Enantioselective synthesis of R-(−)-ligularenolide starting from S-(+)-carvone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Ligularenolide. A new sesquiterpene lactone of eremophilane type
2. The structure of ligularenolide
3. PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum. I. Taxonomy of Producing Strain, Fermentation, Isolation and Biological Activities.
4. PF1092A, B and C, New Nonsteroidal Progesterone Receptor Ligands Produced by Penicillium oblatum. II. Physico-chemical Properties and Structure Elucidation.
5. Synthesis of (.+-.)-PF1092A, B, and C; New Nonsteroidal Progesterone Receptor Ligands.
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1. Ozonolytic transformations of ( R )‐(−)‐carvon in the presence of pyridine;Journal of the Chinese Chemical Society;2022-03
2. Total Synthesis of the Sesquiterpenoid Periconianone A Based on a Postulated Biogenesis;J AM CHEM SOC;2017
3. Effect of three 2-allyl-p-mentha-6,8-dien-2-ols on inhibition of mild steel corrosion in 1M HCl;Arabian Journal of Chemistry;2014-11
4. ChemInform Abstract: Enantioselective Synthesis of R-(-)-Ligularenolide Starting from S-(+)-Carvone.;ChemInform;2010-06-24
5. Nucleophilic Additions to Dienes, Enynes and Polyenes;PATAI'S Chemistry of Functional Groups;2009-12-15
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