Total Synthesis of Hoiamide A Using an Evans–Tishchenko Reaction as a Key Step-Reference-Cited by-同舟云学术

Total Synthesis of Hoiamide A Using an Evans–Tishchenko Reaction as a Key Step

Published:2019-07-05 Issue:14 Volume:21 Page:5471-5474
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Guo Yian¹^ORCID,Zhou Jingjing¹,Gao Bowen¹,Zhao Meng¹,Yan Jia-Lei¹,Xu Zhengshuang¹,Choi Sun¹²^ORCID,Ye Tao¹³^ORCID

Affiliation:

1. State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Genomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China

2. College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, Korea

3. Tsinghua University Shenzhen Graduate School, Xili, Nanshan District, Shenzhen 518055, China

Funder

National Research Foundation of Korea

China Postdoctoral Science Foundation

Natural Science Foundation of Guangdong Province

National Natural Science Foundation of China

Shenzhen Science and Technology Innovation Committee

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b01735

Reference32 articles.

1. Hoiamide A, a Sodium Channel Activator of Unusual Architecture from a Consortium of Two Papua New Guinea Cyanobacteria

2. The Hoiamides, Structurally Intriguing Neurotoxic Lipopeptides from Papua New Guinea Marine Cyanobacteria

3. Hoiamide D, a marine cyanobacteria-derived inhibitor of p53/MDM2 interaction

4. Involvement of JNK and Caspase Activation in Hoiamide A-Induced Neurotoxicity in Neocortical Neurons

5. Discovery of Amantamide, a Selective CXCR7 Agonist from Marine Cyanobacteria

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