Reactions of Alkyl Azides and Ketones as Mediated by Lewis Acids: Schmidt and Mannich Reactions Using Azide Precursors
- 15 July 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (30), 7226-7232
- https://doi.org/10.1021/ja000490v
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Aliphatic azides as lewis bases. Application to the synthesis of heterocyclic compoundsJournal of Heterocyclic Chemistry, 1996
- One-Step Conversion of Aldehydes to Oxazolines and 5,6-Dihydro-4H-1,3-oxazines Using 1,2- and 1,3-Azido AlcoholsThe Journal of Organic Chemistry, 1996
- Synthesis of Functionalized N-Alkyl Heterocycles from Ketones by a Sequential Ring Expansion/Nucleophilic Addition ProcessThe Journal of Organic Chemistry, 1996
- Intramolecular Schmidt Reactions of Alkyl Azides with Ketones: Scope and Stereochemical StudiesJournal of the American Chemical Society, 1995
- Efficient Nitrogen Ring-Expansion Process Facilitated by in Situ Hemiketal Formation. An Asymmetric Schmidt ReactionJournal of the American Chemical Society, 1995
- Generation of a Lewis acid activated formaldimine and its reaction with enol silyl ethers. N-Unsubstituted aminomethylationThe Journal of Organic Chemistry, 1992
- A highly convergent asymmetric synthesis of the C(19)-C(27) segment of rifamycin S: an application of enantiodifferentiating acetalization with menthoneThe Journal of Organic Chemistry, 1992
- Electrocatalytic four-electron reduction of dioxygen by iridium porphyrins adsorbed on graphiteJournal of the American Chemical Society, 1986
- The Preparation and Structural Proof of Thiophene Amidone and IsoamidoneJournal of the American Chemical Society, 1955
- Ketoxime-O-sulfonic Acids1Journal of the American Chemical Society, 1948