Computation-Assisted Structural Elucidation of Epoxyroussoeone and Epoxyroussoedione Isolated from Roussoella japanensis KT1651-Reference-Cited by-同舟云学术

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Computation-Assisted Structural Elucidation of Epoxyroussoeone and Epoxyroussoedione Isolated from Roussoella japanensis KT1651

Published:2015-06-25 Issue:7 Volume:78 Page:1505-1510
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Honmura Yuna¹,Takekawa Hiroto¹,Tanaka Kazuaki¹,Maeda Hayato¹,Nehira Tatsuo²,Hehre Warren³,Hashimoto Masaru¹

Affiliation:

1. Faculty of Agriculture and Bioscience, Hirosaki University, 3-Bunkyo-cho, Hirosaki, Aomori 036-8561, Japan

2. Graduate School of Integrated Arts and Sciences, Hiroshima University, 1-7-1, Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8521, Japan

3. Wavefunction, Inc., 18401 Von Karman Avenue, Suite 370, Irvine, California 92612, United States

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/np500924n

Reference20 articles.

1. Walking in the woods with quantum chemistry – applications of quantum chemical calculations in natural products research

2. Successful combination of computationally inexpensive GIAO 13C NMR calculations and artificial neural network pattern recognition: a new strategy for simple and rapid detection of structural misassignments

3. Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability

4. Quantum Mechanical Calculation of NMR Parameters in the Stereostructural Determination of Natural Products

5. The Assignment of Absolute Stereostructures through Quantum Chemical Circular Dichroism Calculations

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1. Highly Functionalized Spirobisnaphthalenes from Roussoella sp. KT4147;Journal of Natural Products;2024-07-17

2. Five new aromatic polyketides and isoquinoline alkaloids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021;Tetrahedron;2022-11

3. Enantioselective Synthesis of Spiro‐oxiranes: An Asymmetric Addition/Aldol/Spirocyclization Domino Cascade;Angewandte Chemie International Edition;2021-08-18

4. Enantioselective Synthesis of Spiro‐oxiranes: An Asymmetric Addition/Aldol/Spirocyclization Domino Cascade;Angewandte Chemie;2021-08-18

5. 2-Oxaspiro[4.5]decane and α-pyrenocine derivatives from the endophytic fungus Roussoella sp. PSU-H51;Natural Product Research;2021-04-14

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