4.8 Article

A formal total synthesis of (+)-zincophorin. Observation of an unusual urea-directed Stork-Crabtree hydrogenation

Journal

ORGANIC LETTERS
Volume 9, Issue 11, Pages 2199-2202

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol070791a

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Funding

  1. NIGMS NIH HHS [GM066055] Funding Source: Medline

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A formal total synthesis of (+)-zincophorin via interception of Miyashita's advanced intermediates is described here. This effort features the first synthetic application of an inverse demand hetero [4 + 2] cycloaddition of a chiral allenamide, and the observation of an unusual urea directed Stork-Crabtree hydrogenation.

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