Regioselective 1,2-additions of alcohols to allenamides mediated by N-Iodosuccinimide: Synthesis of N,O-aminals-Reference-Cited by-同舟云学术

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Regioselective 1,2-additions of alcohols to allenamides mediated by N-Iodosuccinimide: Synthesis of N,O-aminals

Published:2018-09 Issue:39 Volume:74 Page:5674-5682
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Yuan Xiao,Re He Man Xi Jia Ai Ti,Li Xiao-Xiao,Zhao Zhi-Gang

Funder

Project of Science and Technology Department of Sichuan Province

Fundamental Research Funds of Central Universities

Southwest Minzu University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. Chemistry of Ketene N,S-Acetals: An Overview

2. Organocatalytic Asymmetric Direct Alkylation of α-Diazoester via C−H Bond Cleavage

3. Advanced Organic Chemistry Reactions, Mechanisms and Structure;March,1985

4. Discovery of MK-8742: An HCV NS5A Inhibitor with Broad Genotype Activity

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3. Regio- and Stereoselective Hexafluoroisopropoxylation and Trifluoroethoxylation of Allenamides;The Journal of Organic Chemistry;2024-01-02

4. Regiocontrollable Difunctionalization of N-Allenamines;Chinese Journal of Organic Chemistry;2024

5. NIS-mediated regioselective addition of allenamides with pyrazoles: synthesis of iodo-substituted allylic pyrazoles;New Journal of Chemistry;2023

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