHEMISTRY, ORGANIC | ASYMMETRIC ORGANOCATALYSIS | ALDEHYDES | TRANSITION-STATES | SAUER-WIECHERT REACTION | Proline - analogs & derivatives | Stereoisomerism | Molecular Structure | Catalysis | Aldehydes - chemistry | Hydrogen-Ion Concentration | Proline - chemistry
Journal Article
Angewandte Chemie, ISSN 0044-8249, 11/2017, Volume 129, Issue 47, p. 15327
The para-selective C-H alkylation of aniline derivatives furnished with a pyrimidine auxiliary is herein reported. This reaction is proposed to take place via... 
Ruthenium | Aniline | Catalysts | Catalysis | Derivatives | Alkylation
Journal Article
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