Biomimetic Asymmetric Total Synthesis of (−)-Laurefucin via an Organoselenium-Mediated Intramolecular Hydroxyetherification-Reference-Cited by-同舟云学术

Biomimetic Asymmetric Total Synthesis of (−)-Laurefucin via an Organoselenium-Mediated Intramolecular Hydroxyetherification

Published:2008-11-17 Issue:49 Volume:130 Page:16807-16811
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kim Byungsook¹,Lee Miseon¹,Kim Mi Jung¹,Lee Hyunjoo¹,Kim Sanghee¹,Kim Deukjoon¹,Koh Minseob¹,Park Seung Bum¹,Shin Kye Jung¹

Affiliation:

1. The Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 151-742, Korea, Department of Chemistry, Seoul National University, Seoul 151-747, Korea, and Life Sciences Research Division, Center for Chemoinformatics Research, Korea Institute of Science and Technology, Seoul 130-650, Korea

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja806304s

Reference53 articles.

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2. Metabolites of the red alga Laurencia subopposita

3. The Structure of Notoryne, a Halogenated C15Nonterpenoid with a Novel Carbon Skeleton from the Red AlgaLaurenda nipponicaYamada

4. New C15 Acetogenins and Sesquiterpenes from the Red Alga Laurencia sp. cf. L. gracilis

5. The revised structure and absolute configuration of laurefucin from Yamada

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