New strategies for chemical synthesis : 1) Development of a palladium-catalyzed direct C-H alkenylation of indoles by solvent-controlled regioselective C-H bond functionalisation; 2) Studies towards the development of a catalytic diastereoselective [3,3] sigmatropic rearrangement at ambient temperature
Main Author: | Grimster, Neil Patrick |
---|---|
Published: |
University of Cambridge
2007
|
Subjects: | |
Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.612869 |
Similar Items
-
Synthesis of 3-alkenylindoles through regioselective C–H alkenylation of indoles by a ruthenium nanocatalyst
by: Abhijit Paul, et al.
Published: (2020-01-01) -
Palladium-catalyzed mono- and di-alkenylation of N-acetyl-2-aminobiaryls via regioselective C-H bond activation
by: Hsu, Kao-Chi, et al.
Published: (2016) -
Enantioselective C(sp3)-H Arylation and Development of a Modular C(sp3)-H Alkenylation
by: Holstein, Philipp
Published: (2014) -
Stereochemistry of [2,3] and [3,3] sigmatropic rearrangements
by: Yamamoto, Yukio
Published: (2009) -
Palladium Catalysed C-H Functionalisation of Aryl Ureas
by: Houlden, Christopher
Published: (2009)