One-pot synthesis of new substituted 1,2,3,4-tetrahydrocarbazoles via Petasis reaction.

The one-pot synthesis of a new substituted 1,2,3,4-tetrahydrocarbazoles has been described via Petasis reactions. These tetrahydrocarbazoles exhibits various medicinal importance and might be suitable for elaboration into larger peptides at carboxy termini. The scope and limitations of this method have been examined.