A rapid construction of the ABC tricyclic skeleton of malabanone A
Author:
Affiliation:
1. State Key Laboratory of Applied Organic Chemistry
2. College of Chemistry and Chemical Engineering
3. Lanzhou University
4. Lanzhou
5. P. R. China
Abstract
The ABC tricyclic skeleton of malabanone A was accomplished in a concise route starting from R-carvone.
Funder
National Natural Science Foundation of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02495B
Reference23 articles.
1. Malabanones A and B, novel nortriterpenoids from Ailanthus malabarica DC
2. Concise Total Synthesis of Isospongian Diterpenoid (±)-Polyrhaphin D
3. Rapid construction of the 6/6/5 tricyclic framework via a tandem radical cyclization reaction and its application to the synthesis of 5-epi-7-deoxy-isoabietenin A
4. Total synthesis of (−)-8-epi-chromazonarol enabled by a unique N2H4·H2O promoted intramolecular oxa-Michael cyclization reaction
5. A novel limonoid from the seeds of Chisocheton siamensis
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