Nitrogen–boron coordination versus OH⋯N hydrogen bonding in pyridoxaboroles – aza analogues of benzoxaboroles-Reference-Cited by-同舟云学术

Nitrogen–boron coordination versus OH⋯N hydrogen bonding in pyridoxaboroles – aza analogues of benzoxaboroles

Published:2015 Issue:37 Volume:44 Page:16534-16546
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Steciuk I.¹²³⁴⁵,Durka K.¹²³⁴⁵,Gontarczyk K.¹²³⁴⁵,Dąbrowski M.¹²³⁴⁵,Luliński S.¹²³⁴⁵,Woźniak K.⁶⁷⁸⁵

Affiliation:

1. Warsaw University of Technology

2. Faculty of Chemistry

3. Physical Chemistry Department

4. 00-664 Warsaw

5. Poland

6. University of Warsaw

7. Department of Chemistry

8. 02-093 Warsaw

Abstract

Pyridoxaboroles are novel amphoteric heterocycles forming either hydrogen-bonded networks or polymeric aggregates depending on the donor properties of a nitrogen atom.

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/DT/C5DT02402A

Reference92 articles.

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3. The synthesis of benzoxaboroles and their applications in medicinal chemistry

4. The unique chemistry of benzoxaboroles: Current and emerging applications in biotechnology and therapeutic treatments

5. Recent Developments in the Chemistry and Biological Applications of Benzoxaboroles

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