Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 73, Issue 21, Pages 8452-8457Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo801666t
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Funding
- NIH [GM069352, CA 108488, T32 GM008505, 1 S 10 RR0 8389-01]
- NSF [CHE-9208463]
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The synthesis of didemniserinolipid B utilizing a ketalization/ring-closing metathesis (K/RCM) strategy is described. In the course of this work, a novel 2-allyl-4-fluorophenyl auxiliary for relay ring-closing metathesis (RRCM) was developed, which increased the yield of the RCM. The resulting 6,8-dioxabicyclo[3.2.1]octene core was selectively functionalized by complimentary dihydroxylation and epoxidation routes to install the C10 axial alcohol. This bicyclic ketal core was further functionalized by etherification and an alkene cross metathesis with an unsaturated a-phenylselenyl ester en route to completing the total synthesis.
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