New Approach for the General Synthesis of Oxotetrahydroindoles via Intramolecular Cycloadditions of Azomethine Ylides with Tethered Alkynes
- 1 February 1997
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 62 (4) , 982-991
- https://doi.org/10.1021/jo9614598
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Synthesis of FPL 64176 by 1,3-Dipolar CycloadditionThe Journal of Organic Chemistry, 1995
- Azasulfonamidopeptides as peptide bond hydrolysis transition state analogues. Part 1. Synthetic approachesJournal of the Chemical Society, Perkin Transactions 1, 1994
- 2-Chloro-4,6-dimethoxy-1,3,5-triazine. A New Coupling Reagent for Peptide SynthesisSynthesis, 1987
- Intramolecular munchnone cycloadditions: preparation and chemistry of the intramolecular dipolar cycloadductsThe Journal of Organic Chemistry, 1985
- An intramolecular Diels–Alder strategy to forskolinJournal of the Chemical Society, Chemical Communications, 1985
- Total synthesis of a mitoseneThe Journal of Organic Chemistry, 1984
- Reaction of 2-aminobenzazoles with dimethyl 2-aminofumarate. Synthesis and nuclear magnetic resonance spectroscopy of 4-oxopyrimido[2,1-b]benzazolesThe Journal of Organic Chemistry, 1979
- Comments on the putative stereoselectivity in cysteine-aldehyde reactions. Selective C(2) inversion and C(4) epimerization in thiazolidine-4-carboxylic acidsJournal of the American Chemical Society, 1979
- The Mitomycin Antibiotics. Synthetic Studies. IX.1 A Versatile New Method of Indole SynthesisJournal of the American Chemical Society, 1965
- Azlactones as 1,3-Dipoles; A New Pyrrole SynthesisAngewandte Chemie International Edition in English, 1964