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Can I read Synthesis of Symmetrically and Unsymmetrically Substituted .alpha.-Diones from Organometallic Reagents and 1,4-Dialkylpiperazine-2,3-diones on EtoBox?

Synthesis of Symmetrically and Unsymmetrically Substituted .alpha.-Diones from Organometallic Reagents and 1,4-Dialkylpiperazine-2,3-diones by Ulrich T. Mueller-Westerhoff; Ming Zhou is a Chemistry article available to read on EtoBox.

What is Synthesis of Symmetrically and Unsymmetrically Substituted .alpha.-Diones from Organometallic Reagents and 1,4-Dialkylpiperazine-2,3-diones about?

The reaction of an equimolar mixture ofN,"-dialkylethylenediamines and diethyl oxalate in diethyl ether or 2-propanol leads to 1,4-dialkylpiperazine-2,3-diones. As cyclic and nearly planar tetraalkyl oxamides, these compounds are able to react with 2 equiv of organolithium or Grignard compounds to form, after hydrolysis, symmetrically substituted a-diones in excellent yields. The sequential addition of 1 equiv each of two different organolithium compounds affords unsymmetrically substituted a-diones when the more soluble longer chain dialkyl derivatives of piperazine-2,3-dione are employed. The dialkylethylenediamines can conveniently be recovered and recycled to the 1,4dialkylpiperazine-2,3-diones in good yields.

Who reads Synthesis of Symmetrically and Unsymmetrically Substituted .alpha.-Diones from Organometallic Reagents and 1,4-Dialkylpiperazine-2,3-diones?

It is typically read by researchers, students, and practitioners in Chemistry.

Author
Ulrich T. Mueller-Westerhoff; Ming Zhou
Publisher
American Chemical Society (ACS)
Published
1994
Language
EN
Field
Chemistry (Physical Sciences)

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