A highly diastereoselective series of Nicholas cyclisation reactions of N-Boc-protected propargylamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference24 articles.
1. The synthesis and biological evaluation of a range of novel functionalised benzopyrans as potential potassium channel activators
2. Chemistry and synthetic utility of cobalt-complexed propargyl cations
3. Novel tandem diastereoselective cyclisation reactions of dicobalt hexacarbonyl complexed propargyl cations
4. A diastereoselective synthesis of benzopyrans using a novel intramolecular Nicholas reaction in the key cyclisation step
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1. Propargylic Coupling Reactions via Bimetallic Alkyne Complexes: The Nicholas Reaction;Organic Reactions;2020-07-24
2. Relative Reactivity of Benzothiophene-Fused Enediynes in the Bergman Cyclization;The Journal of Organic Chemistry;2018-02-16
3. Cobalt-Catalysed Bond Formation Reactions; Part 2;Synthesis;2015-12-03
4. A Tin(IV) Chloride Promoted Tandem C–O Bond Cleavage/Nazarov Cyclization/Nucleophilic Addition Reaction of 1,1-Disubstituted Allylic Ethers toward the Synthesis of Multisubstituted Indenes;Organic Letters;2015-10-14
5. Octacarbonyldicobalt;Encyclopedia of Reagents for Organic Synthesis;2014-05-27
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