A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes-Reference-Cited by-同舟云学术

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A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes

Published:2014-12 Issue:52 Volume:55 Page:7186-7189
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yan Zhaohua,Xu Yun,Tian Weisheng

Funder

National Natural Science Foundation of China

Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. Structures of TMC-95A−D: Novel Proteasome Inhibitors from Apiospora montagnei Sacc. TC 1093

2. The Crocacins, Novel Antifungal and Cytotoxic Antibiotics fromChondromyces crocatus andChondromyces pediculatus (Myxobacteria): Isolation and Structure Elucidation

3. Chondriamides A and B, new indolic metabolites from the red alga Chondria sp.

4. Salicylihalamides A and B, Novel Cytotoxic Macrolides from the Marine Sponge Haliclona sp.

5. Cinnamamide derivatives from Clausena lansium

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1. Approach to α-fluorinatedacetoxy ketones by fluoroacetoxylation of alkynes with hyper-valent iodine(III) reagents;Tetrahedron Letters;2023-11

2. Beckmann rearrangement catalysis: a review of recent advances;New Journal of Chemistry;2020

3. Synthesis, characterization, DFT and molecular docking studies for novel 1,5-diphenylpenta-1,4-dien-3-one O-benzyl oximes;Journal of the Iranian Chemical Society;2019-05-24

4. Tertiary Enamides: Versatile and Available Substrates in Synthetic Chemistry;Current Organic Synthesis;2019-02-04

5. Recent Progress in Beckmann Rearrangement;Chinese Journal of Organic Chemistry;2019

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