17017-59-3Relevant articles and documents
Palladium-catalysed dehydrogenative generation of imines from amines. A nature-inspired route to indoles via cross-couplings of amines with arylhydrazines
Taddei, Maurizio,Mura, Manuel G.,Rajam?ki, Suvi,De Luca, Lidia,Porcheddu, Andrea
, p. 3002 - 3013 (2014/03/21)
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. However, this class of molecules can be prepared through selective removal of a hydrogen molecule from a primary amine using a transition metal catalyst. This biomimetic transformation, previously employed for the N-alkylation of anilines, is applied here to a domino preparation of differently substituted indoles from aliphatic primary amines and arylhydrazines. Several different linear and branched aliphatic primary amines are oxidized with reusable palladium on charcoal to the corresponding primary imines entrapped as arylhydrazones that can be isolated as such. Arylhydrazones can be further converted into N-alkylindole derivatives via an acid-mediated indolisation reaction. The one-pot domino hydrogen transfer Fischer indole synthesis under heterogeneous catalysis is also possible, giving access to diverse substituted indoles, including NH indoles obtained after deprotection of the corresponding benzyl compounds. The truly heterogeneous nature of the catalyst was demonstrated by recycling the catalyst in the same reaction, and in other palladium-catalysed transformations.
An Expeditious Synthesis of 3-Alkyl-, Aryl- and Heteroaryl-indoles by way of an Intramolecular Horner-Wittig Reaction
Couture, Axel,Deniau, Eric,Gimbert, Yves,Grandclaudon, Pierre
, p. 2463 - 2466 (2007/10/02)
A variety of 3-alkyl-, aryl- and heteroaryl-indoles have been efficiently prepared by base-induced intramolecular cyclization of suitable aromatic o-acyl substituted Horner-Wittig reagents.
