Enantioselective Total Syntheses of (+)-Hostmanin A, (−)-Linderol A, (+)-Methyllinderatin and Structural Reassignment of Adunctin E-Reference-Cited by-同舟云学术

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Enantioselective Total Syntheses of (+)-Hostmanin A, (−)-Linderol A, (+)-Methyllinderatin and Structural Reassignment of Adunctin E

Published:2015-04-17 Issue:9 Volume:80 Page:4526-4531
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dethe Dattatraya H.¹,Dherange Balu D.¹

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur-208016, India

Funder

Department of Science and Technology, Ministry of Science and Technology

Council of Scientific and Industrial Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b00331

Reference42 articles.

1. New Monoterpene-Substituted Dihydrochalcones fromPiper aduncum

2. Two flavonoids from two Lindera umbellata varieties

3. A novel hexahydrodibenzofuran derivative with potent inhibitory activity on melanin biosynthesis of cultured B-16 melanoma cells from Lindera umbellata bark.

4. Activity-guided isolation of antiplasmodial dihydrochalcones and flavanones from Piper hostmannianum var. berbicense

5. The First Total Synthesis of (±)-Linderol A, a Tricyclic Hexahydrodibenzofuran Constituent of Lindera umbellata Bark, with Potent Inhibitory Activity on Melanin Biosynthesis of Cultured B-16 Melanoma Cells

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