Literature DB >> 23725829

Determination of the absolute configuration of natural products.

Ling-Yi Kong1, Peng Wang.   

Abstract

Structural elucidation of natural products is always one of the most important tasks for natural product researchers in related fields. Particularly, the absolute configuration (AC), being a great challenge for natural product chemists, has attracted much attention. During the past few decades, many techniques and approaches have been developed to determine the AC of natural products, including direct (or absolute) methods, e.g. X-ray diffraction (XRD), electronic and vibrational circular dichroism (ECD and VCD), and Raman optical activity (ROA), as well as indirect (or relative) methods using a reference or a derivatizing agent with known AC, e.g. CD with empirical rules and nuclear magnetic resonance (NMR) utilizing anisotropic effects of chiral derivatizing agents. However, none of the currently applied techniques is capable of dominating AC determination, since they each have their respective limitations corresponding to the different structural features. This mini review summarizes most of the techniques and methods which are commonly used in AC assignment of natural products, or have potential application prospects, and briefly describes their principles, advantages and limitations.
Copyright © 2013 China Pharmaceutical University. Published by Elsevier B.V. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23725829     DOI: 10.1016/S1875-5364(13)60016-3

Source DB:  PubMed          Journal:  Chin J Nat Med        ISSN: 1875-5364


  7 in total

1.  New Techniques of Structure Elucidation for Sesquiterpenes.

Authors:  Julio C Pardo-Novoa; Carlos M Cerda-García-Rojas
Journal:  Prog Chem Org Nat Prod       Date:  2021

2.  A Novel Antioxidant Protects Against Contrast Medium-Induced Acute Kidney Injury in Rats.

Authors:  Shuo Huang; Yanyan Tang; Tianjun Liu; Ning Zhang; Xueyan Yang; Dingwei Yang; Ge Hong
Journal:  Front Pharmacol       Date:  2020-11-27       Impact factor: 5.810

3.  NP-MRD: the Natural Products Magnetic Resonance Database.

Authors:  David S Wishart; Zinat Sayeeda; Zachary Budinski; AnChi Guo; Brian L Lee; Mark Berjanskii; Manoj Rout; Harrison Peters; Raynard Dizon; Robert Mah; Claudia Torres-Calzada; Mickel Hiebert-Giesbrecht; Dorna Varshavi; Dorsa Varshavi; Eponine Oler; Dana Allen; Xuan Cao; Vasuk Gautam; Andrew Maras; Ella F Poynton; Pegah Tavangar; Vera Yang; Jeffrey A van Santen; Rajarshi Ghosh; Saurav Sarma; Eleanor Knutson; Victoria Sullivan; Amy M Jystad; Ryan Renslow; Lloyd W Sumner; Roger G Linington; John R Cort
Journal:  Nucleic Acids Res       Date:  2022-01-07       Impact factor: 16.971

4.  Cycloelatanene A and B: absolute configuration determination and structural revision by the crystalline sponge method.

Authors:  Shoukou Lee; Manabu Hoshino; Makoto Fujita; Sylvia Urban
Journal:  Chem Sci       Date:  2016-10-27       Impact factor: 9.825

5.  Cytotoxic Serrulatane-Type Diterpenoids from the Gorgonian Euplexaura sp. and Their Absolute Configurations by Vibrational Circular Dichroism.

Authors:  Fei Cao; Chang-Lun Shao; Yun-Feng Liu; Hua-Jie Zhu; Chang-Yun Wang
Journal:  Sci Rep       Date:  2017-10-02       Impact factor: 4.379

6.  Meliacarpinin-Type Limonoids from the Bark of Melia toosendan.

Authors:  Yalin Hu; Li Heng; Rong Xu; Junhe Li; Shanshan Wei; Deran Xu; Jun Luo; Yi Li
Journal:  Molecules       Date:  2018-10-10       Impact factor: 4.411

7.  Absolute Configuration Assignment to Chiral Natural Products by Biphenyl Chiroptical Probes: The Case of the Phytotoxins Colletochlorin A and Agropyrenol.

Authors:  Ernesto Santoro; Stefania Vergura; Patrizia Scafato; Sandra Belviso; Marco Masi; Antonio Evidente; Stefano Superchi
Journal:  J Nat Prod       Date:  2020-02-24       Impact factor: 4.050

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.