Cyanation of nucleophilic alkynes: easy approach to element-substituted α-cyanoenamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Synthesis of α‐Cyanoenamines by Cyanation of α‐Bromoimmonium Bromides and Dehydrobromination of β‐bromo‐α‐(dialkylamino)nitriles
2. The addition of phosphorus halides to ynamines. Ring-chain tautomerism of phosphirene with isomeric open structure
3. Catalyzed and non-catalyzed addition reactions to the triple bond
4. The stereochemistry of organometallic compounds. XXIV. Nickel(0)-catalysed additions of hydrogen cyanide to alkynes
5. The Stereochemistry of Organometallic Compounds. XXXII. Hydrocyanation of Derivatives of Amino Alkynes
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2. Nickel-catalysed regio- and stereoselective hydrocyanation of alkynoates and its mechanistic insights proposed by DFT calculations;Organic & Biomolecular Chemistry;2024
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4. Zinc‐Catalyzed Hydrocyanation of Ynamides and Photoisomerization, a General and Selective Access to E and Z Trisubstituted α‐Enamidonitriles;Chemistry – A European Journal;2023-04-19
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