The Journal of Organic Chemistry · 2015 · 22 citations · 55 references
Natural SciencesChemistryMedicinal ChemistryOrganic ChemistrySynthetic Medicinal ChemistryDiversity-oriented SynthesisHeterocycle SynthesisHeterocyclic ChemistryMacrocycle SynthesisRadical ReactionsRetrosynthetic AnalysisNatural Product Total SynthesisRadical CyclizationRing-forming Reactions
Making use of a tandem free radical cyclization process mediated by Mn(OAc)3 as a key operation, the total synthesis of retrojusticidin B, justicidin E, and helioxanthin has been concisely achieved in four or five steps in an overall yield of 45, 33 and 44%, respectively, from a common starting material 5.
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Lignans, neolignans and related compounds
Robert S. Ward · Natural Product Reports · 1999 · 357 citations
Rulong Yan, Jia Luo, Chuanxin Wang et al. · The Journal of Organic Chemistry · 2010 · 163 citations · Full text
Chi-Chih Chang, Mong‐Wei Lin, Shoei‐Sheng Lee et al. · Antiviral Research · 1995 · 133 citations