98806-92-9Relevant academic research and scientific papers
Synthesis of Proline Derivatives by 1,3-Dipolar Cycloaddition of Azomethine Ylide Generated from an Organosilicon Compound
Imai, Nobuyuki,Terao, Yoshiyasu,Achiwa, Kazuo
, p. 2085 - 2089 (2007/10/02)
The 1,3-dipolar cycloaddition of azomethine ylides generated from methyl N-(trimethylsilylmethyl)iminoacetate and benzyl bromide or a catalytic amount of trifluoroacetic acid has been found to give the corresponding proline derivatives.
A NEW SYNTHETIC METHOD FOR PROLINE DERIVATIVES VIA THE AZOMETHINE YLIDE INTERMEDIATE GENERATED FROM METHYL N-(TRIMETHYLSILYLMETHYL)IMINOACETATE
Imai, Nobuyuki,Terao, Yoshiyasu,Achiwa, Kazuo
, p. 1107 - 1110 (2007/10/02)
Proline derivatives were found to be synthesized by the 1,3-dipolar cycloaddition of the azomethine ylide, produced from methyl N-(trimethylsilylmethyl)iminoacetate and benzyl bromide or a catalytic amount of trifluoroacetic acid, to conjugated olefins.
