Stereoselective Construction of 2,7-Disubstituted fused-Bis Tetrahydrofuran Skeletons: Biomimetic-Type Synthesis and Biological Evaluation of (±)- and (−)-Aplysiallene and Their Derivatives-Reference-Cited by-同舟云学术

Stereoselective Construction of 2,7-Disubstituted fused-Bis Tetrahydrofuran Skeletons: Biomimetic-Type Synthesis and Biological Evaluation of (±)- and (−)-Aplysiallene and Their Derivatives

Published:2015-10-07 Issue:20 Volume:80 Page:10261-10277
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Yamakawa Maki¹,Kurachi Takeshi¹,Yoshikawa Yusuke¹,Arisawa Mitsuhiro¹,Okino Yuichiro²,Suzuki Kuniaki²,Fujioka Hiromichi¹

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565-0871, Japan

2. Graduate School of Dental Medicine, Hokkaido University, Kita-13 Nishi-7, Kitaku, Sapporo, Hokkaido 060-8586, Japan

Funder

Uehara Memorial Foundation

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01882

Reference40 articles.

1. A c-15 non-terpenoid from the red alga Laurencia okamurai

2. Aplysiallene, a New Bromoallene as an Na, K-ATPase Inhibitor from the Sea Hare, Aplysia kurodai

3. Omaezallene from Red AlgaLaurenciasp.: Structure Elucidation, Total Synthesis, and Antifouling Activity

4. Structures of Halogenated Chamigrene Derivatives, Minor Constituents from the Red AlgaLaurencia nipponicaYamadan

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

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