Complete sets of descriptors for the prediction of 13 C NMR chemical shifts of quinoline derivatives-Reference-Cited by-同舟云学术

Complete sets of descriptors for the prediction of 13 C NMR chemical shifts of quinoline derivatives

Published:2018-12-16 Issue:3 Volume:33 Page:e3107
ISSN:0886-9383
Container-title:Journal of Chemometrics
language:en
Short-container-title:Journal of Chemometrics

Author:

Yu Xinliang¹²^ORCID,Dang Limin¹^ORCID

Affiliation:

1. Hunan Provincial Key Laboratory of Environmental Catalysis & Waste Regeneration, College of Chemistry and Chemical EngineeringHunan Institute of Engineering Xiangtan China

2. State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical EngineeringHunan University Changsha China

Funder

Open Project Program of State Key Laboratory of Chemo/Biosensing and Chemometrics (Hunan University

Scientific Research Fund of Hunan Provincial Education Department

Publisher

Wiley

Subject

Applied Mathematics,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cem.3107

Reference28 articles.

1. Descriptor Selection Methods in Quantitative Structure–Activity Relationship Studies: A Review Study

2. The Importance of Being Earnest: Validation is the Absolute Essential for Successful Application and Interpretation of QSPR Models

3. Backbone and side-chain 1H, 15N, and 13C resonance assignments of a novel Staphylococcal inhibitor of myeloperoxidase

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

5. Determination of the geometry of acetoxyendiynes and acetoxyenynes by NMR heteronuclear 13C1H scalar couplings and 13C NMR chemical shifts. Structural assignment of the oxylipin natural products peyssonenynes A and B

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