Total Synthesis of the 7,10-Epimer of the Proposed Structure of Amphidinolide N, Part II: Synthesis of C17-C29 Subunit and Completion of the Synthesis-Reference-Cited by-同舟云学术

Total Synthesis of the 7,10-Epimer of the Proposed Structure of Amphidinolide N, Part II: Synthesis of C17-C29 Subunit and Completion of the Synthesis

Published:2016-02-04 Issue:10 Volume:22 Page:3287-3291
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Ochiai Koji¹,Kuppusamy Sankar¹,Yasui Yusuke¹,Harada Kenji¹,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

Reference45 articles.

1. Chem. Eur. J 2016 22

2. Directed reduction of .beta.-hydroxy ketones employing tetramethylammonium triacetoxyborohydride

3. The directed reduction of β-hydroxy ketones employing Me4NHB(OAc)3

4. Lewis acid-mediated condensation of alkenols and aldehydes. A selective synthesis of tetrahydropyrans and oxepanes

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