One pot synthesis of α-ketoamides from ethylarenes and amines: a metal free difunctionalization strategy.

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One pot synthesis of α-ketoamides from ethylarenes and amines: a metal free difunctionalization strategy.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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One pot synthesis of α-ketoami ...... difunctionalization strategy.

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One pot synthesis of α-ketoami ...... difunctionalization strategy.

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One pot synthesis of α-ketoami ...... difunctionalization strategy.

@en

One pot synthesis of α-ketoami ...... difunctionalization strategy.

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One pot synthesis of α-ketoami ...... difunctionalization strategy.

@en

One pot synthesis of α-ketoami ...... difunctionalization strategy.

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P1476

One pot synthesis of α-ketoami ...... difunctionalization strategy.

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P2093

Chun-Kai Kuo

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Mani Ramanathan

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Shiuh-Tzung Liu

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P2860

Cocrystal Structures of Primed Side-Extending α-Ketoamide Inhibitors Reveal Novel Calpain-Inhibitor Aromatic Interactions #

The introduction of P4 substituted 1-methylcyclohexyl groups into Boceprevir: a change in direction in the search for a second generation HCV NS3 protease inhibitor

Systematic comparison of peptidic proteasome inhibitors highlights the α-ketoamide electrophile as an auspicious reversible lead motif

Peptidyl alpha-ketoamides with nucleobases, methylpiperazine, and dimethylaminoalkyl substituents as calpain inhibitors

Selenium dioxide-mediated synthesis of α-ketoamides from arylglyoxals and secondary amines

Potent inhibition of enterovirus D68 and human rhinoviruses by dipeptidyl aldehydes and α-ketoamides.

Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks.

Recent Developments in General Methodologies for the Synthesis of α-Ketoamides.

Direct use of formamides as amino group sources via C-N bond cleavage: a catalytic oxidative synthesis of α-ketoamides from acetophenones and formamides under metal-free conditions.

Retinoid receptor subtype-selective modulators through synthetic modifications of RARgamma agonists.

P304

11446-11453

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P31

scholarly article

P356

10.1039/C6OB02361D

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2016-11-23T00:00:00Z

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P698

27878198

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