Tin-Indium Mediated and Microwave Assisted Propargylation of Aldehydes with Propargyl Bromide
Author:
Publisher
Wiley
Subject
General Chemistry
Reference45 articles.
1. Diastereoselective Propargylation of .alpha.-Alkoxy Aldehydes with Propargyl Bromide and Zinc. A Versatile and Efficient Method for the Synthesis of Chiral Oxygenated Acyclic Natural Products
2. Asymmetric Synthesis of anti-Homopropargylic Alcohols from Aldehydes and Chiral Sulfonimidoyl Substituted Bis(allyl)titanium Complexes through Generation and Elimination of Novel Chiral Alkylidenecarbene (Dimethylamino)sulfoxonium Ylides
3. Regio- and Diastereoselective Allenylation of Aldehydes in Aqueous Media: Total Synthesis of (+)-Goniofufurone1
4. Synthesis of Nonracemic β-Hydroxy Ketones and Carbonate Derivatives from Homopropargylic Alcohols through Iodolactonization
5. Addition of Allenylzinc Reagents, Prepared in Situ from Nonracemic Propargylic Mesylates, to Aldehydes. A New Synthesis of Highly Enantioenriched Homopropargylic Alcohols
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2. Making and breaking of Zn–C bonds in the cases of allyl and propargyl organozincs;Tetrahedron;2021-06
3. One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions;Letters in Organic Chemistry;2020-05-20
4. Synthesis, characterization of active Sn(0), and its application in selective propargylation of aldehyde at room temperature in water;Canadian Journal of Chemistry;2019-01
5. Propargylation of Aldehydes Using Potassium Allenyltrifluoroborate;Synthesis;2014-09-25
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