Synthesis of Trialkylhydroxylamines by Stepwise Reduction of O-Acyl N,N-Disubstituted Hydroxylamines: Substituent Effects on the Reduction of O-(1-Acyloxyalkyl)hydroxylamines and on the Conformational Dynamics of N-Alkoxypiperidines
Author:
Affiliation:
1. Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00717
Reference48 articles.
1. Asymmetric Synthesis of Polyhydroxylated N-Alkoxypiperidines by Ring-Closing Double Reductive Amination: Facile Preparation of Isofagomine and Analogues
2. NO Bond as a Glycosidic-Bond Surrogate: Synthetic Studies Toward PolyhydroxylatedN-Alkoxypiperidines
3. Synthesis and Evaluation of Di- and Trimeric Hydroxylamine-Based β-(1→3)-Glucan Mimetics
4. Synthesis of N,N,O-Trisubstituted Hydroxylamines by Stepwise Reduction and Substitution of O-Acyl N,N-Disubstituted Hydroxylamines
5. Improved Procedure for the Reductive Acetylation of Acyclic Esters and a New Synthesis of Ethers
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