Simplified synthesis of peptides with non-protected amino acid hydrochlorides via four-component condensation

DOI: 10.1055/s-1992-26240

Source and publish data:

Synthesis p. 837 - 838 (1992)

Update date:2022-07-30

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Authors:

Kintscher

Martens Martens

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Article abstract of DOI:10.1055/s-1992-26240

Synthesis of sulfur containing peptide analogues, 3-(ω-aminoalkanoyl)-2,2-dimethyl-1,3-thiazolidine-4-carboxamides 2, via Ugi four-component condensation (4CC) starting from 2,5-dihydro-1,3-thiazoles 1, isocyanides and non-protected amino acid hydrochlori

Full text of DOI:10.1055/s-1992-26240

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Product name:4-Thiazolidinecarboxamide, N-cyclohexyl-3-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxopropyl]- 2,2,5,5-tetramethyl-

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