Total Synthesis of the 7,10-Epimer of the Proposed Structure of Amphidinolide N, Part I: Synthesis of the C1-C13 Subunit-Reference-Cited by-同舟云学术

Total Synthesis of the 7,10-Epimer of the Proposed Structure of Amphidinolide N, Part I: Synthesis of the C1-C13 Subunit

Published:2016-02-04 Issue:10 Volume:22 Page:3282-3286
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Ochiai Koji¹,Kuppusamy Sankar¹,Yasui Yusuke¹,Okano Tsubasa¹,Matsumoto Yasunobu¹,Gupta Nishant R.¹,Takahashi Yohei²,Kubota Takaaki²³,Kobayashi Jun'ichi²,Hayashi Yujiro¹⁴

Affiliation:

1. Department of Industrial Chemistry; Faculty of Engineering; Tokyo University of Science; Kagurazaka, Shinjuku-ku Tokyo 162-8601 Japan

2. Graduate School of Pharmaceutical Sciences; Hokkaido University; Sapporo 060-0812 Japan

3. Showa Pharmaceutical University; 3-3165 Higashi-Tamagawagakuen, Machida Tokyo 194-8543 Japan

4. Department of Chemistry; Graduate School of Science; Tohoku University; Aoba-ku Sendai 980-8578 Japan

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference58 articles.

1. Amphidinolide N, a novel 26-membered macrolide with remarkably potent cytotoxicity from the cultured marine dinoflagellate Amphidinium sp.

2. Diastereoselective Formation of Tetrahydrofurans via Pd-Catalyzed Asymmetric Allylic Alkylation: Synthesis of the C13–C29 Subunit of Amphidinolide N

3. Revised structure and stereochemical assignments of amphidinolide N

4. Synthesis of iso-epoxy-amphidinolide N and des-epoxy-caribenolide I structures. Revised strategy and final stages

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