Preparation of C-alkylated macrocyclic polyamines
β Scribed by Iwao Tabushi; Yoichi Taniguchi; Hidefumi Kato
- Book ID
- 104243940
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 170 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Macrocyclic polyamines have attracted increasing attention because of their unique property to form very stable chelates with various heavy metal ions l-6) .
π SIMILAR VOLUMES
Β±)-Azemacrolides were synthesized via lipase-catslyzed intmmolccular cyclization of (~-)-hydroxy-azaesters. Further, the size of the macrocyclic lactones formed could be altered by the substituent on the nitrogen atom. This allows one to prepare a combinatorial library of azamacrolides from a small
multi-membered O,N,S-heterocycles multi-membered O,N,S-heterocycles (with at least 2 different heteroatoms