A two step synthesis of a key unit B precursor of cryptophycins by asymmetric hydrogenation

A novel highly enantioselective two step access to a unit B precursor of cryptophycins in good yields from commercially available starting materials has been developed. The key step is an asymmetric hydrogenation using the commercially available [(COD)Rh-( R , R )-Et-DuPhos]BF 4 catalyst. The synthe...

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Bibliographic Details
Published inBeilstein journal of organic chemistry Vol. 7; no. 1; pp. 243 - 245
Main Authors Sammet, Benedikt, Brax, Mathilde, Sewald, Norbert
Format Journal Article
LanguageEnglish
Published Germany Beilstein-Institut 22.02.2011
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