Structural Reassignment of Two Polyenol Natural Products-Reference-Cited by-同舟云学术

Structural Reassignment of Two Polyenol Natural Products

Published:2023-02-03 Issue:9 Volume:26 Page:
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur J Org Chem

Author:

Kutateladze Andrei G.¹^ORCID,Bates Roderick W.²^ORCID,Elyashberg Mikhail³^ORCID,Williams Craig M.⁴^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry University of Denver Denver CO 80208 USA

2. School of Chemistry Chemical Engineering and Biotechnology Nanyang Technological University 21 Nanyang Link Singapore 637371 Singapore

3. Advanced Chemistry Development Inc. (ACD/Labs) Toronto ON M5 C 1B5 Canada

4. School of Chemistry and Molecular Biosciences University of Queensland Brisbane 4072 Queensland Australia

Abstract

AbstractUnusual polyenols that defied chemical principles were reassigned as the nucleosides, adenosine and uridine, using a combination of chemical intuition underpinned by Computer Assisted Structure Elucidation (CASE) and DFT methods.

Funder

University of Denver

University of Queensland

Nanyang Technological University

Australian Research Council

National Science Foundation

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202201316

Reference18 articles.

1. Alkenes with antioxidative activities from Murraya koenigii (L.) Spreng

2. Secondary metabolites from an endophytic fungus Trichoderma erinaceum with antimicrobial activity towards Pythium ultimum

3. Chasing Molecules That Were Never There: Misassigned Natural Products and the Role of Chemical Synthesis in Modern Structure Elucidation

4. Structural revisions of natural products by total synthesis

5. Survey of marine natural product structure revisions: A synergy of spectroscopy and chemical synthesis

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