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Data · dataset · 2026

Raw data for "Unlocking the Potential of Organoaluminum Reagents for Versatile C–C Couplings Using YPhos-Pd Catalysts"

Listed in TUDOdata

PROJECT DESCRIPTION: We report a general and efficient protocol for the palladium-catalyzed cross-coupling of aryl chlorides with a broad range of organoaluminum nucleophiles, enabled by strongly donating ylide-functionalized phosphines (YPhos).

Description

Unlike other earth-abundant organometallic reagents, the protocol demonstrates broad functional group tolerance, even allowing for late-stage functionalizations of complex molecules.

In general, high selectivities and yields are achieved, while maintain-ing the high reactivity characteristics of this class of compounds even at room temperature. The presented protocol high-lights the key advantages of this thus far underestimated class of nucleophiles in coupling chemistry and illustrates both the strengths and limitations of in situ generated alkyl-, aryl-, alkenyl-, and alkynylaluminum reagents. DATASET DESCRIPTION: Single folders were created for all experiment types (NMR, IR, HRMS, GC-MS) for isolated compounds.

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Within those folders, subfolders for the five different scopes were created with the related data within those folders. The names of the data files are in accordance with the electronic-laboratory-journal (ELN) used in the Gessner-Group. The Excel file "Data Repository Guide" shows the conncection of the scope molecule number of the publication and the data file names.

Programs that can be used to open the data: IR: The data can be opened with OMNIC software (an open source alternative would be the software "OpenChrom"). NMR: Can be opened with MestReNova. HRMS: PDF file with spectra were provided.

GC: Can be opened with Masshunter Qualitative Analysis.

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Where it is published

Catalogue records · 1

Topics

Stated by source
Chemistry
Inferred from text
Physical chemistry 75%
Provenance · 1 source records, 13 field assertions
SourceKeyLast seenRaw
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