Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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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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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement.

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P1476

Synthesis of gem-diamino acid derivatives by a Hofmann rearrangement

@en

P2093

Emanuele Aresu

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Federico Ramadori

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Simona Gasbarri

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P2860

Peptides and proteins as a continuing exciting source of inspiration for peptidomimetics.

The partial retro-inverso modification: a road traveled together.

Short malonyl dehydro peptides as potential scaffolds for peptidomimetics by an efficient Knoevenagel reaction.

Synthesis, structure and conformation of partially-modified retro- and retro-inverso psi[NHCH(CF3)]Gly peptides.

Facile incorporation of urea pseudopeptides into protease substrate analogue inhibitors.

Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement.

Screening of electrophilic compounds yields an aziridinyl peptide as new active-site directed SARS-CoV main protease inhibitor.

Brønsted acid-catalyzed imine amidation.

Peptides containing acylated C-terminal gem diamines: novel irreversible inactivators of the cysteine and serine proteinases.

On the mechanism of decomposition of geminal diamines

P2888

s00726-012-1428-2

P304

977-982

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P31

scholarly article

P356

10.1007/S00726-012-1428-2

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P433

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

P478

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P50

Lucio Pellacani

Stefania Fioravanti

P577

2012-11-22T00:00:00Z

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P698

23179086

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