Total Synthesis and Stereochemical Revision of Iriomoteolide-2a-Reference-Cited by-同舟云学术

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Total Synthesis and Stereochemical Revision of Iriomoteolide-2a

Published:2018-02-27 Issue:14 Volume:57 Page:3801-3805
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Sakamoto Keita¹²,Hakamata Akihiro²,Tsuda Masashi³,Fuwa Haruhiko¹^ORCID

Affiliation:

1. Department of Applied Chemistry; Faculty of Science and Engineering; Chuo University, 1-13-27 Kasuga; Bunkyo-ku Tokyo 112-8551 Japan

2. Graduate School of Life Sciences; Tohoku University; 2-1-1 Katahira Aoba-ku Sendai 980-8577 Japan

3. Center for Advanced Marine Core Research and Department of Agriculture and Marine Science; Kochi University; Nankoku Kochi 783-8502 Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Sumitomo Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference49 articles.

1. Amphidinolides and Its Related Macrolides from Marine Dinoflagellates

2. Iriomoteolide-2a, a Cytotoxic 23-Membered Macrolide from Marine Benthic Dinoflagellate Amphidinium Species

3. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids

4. Application of Modified Mosher's Method for Primary Alcohols with a Methyl Group at C2 Position.

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