Evidence map›Paper›PMID 34704367›Full record

ArticleChemistry, an Asian journal2022

Asymmetric Total Syntheses, Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol A.

Kento Nishikibe, Keisuke Nishikawa, Momochika Kumagai, Matsumi Doe, Yoshiki Morimoto

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kento NishikibeDepartment of Chemistry, Graduate School of Science, Osaka City University Sumiyoshi-ku, Osaka, 558-8585, Japan.
Keisuke NishikawaDepartment of Chemistry, Graduate School of Science, Osaka City University Sumiyoshi-ku, Osaka, 558-8585, Japan.ORCID http://orcid.org/0000-0002-3170-8023
Momochika KumagaiDepartment of Chemistry, Graduate School of Science, Osaka City University Sumiyoshi-ku, Osaka, 558-8585, Japan.ORCID http://orcid.org/0000-0002-5631-3167
Matsumi DoeDepartment of Chemistry, Graduate School of Science, Osaka City University Sumiyoshi-ku, Osaka, 558-8585, Japan.
Yoshiki MorimotoDepartment of Chemistry, Graduate School of Science, Osaka City University Sumiyoshi-ku, Osaka, 558-8585, Japan.ORCID http://orcid.org/0000-0002-4770-3091

Funding

Nagase Science Technology FoundationSasakawa Scientific Research Grant from the Japan Science SocietySuntory Foundation for Life Sciences Bioorganic Research Institute
6 · The paper itself

Abstract

There are marine cytotoxic bromotriterpenoids, named the thyrsiferol family that are structurally characterized by some tetrahydropyran (THP) and tetrahydrofuran (THF) rings. The thyrsiferol family belongs to natural products that are often difficult to determine their stereostructures even by the current, highly advanced spectroscopic methods, especially in acyclic systems including stereogenic tetrasubstituted carbon centers. In such cases, it is effective to predict and synthesize the possible stereostructures. Herein, to elucidate ambiguous stereostructures and unassigned absolute configurations of aplysiol B, laurenmariannol, and saiyacenol A, members of the thyrsiferol family, we carried out their asymmetric chemical syntheses featuring 6-exo and 5-exo oxacyclizations of epoxy alcohol precursors and 6-endo bromoetherification of a bishomoallylic alcohol. In this paper, we report total assignments of their stereostructures through their asymmetric chemical syntheses and also their preliminary cytotoxic activities against some tumor cells. These results could not have been achieved without depending on asymmetric total synthesis.

Indexed as

configuration determinationcytotoxicitynatural productsstructure elucidationtotal synthesis

Identifiers

PMID34704367
PMCPMC9299038

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.