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Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2017, Volume 56, Issue 26, pp. 7420 - 7424
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2019, Volume 58, Issue 19, pp. 6396 - 6399
We describe the design and application of tailored aminoallyl precursors for catalytic (3+2... 
palladium | (3+2) cycloaddition | aminoallyl | pyrrolidines | dienes | Palladium catalysts | Palladium | Cycloaddition | Selectivity | Catalysis | Pyrrolidine | Dienes | Index Medicus
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 07/2013, Volume 355, Issue 10, pp. 1948 - 1954
The reaction of nitriles with alkenyldiazo compounds in the presence of gold catalysts provides functionalized pyrrole derivatives in moderate to high yields. This formal [3+2... 
[3+2] cyclization | nitriles | gold catalysis | diazo compounds | pyrroles | [3+2] cyclization | Diazo compounds | Nitriles | Synthesis | Pyrroles | Terminals | Derivatives | Catalysis | Compatibility | Bearing
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 11/2014, Volume 356, Issue 16, pp. 3363 - 3369
...‐diaryl moiety through a thermal intramolecular [2+2] cycloaddition approach. By using the same approach, bicyclo[3.1.1]heptane, 3‐azabicyclo[3.2.0]heptane, and 3‐oxabicyclo[3.1.1... 
intramolecular [2+2] cycloaddition | 3‐azabicyclo[3.2.0]heptanes | Morita–Baylis–Hillman adducts | 3‐azabicyclo[3.1.1]heptanes | Morita-Baylis-Hillman adducts | 3-azabicyclo[3.1.1]heptanes | Intramolecular [2+2] cyclo-addition | 3-aza-bicyclo[3.2.0]heptanes | Bisphenol-A | Synthesis | Derivatives | Catalysis | Bearing
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2014, Volume 53, Issue 28, pp. 7209 - 7213
...‐Dialkylthio cyclopentadienes were prepared by the BF3⋅Et2O catalyzed regiospecific [3+2] cycloaddition of propargylic alcohols and α... 
ketene dithioacetals | cyclopentadienes | propargylic alcohols | [3+2] cycloaddition | Diels–Alder reaction | Diels-Alder reaction
Journal Article
Chemistry, an Asian journal, ISSN 1861-4728, 04/2018, Volume 13, Issue 8, pp. 959 - 963
Diastereo‐ and enantioselective cycloaddition of 3‐nitroindoles with vinyl aziridine was realized under Pd... 
palladium | nitroindoles | asymmetric catalysis | [3+2] cycloaddition | dearomatization | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Enantiomers | Palladium | Catalysis
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2018, Volume 57, Issue 39, pp. 12916 - 12920
A protocol for the asymmetric synthesis of highly substituted chiral allenes with control of point and axial chirality has been developed. A palladium‐catalyzed [3+2... 
asymmetric catalysis | chiral allenes | reaction mechanism | [3+2] cycloaddition | DYKAT | Palladium | Synthesis | Catalysis | Organic compounds | Stereoselectivity | Cycloaddition | Asymmetry | Asymmetric synthesis | Allene | Chirality | Chemical reactions | Chemical synthesis | Functional groups
Journal Article