Concise Syntheses of Hyrtioreticulins C and D via a C-4 Pictet–Spengler Reaction: Revised Signs of Specific Rotations-Reference-Cited by-同舟云学术

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Concise Syntheses of Hyrtioreticulins C and D via a C-4 Pictet–Spengler Reaction: Revised Signs of Specific Rotations

Published:2017-01-30 Issue:2 Volume:80 Page:241-245
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Abe Takumi¹^ORCID,Yamada Koji¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-tobetsu, Hokkaido 0610293, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.7b00008

Reference67 articles.

1. Hyrtioreticulins A–E, indole alkaloids inhibiting the ubiquitin-activating enzyme, from the marine sponge Hyrtios reticulatus

2. Hyrtioerectines A−C, Cytotoxic Alkaloids from the Red Sea Sponge Hyrtios erectus

3. Reticulatins A and B and hyrtioreticulin F from the marine sponge Hyrtios reticulatus

4. The Pictet-Spengler Reaction in Nature and in Organic Chemistry

5. Strictosidine Synthase: Mechanism of a Pictet−Spengler Catalyzing Enzyme

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