Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricus-Reference-Cited by-同舟云学术

Elucidation of Relative and Absolute Configurations of Highly Rearranged Diterpenoids and Evidence for a Putative Biosynthetic Intermediate from the Australian Nudibranch Goniobranchus geometricus

Published:2018-11-12 Issue:3 Volume:82 Page:449-455
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Forster Louise C.¹,Pierens Gregory K.²,Garson Mary J.¹^ORCID

Affiliation:

1. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia

2. Centre for Advanced Imaging, The University of Queensland, Brisbane, QLD 4072, Australia

Funder

Australia and Pacific Science Foundation

School of Chemistry and Molecular Biosciences, University of Queensland

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.8b00713

Reference37 articles.

1. Determination of Relative Configuration in Organic Compounds by NMR Spectroscopy and Computational Methods

2. Stereochemical Determination of Acyclic Structures Based on Carbon−Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products

3. Minimalist Relativistic Force Field: Prediction of Proton–Proton Coupling Constants in 1H NMR Spectra Is Perfected with NBO Hybridization Parameters

4. Cytotoxic Spiroepoxide Lactone and Its Putative Biosynthetic Precursor from Goniobranchus Splendidus

5. A guide to small-molecule structure assignment through computation of (1H and 13C) NMR chemical shifts

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