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Chemistry – A European Journal, ISSN 0947-6539, 07/2019, Volume 25, Issue 40, pp. 9433 - 9437
Journal Article
Angewandte Chemie - International Edition, ISSN 1433-7851, 2016
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2019
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2019, Volume 58, Issue 19, pp. 6225 - 6229
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2015, Volume 21, Issue 35, pp. 12303 - 12307
An intramolecular domino process consisting of a formal anti ‐carbopalladation followed by Heck reaction is realized. Complex oligo(hetero)cyclic scaffolds are... 
Heck reaction | palladium | heterocycles | carbopalladation | domino reaction | ROUTE | ALKENYL HALIDES | MECHANISM | PALLADIUM-CATALYZED CYCLIZATION | COMPLEXES | STEREOCHEMISTRY | ALKYNES | TRANS | CHEMISTRY, MULTIDISCIPLINARY | CASCADE CYCLIZATION | ISOCHROMANS | Substitution reactions | Palladium | Chemical properties | Hydrogen | Residues | Accessibility | Precursors | Catalysis | Scaffolds | Bonding | Alkynes
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 09/2019, Volume 25, Issue 50, pp. 11620 - 11624
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 7, pp. 1955 - 1959
Journal Article
Organic Letters, ISSN 1523-7060, 2018, Volume 20, Issue 22, pp. 7266 - 7269
An intramolecular cascade reaction consisting of a formal anti-carbopalladation terminated by the ring opening of a cyclopropanol unit is presented. The... 
CHROMANS | ROUTE | AMINATION | MECHANISTIC INSIGHTS | BONDS | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | DOMINO APPROACH | HELICENES | ACCESS | ISOCHROMANS
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 10/2016, Volume 22, Issue 41, pp. 14544 - 14547
An intramolecular Pd‐catalyzed trans ‐dicarbofunctionalization of internal alkynes using aryl bromides and aryl stannanes is presented. Tetrasubstituted double... 
Stille reaction | carbopalladation | domino reaction | alkynes | dicarbo functionalization | CHROMANS | DOMINO REACTIONS | EFFICIENT ROUTE | TETRASUBSTITUTED ALKENES | MOLECULAR SWITCHES | HELICENES | CHEMISTRY, MULTIDISCIPLINARY | ARYL CHLORIDES | ACCESS | ISOCHROMANS | CYCLIZATION | Residues | Embedded systems | Aromatic compounds | Cascades | Chemical bonds | Transformations | Tolerances | Alkynes
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2019, Volume 25, Issue 44, pp. 10323 - 10327
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 31-32, pp. 5254 - 5260
The reactivity of 3,3′‐linked bispyrroles, easily accessible by ring‐enlargement reactions of donor–acceptor cyclopropanes, towards various carbon... 
Heterocycles | Aromatic systems | Bispyrroles | Pyrroles | Donor–acceptor cyclopropanes | ONE-POT | AZOMETHINE YLIDES | CHEMISTRY, ORGANIC | Donor-acceptor cyclopropanes | AZIDES SYNTHESIS | SUBSTITUTED CYCLOPROPANES | 3+2 ANNULATION | 1,3-DIPOLAR CYCLOADDITION | RING-ENLARGEMENT | OLIGOPYRROLE SYNTHESIS | ACCESS | Schiff bases
Journal Article
Synlett, ISSN 0936-5214, 07/2019, Volume 30, Issue 11, pp. 1275 - 1288
Abstract Our endeavors in the design, realization and application of a formal anti -carbopalladation of alkynes are summarized. Whereas numerous examples of... 
account | mechanistic studies | lysergol | cascade | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | PALLADIUM-CATALYZED REACTION | ALKYNES | carbopalladation | anti | DOMINO ACCESS | ALKENES | heterocycles | MECHANISTIC INSIGHTS | CONSTRUCTION | CYCLOCARBOPALLADATION | reaction design | palladium | ARYL IODIDES | domino reaction | CYCLIZATION
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 04/2012, Volume 134, Issue 15, pp. 6544 - 6547
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2015, Volume 54, Issue 13, pp. 4119 - 4123
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 08/2019, Volume 21, Issue 16, pp. 6315 - 6319
Donor-acceptor (D-A) cyclobutanes with two geminal ester groups as acceptors are reacted with electron-rich arenes as nucleophiles to afford ring-opened... 
3+2 ANNULATION | ACID | PYRROLIDINES | STRATEGY | CONSTRUCTION | FORMAL 4+2 CYCLOADDITION | REACTIVITY | CHEMISTRY, ORGANIC | GENERATION | SUBSTITUTED CYCLOPROPANE | DERIVATIVES
Journal Article