Synthesis of (+)-Tetrahydropseudodistomin

DOI: 10.1021/jo00062a003

Source and publish data:

Journal of Organic Chemistry p. 2650 - 2651 (1993)

Update date:2022-09-26

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Authors:

Knapp, Spencer

Hale, Jeffrey J.

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Article abstract of DOI:10.1021/jo00062a003

The stereocontrolled synthesis of (+)-tetrahydropseudodistomin (3) from D-serine features the use of the dibenzyltriazone group for amino protection and establishes the absolute stereochemistry of the naturally occuring calmodulin antagonists pseudodistomin A and B (1 and 2b, respectively).

Full text of DOI:10.1021/jo00062a003

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