Selective cleavage of the N-propargyl group from sulfonamides and amides under ruthenium catalysis-Reference-Cited by-同舟云学术

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Selective cleavage of the N-propargyl group from sulfonamides and amides under ruthenium catalysis

Published:2018-05 Issue:20 Volume:59 Page:1902-1905
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wang Jingjing,Li Feng,Pei Wenlong,Yang Mixue,Wu Yidan,Ma Danyang,Zhang Furong,Wang Jianhui

Funder

National Natural Science Foundation of China

Key Science Research of Education Committee in Henan Province

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference37 articles.

1. The evolving role of natural products in drug discovery

2. Heterocyclic Chemistry in Drug Discovery;Li,2013

3. AXL Inhibitors in Cancer: A Medicinal Chemistry Perspective

4. Targeting Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 (MAPKAPK2, MK2): Medicinal Chemistry Efforts To Lead Small Molecule Inhibitors to Clinical Trials

5. Protective Groups in Organic Synthesis;Greene,2007

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2. Hydrazine-assisted one-pot depropargylation and reduction of functionalized nitro calix[4]arenes;Russian Chemical Bulletin;2023-04

3. Visible‐light Induced Cerium‐catalyzed N‐Demethylation of N‐Methyl Amides under Air Conditions;Advanced Synthesis & Catalysis;2023-01-24

4. Photomediated Spirocyclization of N-Benzyl Propiolamide with N-Iodosuccinimide for Access to Azaspiro[4.5]deca-6,9-diene-3,8-dione;J ORG CHEM;2022

5. Photomediated Spirocyclization of N-Benzyl Propiolamide with N-Iodosuccinimide for Access to Azaspiro[4.5]deca-6,9-diene-3,8-dione;The Journal of Organic Chemistry;2022-06-09

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