Bark extractives of Catalpa bungei: isolation, purification and structural elucidation of triterpene, phytosterol and flavonoid derivatives-Reference-Cited by-同舟云学术

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Bark extractives of Catalpa bungei: isolation, purification and structural elucidation of triterpene, phytosterol and flavonoid derivatives

Published:2020-11-04 Issue:1 Volume:55 Page:231-241
ISSN:0043-7719
Container-title:Wood Science and Technology
language:en
Short-container-title:Wood Sci Technol

Author:

Xu Jiayun,Lu Nan,Liu Kun,Liu Huayu,Wang Zhi,Bae Youngsoo,Si Chuan-Ling^ORCID,Wang Junhui

Funder

National Basic Research Program of China

Key Technology Research and Development Program of Tianjin

Tianjin Enterprise Technology Commissioner Project

Publisher

Springer Science and Business Media LLC

Subject

Industrial and Manufacturing Engineering,Plant Science,General Materials Science,Forestry

Link

http://link.springer.com/content/pdf/10.1007/s00226-020-01239-5.pdf

Reference30 articles.

1. Agrawal PK (1989) Carbon-13 NMR of flavonoids. Elsevier, New York

2. Bitchi MB, Magid AA, Yao-Kouassi PA, Kabran FA, Harakat D, Martinez A, Morjani H, Tonzibo FZ, Voutquenne-Nazabadioko L (2019) Triterpene saponins from the roots of Parkia bicolor A. Chev Fitoter 137:104264. https://doi.org/10.1016/j.fitote.2019.104264

3. Collins FW, Bruceand AB, Cornelius KW (1975) Flavonol glycoside gallates from Tellima grandiflora. Phytochemistry 14(4):1099–1102. https://doi.org/10.1016/0031-9422(75)85195-8

4. Delgado MCC, Silva MSD, Fo RB (1984) 3β-hydroxy-21β-e-cinnamoyloxyolean-12-en-28-oic acid, a triterpenoid from enterolobium contorstisiliquum. Phytochemistry 23:2289–2292. https://doi.org/10.1016/S0031-9422(00)80537-3

5. Forgo P, Kövér KE (2004) Gradient enhanced selective experiments in the 1H NMR chemical shift assignment of the skeleton and side-chain resonances of stigmasterol, a phytosterol derivative. Steroids 69:43–50. https://doi.org/10.1016/j.steroids.2003.09.012

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