Synthesis of Carbazoles from Ynamides by Intramolecular Dehydro Diels−Alder Reactions
Organic Letters2005Vol. 7(11), pp. 2213–2216
Citations Over TimeTop 10% of 2005 papers
Abstract
[reaction: see text]. A new approach to carbazoles and benzannulated carbazoles by means of intramolecular dehydro Diels-Alder reactions of ynamides is reported. By using this approach, carbazoles and benzo[b]-, tetrahydrobenzo[b]-, naphtho[1,2-b]-, naphtho[2,1-b]-, and dibenzo[a,c]carbazoles have been prepared in moderate-to-good yields.
Related Papers
- → Intramolecular Diels–Alder Reaction of Vinylsulfonic Acid Esters(1989)44 cited
- → Intramolecular isotope effects in the reactions of CF32+ and CO22+ with HD(2001)28 cited
- → Nature of weak inter-and intramolecular interactions in crystals 8. Influence of intermolecular contacts on the strength of intramolecular O-H...N bonds in crystals of 3-(2-hydroxyphenyl)-1,2,4-triazoles(2006)3 cited
- → Stimulation intramolecular F⋯H hydrogen bond by intramolecular N → Si interaction in Si-fluoro derivatives of 8-mercaptoquinoline: DFT and MP2 calculations(2018)1 cited
- → ChemInform Abstract: Inter‐ and Intramolecular Hetero‐Diels‐Alder Reactions. Part 29. Synthesis of Enantiomerically Pure Heterosteroids by Intramolecular Hetero‐Diels‐Alder Reaction.(1990)2 cited