New synthesis of macrocyclic crown-formazans from pyruvic acid derivatives
β Scribed by Yehia A. Ibrahim; Ahmed H.M. Elwahy; Ashraf A. Abbas
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 704 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
β¦ Synopsis
Absfmk
The macmcyclic crown-formamas 7ac. 121-g were prepared by the azc coupling of the appropriate bisdiazoaium salts 4a-c with pyruvic acid and a&ruvic acids 8~. The ready accessability of the latters e&m an easy access towards l,$-symnWically disubstihW4i-3-arylformazam e.g. 1Oa-g as well as their macmcyclic crown derivatives of expected valuable applications.
π SIMILAR VOLUMES
## A-c lbouew ~les(land2)incorporatingaCrOWnethQandaglucosclnithave beensyn~efficientiyinsix~froma-allylgl ~de.Pdiiinary complexatim Studic3wilhakalimctalmdmmtoniumiatsaredcscribcd.
The synthesis of new 16-, 18-, 19-or 20-membered secondary tetralactams with L-tartaric acid or 13-hydroxyglutaric acid moieties is investigated. The stepwise synthesis with an intermediate diamide diamine provides overall good yields (30-55%) compared with other processes using an intermediate diam