Dergiler / Turkish Journal of Chemistry / 2005 / Cilt: 29 - Sayı: 5

New Alkoxyzinc Salts Mediated Chemoselective Transesterification Reactions

Sayfa
455–461
Yayın Tarihi
2005-05-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Suggested mechanisms of the transesterification reactions are discussed.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:A new chemoselective method for the transesterification of alkyl esters in the presence of in situ formed alkoxyzinc salts was developed.
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Temel Bulgular & Veri:Electron-rich esters are less reactive than electron poor ones and this is the basis for the chemoselectivity of the reaction.
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Sonuç & Katkı:Suggested mechanisms of the transesterification reactions are discussed.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Chemoselective transesterification · zinc bromide · zinc acetate

Özet

A new chemoselective method for the transesterification of alkyl esters in the presence of in situ formed alkoxyzinc salts was developed. Electron-rich esters are less reactive than electron poor ones and this is the basis for the chemoselectivity of the reaction. Suggested mechanisms of the transesterification reactions are discussed.

Abstract

A new chemoselective method for the transesterification of alkyl esters in the presence of in situ formed alkoxyzinc salts was developed. Electron-rich esters are less reactive than electron poor ones and this is the basis for the chemoselectivity of the reaction. Suggested mechanisms of the transesterification reactions are discussed.

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Bu Makaleye Atıf Yap

COŞKUN, N., ER, M. (2005). New Alkoxyzinc Salts Mediated Chemoselective Transesterification Reactions. Turkish Journal of Chemistry, Cilt: 29 - Sayı: 5, 455–461. https://ajindex.com/articles/227809

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