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Cited by 244

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Improved Ruthenium‐Catalyzed Amination of Alcohols with Ammonia: Synthesis of Diamines and Amino Esters

Imm, Sebastian, Bähn, Sebastian, Zhang, Min, Neubert, Lorenz, Neumann, Helfried, Klasovsky, Florian, Pfeffer, Jan, Haas, Thomas, Beller, Matthias·2011·Angewandte Chemie International Edition

Abstract

Diamination of diols: The first homogeneously catalyzed diaminations of primary and secondary diols with ammonia give the corresponding diamines. Other primary as well as secondary alcohols including hydroxy-substituted esters can also be efficiently converted to primary amines. This atom-efficient and selective amination method proceeds in an ammonia atmosphere without additional hydrogen sources.

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Crossref · 10.1002/anie.201103199

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Metadata

Authors
Imm, S., Bähn, S., Zhang, M., Neubert, L., Neumann, H., Klasovsky, F., Pfeffer, J., Haas, T., & Beller, M.
Venue
Angewandte Chemie International Edition
Publisher
Wiley
Published
2011-07-05
Volume
50
Issue
33
Pages
7599-7603
ISSN
  • 1433-7851 (ISSN-L)
  • 1521-3773
OpenAlex
W1977420451
Cited by
244
References
1
FWCI
13.31
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Improved Ruthenium‐Catalyzed Amination of Alcohols with Ammonia: Synthesis of Diamines and Amino Esters. https://app.cochat.ai/papers/10.1002/anie.201103199
The paper
Imm, S., Bähn, S., Zhang, M., Neubert, L., Neumann, H., Klasovsky, F., Pfeffer, J., Haas, T., & Beller, M. (2011). Improved Ruthenium‐Catalyzed Amination of Alcohols with Ammonia: Synthesis of Diamines and Amino Esters. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201103199

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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