256382-52-2

Upstream product

• 40217-17-2 (R)-4-(phenylmethyl)-2-oxazolidinone 
• 106-96-7 propargyl bromide 
• 256382-76-0 (R)-4-Benzyl-3-prop-2-ynyl-oxazolidin-2-one 

Downstream Products

• 1150519-11-1 C₁₈H₂₁NO₂ 
• 1150519-09-7 C₁₆H₁₇NO₂ 
• 1150518-38-9 C₂₀H₁₉NO₂ 
• 1150518-36-7 C₁₇H₂₁NO₂ 
• 1188475-14-0 C₁₅H₁₇NO₂ 
• 1188475-13-9 C₁₅H₁₇NO₂ 
• 1215847-87-2 C₃₃H₃₇NO₃Si 
• 1215847-91-8 C₂₀H₂₃NO₃ 
• 1215847-86-1 C₃₃H₃₇NO₃Si 
• 1215847-89-4 C₂₀H₂₃NO₃ 
• 1215847-92-9 C₂₇H₃₀N₂O₄S 

Relevant academic research and scientific papers

A simple one-pot preparation of N-allenyl amides, ureas, carbamates and sulfonamides using a DMSO/tBuOK protocol

A one-pot transformation of amides, ureas, carbamates and sulfonamides into synthetically useful N-allenyl analogues using a tBuOK/DMSO protocol is reported. The procedure is experimentally simple and robust, and provides N-allenyl analogues, c

Efficient preparations of novel ynamides and allenamides

Practical syntheses of a series of novel ynamides and allenamides are described here. While a base-induced isomerization protocol of propargyl amides leads to an array of chiral and achiral allenamides, ynamides are prepared from enamides via bromination followed by base-induced elimination of the Z-bromoenamides. These ynamides and allenamides possess improved thermal stability compared to ynamines and allenamines. They can be isolated, purified, and handled with ease, and thus, should be synthetically more useful than traditional ynamines and allenamines.

First stereoselective inverse demand [4 + 2] cycloaddition reactions of novel chiral allenamides with heterodienes. Preparation of highly functionalized 2-arylpyranyl heterocycles

matrix presented The first stereoselective inverse demand [4 + 2] cycloaddition reactions of chiral allenamides with heterodienes are described here. These reactions lead to stereoselective synthesis of highly functionalized pyranyl heterocycles. A mechan