Abstract
The intramolecular dehydro-Diels-Alder reaction of 1-indolyl-1,6-heptadiynes proceeds smoothly under rather mild heating conditions to give substituted carbazoles in moderate to good yields. The reaction of 7-aryl-1-indolyl-1,6-heptadiynes under heating gives the corresponding carbazoles chemoselectively in high yields, whereas the reaction under basic conditions gives naphthalenes as major products.
Original language | English |
---|---|
Pages (from-to) | 2189-2193 |
Number of pages | 5 |
Journal | Synlett |
Volume | 28 |
Issue number | 16 |
DOIs | |
Publication status | Published - 2017 |
Keywords
- carbazoles
- chemoselectivity
- dehydro-Diels-Alder reaction
- indoles
- intramolecular Diels-Alder reaction
- naphthalenes
ASJC Scopus subject areas
- Organic Chemistry