Knoevenagel Condensation of α-Chloralose Derivative

Gökhan KÖK

doi:10.3390/ecsoc-11-01304

Previous Article in event

An Easy Synthesis of 5-Nitro-Thiophenes and 3-Amino-2-Nitro-Thiophenes

Next Article in event

A Versatile Method for the Elaboration of Diversely Substituted N-Alkylated and Free-NH Isoindolinones. Application to the Asymmetric Synthesis of the C3-Substituted Models

Knoevenagel Condensation of α-Chloralose Derivative

Gökhan KÖK

¹ Celal Bayar University, Faculty of Art and Sciences, Chemistry Department, Manisa 45030, Turkey

Published: 30 November 2007 by MDPI in The 11th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis

https://doi.org/10.3390/ecsoc-11-01304

Abstract: α-chloralose derivative aldehyde reacted with malonic acid via Knoevenagel condensation. The structure of α,β-unsaturated carboxylic acid product was characterized with spectroscopic methods.

Keywords: Knoevenagel condensation; Unsaturated sugar; chloralose.

View paper

DOI
See at publisher website
Bookmark
Cite
Additional options

37 Reads
0 Recommendations

Gökhan KÖK