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Synthesis of lanopylin B1
Journal article   Peer reviewed

Synthesis of lanopylin B1

Barry B SNIDER and JINGYE JINGYE ZHOU
Journal of Organic Chemistry, Vol.70(3), pp.1087-1088
2005
PMID: 15675879

Abstract

Chemistry Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives Preparations and properties Exact sciences and technology Organic Chemistry
Phase-transfer alkylation of diethyl 2-oxopropylphosphonate (9) with 2-iodoalkyl azide afforded 40% of azido phosphonate 6, which underwent a phase-transfer Horner−Emmons Wittig reaction with heptadecanal to provide 80% of azido enone 5. An intramolecular aza-Wittig reaction with polymer-bound Ph3P in toluene at reflux completed the first synthesis of lanopylin B1 in 76% yield.

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