Cupric Ion Chelation Assisted Synthesis of N(α)-Protected N(ω)-Acridin-9-yl α,ω-Diamino Carboxylic Acids
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The synthesis of Nα-protected Nω-acridin-9-yl derivatives of the α,w-diamino carboxylic acids ornithine and lysine is reported. Direct introduction of the acridin-9-yl moiety to the amino side chain of the free amino acid was achieved in methanol through temporary copper(II) chelation protection of the α-amino and carboxy groups. Nα-Fmoc protection was introduced by using N-(fluoren-9-ylmethoxycarbonyloxy)succinimide in aqueous dioxan.
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2011 ◽
Vol 396-398
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pp. 1210-1212
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1962 ◽
2013 ◽
Vol 42
(1)
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pp. 96-101
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2020 ◽
Vol 23
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2020 ◽
Vol 22
(9)
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pp. 657-662
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1971 ◽
Vol 11
(1)
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pp. 112-114
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