Overcoming the limitations of directed C–H functionalizations of heterocycles
Overcoming the limitations of directed C–H functionalizations of heterocycles
About this item
Full title
Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
Formats
Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
A robust and synthetically useful method is reported that overcomes the complications associated with performing C–H functionalization reactions on heterocycles; a reactive PdX
2
(X = ArCONOMe) species is generated
in situ
, and is directed to the appropriate C–H bond by an
N
-methoxy amide group.
Heterocycle poisoning bypassed...
Alternative Titles
Full title
Overcoming the limitations of directed C–H functionalizations of heterocycles
Authors, Artists and Contributors
Author / Creator
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_1629594633
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1629594633
Other Identifiers
ISSN
0028-0836
E-ISSN
1476-4687
DOI
10.1038/nature13885
