Annabella Vitalone, Janice McColl, Dean Thome, Lucio G Costa, Beatrice Tita
Index: J. Comb. Chem. 8(3) , 435-9, (2006)
Full Text: HTML
We describe parallel/combinatorial, solid-phase, supported synthesis of diverse hydroxamates using a common intermediate, an N-derivatized, O-linked hydroxylamine. The method allows the concurrent synthesis of both N-alkyl and N-H hydroxamates and is compatible with a wide range of chemical transformations. The synthesis of NH hydroxamates includes protection of the nitrogen with a 2,4-dimethoxybenzyl group at the stage of polymer-supported benzyloxyamine. The protecting group eliminates side reactions caused by the presence of a free hydroxamate NH group and is simultaneously removed during cleavage of target compounds from the solid support. The chemical route has been thoroughly tested on model compounds with several linkers, and a high yield and purity synthesis of more than 50 hydroxamates, designed to inhibit cell proliferation of breast cancer cell lines, is described.
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
2,4-Dimethoxybenzylamine
CAS:20781-20-8 |
C9H13NO2 |
Total synthesis of (-)-muraymycin D2 and its epimer.
2010-03-05 [J. Org. Chem. 75(5) , 1366-77, (2010)] |
Application of the Ugi reaction for the one-pot synthesis of...
2009-07-03 [J. Org. Chem. 74(13) , 4870-3, (2009)] |
Synthesis of N-hydroxythiourea.
1976-02-01 [J. Med. Chem. 19(2) , 336-7, (1976)] |
CCR5 antagonists as anti-HIV-1 agents. 1. Synthesis and biol...
2004-01-01 [Chem. Pharm. Bull. 52 , 63-73, (2004)] |
Synthesis of 5-substituted 4-O-methyl tetramates. Jones RC a...
[Tetrahedron Lett. 27(43) , 5285-5288, (1986)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved