An Efficient Synthesis of Selectively Functionalized Spermidine
- 1 January 1994
- journal article
- research article
- Published by Georg Thieme Verlag KG in Synthesis
- Vol. 1994 (01) , 37-39
- https://doi.org/10.1055/s-1994-25400
Abstract
A method is described for the synthesis of selectively protected Boc, Fmoc or Z-spermidine derivatives. The starting spermidine, N8-benzyloxycarbonyl-N 1-tert-butoxycarbonylspermidine is prepared using a reductive amination.Keywords
This publication has 0 references indexed in Scilit: