Lithium (trimethylsilyl)acetylide can be used as a reagent:
In the transmetalation and nucleophilic displacement reactions.[1]
To prepare propargylic alcohol derivatives by reacting with aldehydes and ketones.[1]
To synthesize α,βynones by treating with Weinreb amide or with isoxazolidide.[1]
Along with Grignard reagent to convert γ- and δ-thiolactams to thioiminium salts, which are employed as key intermediates to produce disubstituted pyrrolidines.[2]
Reacts with halotriazines to produce conductive, anisotropic carbon-nitrogen materials.[3]
Packaging
The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Sequential addition reaction of lithium acetylides and Grignard reagents to thioiminium salts from thiolactams leading to 2, 2-disubstituted cyclic amines
M Toshiaki, et al.
Tetrahedron, 62(26), 6312-6320 (2006)
Chemistry of Materials, 6, 636-636 (1994)
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