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Cited 8 time in webofscience Cited 8 time in scopus
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Total Synthesis of Gramistilbenoids A, B, and C

Authors
Harmalkar, Dipesh S.Lu, QiliLee, Kyeong
Issue Date
Apr-2018
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF NATURAL PRODUCTS, v.81, no.4, pp 798 - 805
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
JOURNAL OF NATURAL PRODUCTS
Volume
81
Number
4
Start Page
798
End Page
805
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/9616
DOI
10.1021/acs.jnatprod.7b00865
ISSN
0163-3864
1520-6025
Abstract
Stilbenes are biologically active metabolites of plants that have the potential to attenuate a broad range of human diseases. Gramistilbenoids are a class of natural products with a stilbene skeleton, isolated from the bamboo orchid (Arundina graminifolia), and with significant cytotoxicity against cancer cell lines (NB4, A549, SHSYSY, PC3, and MCF7). These are the first identified naturally occurring diphenylethylenes to possess a hydroxyethyl unit. However, some of these compounds are not abundant in nature, and thus, their synthesis is advantageous. This paper reports the first synthesis of gramistilbenoids A (1), B (2), and C (3), with overall yields of 10, 2, and 8% respectively. These natural products were synthesized using key reactions, such as Horner-Wadsworth-Emmons olefination, Stille coupling, and hydroboration oxidation.
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