Synthetic studies towards the synthesis of western and eastern chloropeptin I, II subunits

DOI: 10.3987/COM-99-8514

Source and publish data:

Heterocycles p. 2041 - 2063 (1999)

Update date:2022-08-04

Topics:

Authors:

Roussi, Georges

Gonzalez Zamora, Eduardo

Carbonnelle, Annie-Claude

Beugelmans, Rene

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Article abstract of DOI:10.3987/COM-99-8514

The western subunit (16-membered ring) was synthesized by the intramolecular SNAr reaction while the first 16-membered ring compound was obtained as a model of the eastern subunit via an intramolecular Ni⁰ mediated coupling reaction.

Full text of DOI:10.3987/COM-99-8514

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Product name:[(R)-(3,5-dichloro-4-methoxyphenyl)-(S)-(2-hydroxy-1-phenylethylamino)]acetic acid methyl ester

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