Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

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Cysteine Isocyanide in Multicomponent Reaction: Synthesis of Peptido-Mimetic 1,3-Azoles.Concise Synthesis of Tetrazole Macrocycle Synthetic fermentation of β-peptide macrocycles by thiadiazole-forming ring-closing reactions.

P2860

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P2860

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

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http://www.wikidata.org/entity/Q41092301

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

@en

type

Item

label

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

@en

prefLabel

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

@en

P1476

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics

@en

P2093

Enrico Bergamaschi

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

Thimmalapura M Vishwanatha

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

P2860

Incorporation of Non-natural Amino Acids Improves Cell Permeability and Potency of Specific Inhibitors of Proteasome Trypsin-like Sites

Dithiol amino acids can structurally shape and enhance the ligand-binding properties of polypeptides

Synthesis of proteins by native chemical ligation

Solution- and Solid-Phase Macrocyclization of Peptides by the Ugi-Smiles Multicomponent Reaction: Synthesis of N-Aryl-Bridged Cyclic Lipopeptides.

Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity.

Synthesis of a novel macrocyclic library: discovery of an IGF-1R inhibitor.

Stereochemical control of skeletal diversity.

Recent developments in isocyanide based multicomponent reactions in applied chemistry.

Designing peptide receptor agonists and antagonists.

Glutathione conjugates and their synthetic derivatives as inhibitors of glutathione-dependent enzymes involved in cancer and drug resistance.

P304

3195-3198

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P31

scholarly article

P356

10.1021/ACS.ORGLETT.7B01324

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

P407

English

P433

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

P478

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

P50

A Dömling

P577

2017-06-05T00:00:00Z

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

P698

28581763

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P932

5477004

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

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

about

P2860

P2860

Sulfur-Switch Ugi Reaction for Macrocyclic Disulfide-Bridged Peptidomimetics.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932