4.7 Article

Total synthesis and absolute stereochemistry of pentenocin B, a novel interleukin-1β converting enzyme inhibitor

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 69, Issue 5, Pages 1744-1747

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo035430x

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Four possible diastereomers of pentenocin B were synthesized in a stereocontrolled manner, and the first total synthesis of a natural enantiomer of (+)-pentenocin B unequivocally established the absolute stereochemistry to be 4S,5R,6R.

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