Solid‐Phase Synthesis of Glycopeptide Amides under Mild Conditions: Morphiceptin Analogues

Eduard Bardají; Josep L. Torres; Pere Clapés; Fernando Albericio; George Barany; Gregorio Valencia

doi:10.1002/anie.199002911

Solid‐Phase Synthesis of Glycopeptide Amides under Mild Conditions: Morphiceptin Analogues

Eduard Bardají, Josep L. Torres, Pere Clapés, Fernando Albericio, George Barany, Gregorio Valencia

Chemistry (Twin Cities)

Research output: Contribution to journal › Article › peer-review

25 Scopus citations

Abstract

Membrane glycoproteins belong to the most important compounds in living nature. The glycoprotein amides (morphiceptin analogous) have now become readily accessible by a solid‐phase method (glycosyl is galacto‐ or glucopyranosyl). Upon detachment from the carrier, the sensitive glycosidic bond remains intact. (Figure Presented.)

Original language	English (US)
Pages (from-to)	291-292
Number of pages	2
Journal	Angewandte Chemie International Edition in English
Volume	29
Issue number	3
DOIs	https://doi.org/10.1002/anie.199002911
State	Published - Mar 1990

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title = "Solid‐Phase Synthesis of Glycopeptide Amides under Mild Conditions: Morphiceptin Analogues",

abstract = "Membrane glycoproteins belong to the most important compounds in living nature. The glycoprotein amides (morphiceptin analogous) have now become readily accessible by a solid‐phase method (glycosyl is galacto‐ or glucopyranosyl). Upon detachment from the carrier, the sensitive glycosidic bond remains intact. (Figure Presented.)",

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AU - Albericio, Fernando

AU - Barany, George

AU - Valencia, Gregorio

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AB - Membrane glycoproteins belong to the most important compounds in living nature. The glycoprotein amides (morphiceptin analogous) have now become readily accessible by a solid‐phase method (glycosyl is galacto‐ or glucopyranosyl). Upon detachment from the carrier, the sensitive glycosidic bond remains intact. (Figure Presented.)

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Solid‐Phase Synthesis of Glycopeptide Amides under Mild Conditions: Morphiceptin Analogues

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