An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

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An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

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2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年學術文章

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An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

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An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

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An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

@en

An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

@nl

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An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

@en

An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

@nl

P1476

An efficient synthesis of the 4'-epimer of 2-fluoronoraristeromycin.

@en

P2093

Junyan Zhong

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Quachel Bazile

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Tesfaye Serbessa

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P2860

Highly efficient stereoconservative amidation and deamidation of alpha-amino acids

Inhibition of human immunodeficiency virus type 1 replication by blocking IkappaB kinase with noraristeromycin.

Plasmodium falciparum S-adenosylhomocysteine hydrolase. cDNA identification, predicted protein sequence, and expression in Escherichia coli.

John Montgomery's legacy: carbocyclic adenosine analogues as SAH hydrolase inhibitors with broad-spectrum antiviral activity.

Synthesis of 2-fluoronoraristeromycin and its inhibitory activity against Plasmodium falciparum S-adenosyl-L-homocysteine hydrolase.

Crystal structure of S-adenosyl-L-homocysteine hydrolase from the human malaria parasite Plasmodium falciparum.

Mutational analyses of Plasmodium falciparum and human S-adenosylhomocysteine hydrolases.

Synthesis of 4'-modified noraristeromycins to clarify the effect of the 4'-hydroxyl groups for inhibitory activity against S-adenosyl-L-homocysteine hydrolase.

P304

1435-1437

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P31

scholarly article

P356

10.1016/J.TETLET.2012.01.047

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P433

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P478

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P577

2012-01-20T00:00:00Z

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P5875

225293823

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P698

22690021

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P932

3370682

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