This title appears in the Scientific Report :
2012
Please use the identifier:
http://dx.doi.org/10.1039/C2DT30502J in citations.
A regioselective Huisgen reaction inside a Keplerate polyoxomolybdate nanoreactor
A regioselective Huisgen reaction inside a Keplerate polyoxomolybdate nanoreactor
A 1,3-dipolar cycloaddition reaction taking place quantitatively between propiolic acid "guests" and azide functions previously attached to binding sites within the cavity of a {Mo(132)}-type Keplerate reproducibly gives a 2 : 1 ratio of 1,4- and 1,5-triazoles.
Saved in:
Personal Name(s): | Besson, C. |
---|---|
Schmitz, S. / Capella, K.M. / Kopilevich, S. / Weinstock, I.A. / Kögerler, P. | |
Contributing Institute: |
Elektronische Eigenschaften; PGI-6 |
Published in: | Dalton transactions, 41 (2012) S. 9852 - 9854 |
Imprint: |
London
Soc.
2012
|
Physical Description: |
9852 - 9854 |
DOI: |
10.1039/C2DT30502J |
PubMed ID: |
22782444 |
Document Type: |
Journal Article |
Research Program: |
Grundlagen für zukünftige Informationstechnologien |
Series Title: |
Dalton Transactions
41 |
Subject (ZB): | |
Publikationsportal JuSER |
A 1,3-dipolar cycloaddition reaction taking place quantitatively between propiolic acid "guests" and azide functions previously attached to binding sites within the cavity of a {Mo(132)}-type Keplerate reproducibly gives a 2 : 1 ratio of 1,4- and 1,5-triazoles. |