Abstract
An improved total synthesis of spermatinamine, an inhibitor of the anticancer target, isoprenylcysteine carboxy methyltransferase (Icmt) was accomplished from the commercially available 3,4-dibromo-4-hydroxybenzaldehyde via a high yielding reaction sequence in an overall yield of 31%.
| Original language | English |
|---|---|
| Pages (from-to) | 212-214 |
| Number of pages | 3 |
| Journal | Tetrahedron Letters |
| Volume | 52 |
| Issue number | 2 |
| DOIs | |
| State | Published - 12 Jan 2011 |
Bibliographical note
Funding Information:The research facilities and financial support by KFUPM Grant No: FT090014 are gratefully acknowledged.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Anticancer drug
- Azlactone formation
- Icmt inhibitor
- Spermatinamine
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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