Journal
ORGANIC LETTERS
Volume 9, Issue 6, Pages 969-971Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol062960h
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The first, enantiocontrolled total synthesis of (+)-sundiversifolide has been accomplished using the sequential ring-closing metathesis, [3,3]sigmatropic rearrangement, and iodolactonization for the key assembly of the cis-fused oxabicyclo[5.3.0] decene framework of the natural product.
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