A Highly Efficient and Flexible Synthesis of Substituted Carbazoles by Rhodium-Catalyzed Inter- and Intramolecular Alkyne Cyclotrimerizations
- 30 August 2002
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 41 (17) , 3281-3284
- https://doi.org/10.1002/1521-3773(20020902)41:17<3281::aid-anie3281>3.0.co;2-g
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- New and Efficient Synthesis of Stannyl EnaminesSynthesis, 2001
- Chemo- and regioselective crossed alkyne cyclotrimerisation of 1,6-diynes with terminal monoalkynes mediated by Grubbs’ catalyst or Wilkinson’s catalystChemical Communications, 2000
- Rhodium(I)-Catalyzed [2+2+2] Cycloadditions with N-Functionalized 1-Alkynylamides: A Conceptually New Strategy for the Regiospecific Synthesis of Substituted IndolinesAngewandte Chemie International Edition in English, 1999
- N-Functionalized 1-Alkynylamides: New Building Blocks for Transition Metal Mediated Inter- and Intramolecular [2+2+1] CycloadditionsAngewandte Chemie International Edition in English, 1998
- Total Syntheses of Carazostatin, Hyellazole, and Carbazoquinocins B−FThe Journal of Organic Chemistry, 1997
- Synthesis of Carbazole AlkaloidsSynlett, 1994
- The Cobalt-Mediated [2+2+2] Cycloaddition of α,ω-Diynes to the 2,3-Double Bond of IndoleSynthesis, 1994
- [2 + 2 + 2] CycloadditionsPublished by Elsevier ,1991
- Indolo-2,3-quinodimethanes and stable cyclic analogs for regio- and stereocontrolled syntheses of [b]-annelated indolesChemical Reviews, 1989
- Cobalt-mediated [2 + 2 + 2] cycloadditions of alkynes to the indole 2,3-double bond: an extremely facile entry into the novel 4a,9a-dihydro-9H-carbazole nucleusJournal of the American Chemical Society, 1986