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A Stille cyclisation approach to (−)-periplanone-B: studies in alkene-selective ring-closing metathesis and an improved chromium(II)-mediated synthesis of (E )-alkenylstannanes from aldehydes
35
Citations
46
References
1999
Year
Cross-coupling ReactionDerivativesHeterocyclicAlkene-selective Ring-closing MetathesisDienone 7Natural SciencesAlkene MetathesisDiversity-oriented SynthesisOrganic ChemistryImproved ChromiumChemistry-Dienone 25PharmacologyStille Cyclisation Approach
A synthesis of the dienone 7 via an efficient intramolecular Stille cross-coupling reaction, an improved chromium(II)-mediated synthesis of (E)-alkenylstannanes from aldehydes using Bu3SnCHI2 in DMF, and a synthesis of the substituted (–)-dienone 25 via ring-closing alkene metathesis to give dihydropyran 22 are described. The synthesis of (–)-dienone 25 constitutes a formal synthesis of (–)-periplanone-B.
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