Iterative C-H Functionalization Leading to Multiple Amidations of Anilides

Cited 67 time in webofscience Cited 0 time in scopus
  • Hit : 456
  • Download : 0
Polyaminobenzenes were synthesized by the ruthenium-catalyzed iterative C-H amidation of anilides using dioxazolones as an amino source. This strategy could be implemented by the sequential activation of C-H bonds of formerly generated compounds by cascade chelation assistance of newly installed amide groups. Computational studies provided a rationale.
Publisher
WILEY-V C H VERLAG GMBH
Issue Date
2017-04
Language
English
Article Type
Article
Keywords

CATALYZED 4+2 BENZANNULATION; AROMATIC-COMPOUNDS; BOND ACTIVATION; NITROGEN-SOURCE; CHELATION ASSISTANCE; SULFONYL AZIDES; AMIDO TRANSFER; ARENES; AMINATION; DERIVATIVES

Citation

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.15, pp.4256 - 4260

ISSN
1433-7851
DOI
10.1002/anie.201701138
URI
http://hdl.handle.net/10203/223222
Appears in Collection
CH-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 67 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0