e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Chemical Communications
Palladium-catalysed N-annulation routes to indoles: the synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1
AJ Fletcher, MN Bax, MC Willis
Index: Fletcher, Anthony J.; Bax, Matthew N.; Willis, Michael C. Chemical Communications, 2007 , # 45 p. 4764 - 4766
The majority of indole syntheses involve cyclisation of an acyclic precursor that contains the key N-atom. To adapt these syntheses to the preparation of N-substituted indoles requires that either the precursors must be modified (to include the substituent), or an efficient and selective functionalisation of an indole N–H must be achieved. This is often problematic; for example, syntheses of the simple natural product 1, and related structures, resort to functionalisation of indoline derivatives ...