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Number of results

Journal

2011 | 9 | 2 | 199-205

Article title

Amination-reduction reaction as simple protocol for potential boronic molecular receptors. Insight in supramolecular structure directed by weak interactions

Content

Title variants

Languages of publication

EN

Abstracts

EN
The synthesis of the potential molecular receptors in the amination-reduction reaction has been investigated within the model system comprising (2-formylphenyl)boronic acid and morpholine. The 3-amine substituted benzoxaborole was identified to be the intermediate of the synthesis and the unsubstituted benzoxaborole as the by-product resulting from reduction of the starting material. The insight into the reactivity of the starting materials as well as the intermediate benzoxaborole enabled significant rise in the yield of 2-(aminomethyl) phenylboronic acids synthesis. The solid state structure of 2-(piperidylmethyl)phenylboronic acid has been re-determined, and the description of the molecule and the crystal is given. The supramolecular layer structure directed by the weak C-H…O and C-H…π interactions was identified and scrutinized based on the geometry and Hirshfeld surface analyses

Publisher

Journal

Year

Volume

9

Issue

2

Pages

199-205

Physical description

Dates

published
1 - 4 - 2011
online
17 - 2 - 2011

Contributors

  • Warsaw University of Technology
  • Warsaw University of Technology
  • Warsaw University of Technology
  • Warsaw University of Technology
  • Warsaw University of Technology
author
  • Warsaw University of Technology

References

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Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11532-010-0142-8
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