## Abstract Symmetrically substituted 1,3‐diynes containing hydroxyalkyl (1a‐d), bromoalkyl (1e‐h) (diphenylphosphinyl) (1i‐k) and carboxyalkyl (2a‐d) substituents have been prepared and characterised; the phosphine derivative (1k) has been converted with alkyl iodides (RI; R = Me, Et) into bis(pho
Mg-Al 3:1 hydrotalcite catalyst in the synthesis of cyclopropane carboxylic acid derivatives
✍ Scribed by Zoltán Finta; Zoltán Hell; Daniella Balán; Agnieszka Cwik; Sándor Kemény; François Figueras
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 134 KB
- Volume
- 161
- Category
- Article
- ISSN
- 1381-1169
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✦ Synopsis
The non-activated Mg-Al 3:1 hydrotalcite is a suitable basic catalyst both in the intramolecular cyclization reaction of malonic acid allylic esters into bicyclic cyclopropane carboxylic acid lactones and the intermolecular cyclization reaction of dibromoethane and diethyl malonate into cyclopropane dicarboxylic acid diester. The optimal reaction conditions of the intramolecular cyclization were determined using a 2 4 factorial design. An interesting effect on the diastereoselectivity of the intramolecular cyclization was observed compared with the diastereoselectivity of this cyclization using solid potassium carbonate as base.
📜 SIMILAR VOLUMES
## Abstract magnified image In this study, the synthesis of series of 2‐benzo[__b__]furan‐substituted 1,3,4‐oxadiazole derivatives using readily available 2‐benzo[__b__]furan carboxylic acid hydrazide as starting material has been investigated. J. Heterocyclic Chem., (2009).
Mg/Al hydrotalcite, a heterogeneous base catalyst, was found to be highly effective for the synthesis of 2aminochromenes via a multicomponent reaction of aromatic aldehydes, malononitriles and 1-naphthol under microwaves. The reaction is rapid, clean and gives the products in high yields. The cataly