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Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C

Ya-Mu Xia 1
Ya-Mu Xia
Liang Chang 1
Liang Chang
Yining Ding 1
Yining Ding
Bin Jiao 1
Bin Jiao
Published 2010-05-06
CommunicationVolume 20, Issue 3, 151-152
3
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Xia Y. et al. Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C // Mendeleev Communications. 2010. Vol. 20. No. 3. pp. 151-152.
GOST all authors (up to 50) Copy
Xia Y., Chang L., Ding Y., Jiao B. Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C // Mendeleev Communications. 2010. Vol. 20. No. 3. pp. 151-152.
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TY - JOUR
DO - 10.1016/j.mencom.2010.05.009
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.009
TI - Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C
T2 - Mendeleev Communications
AU - Xia, Ya-Mu
AU - Chang, Liang
AU - Ding, Yining
AU - Jiao, Bin
PY - 2010
DA - 2010/05/06
PB - Mendeleev Communications
SP - 151-152
IS - 3
VL - 20
ER -
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@article{2010_Xia,
author = {Ya-Mu Xia and Liang Chang and Yining Ding and Bin Jiao},
title = {Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C},
journal = {Mendeleev Communications},
year = {2010},
volume = {20},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.009},
number = {3},
pages = {151--152},
doi = {10.1016/j.mencom.2010.05.009}
}
MLA
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MLA Copy
Xia, Ya-Mu, et al. “Asymmetric synthesis of erythro-8-O-4’-neolignan Machilin C.” Mendeleev Communications, vol. 20, no. 3, May. 2010, pp. 151-152. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.009.

Keywords

Marchilin C; Neolignans; Asymmetric synthesis

Abstract

A new methodology for the synthesis of the erythro-8-O-4’-neolignan Machilin C based on the Sharpless asymmetric dihydroxylation reaction and the Mitsunobu reaction as two key steps is described.

References

1.
Lignans from machilus thunbergii
Shimomura H., Sashida Y., Oohara M.
Phytochemistry, 1987
2.
Lignans, neolignans, and related compounds.
Ward R.S.
Natural Product Reports, 1999
3.
10.1016/j.mencom.2010.05.009_bib3
Mei
J. Org. Chem., 2009
4.
Lignans and Neolignans from Brassica fruticulosa:  Effects on Seed Germination and Plant Growth
Cutillo F., D'Abrosca B., DellaGreca M., Fiorentino A., Zarrelli A.
Journal of Agricultural and Food Chemistry, 2003
5.
Antimalarial Compounds from Rhaphidophora decursiva
Zhang H., Tamez P.A., Hoang V.D., Tan G.T., Hung N.V., Xuan L.T., Huong L.M., Cuong N.M., Thao D.T., Soejarto D.D., Fong H.H., Pezzuto J.M.
Journal of Natural Products, 2001
7.
Anti-leishmanial activity of neolignans from Virola species and synthetic analogues
Barata L.E., Santos L.S., Ferri P.H., Phillipson J.D., Paine A., Croft S.L.
Phytochemistry, 2000
10.
Streamlined, Asymmetric Synthesis of 8,4‘-Oxyneolignans
Curti C., Zanardi F., Battistini L., Sartori A., Rassu G., Pinna L., Casiraghi G.
Journal of Organic Chemistry, 2006
12.
Phenomenon of Optical Self-Purification of Chiral Non-Racemic Compounds
Soloshonok V.A., Ueki H., Yasumoto M., Mekala S., Hirschi J.S., Singleton D.A.
Journal of the American Chemical Society, 2007
13.
The Osmium-Catalyzed Asymmetric Dihydroxylation: A New Ligand Class and a Process Improvement
Sharpless K.B., Amberg W., Bennani Y.L., Crispino G.A., Hartung J., Jeong K.S., Kwong H.L., Morikawa K., Wang Z.M.
Journal of Organic Chemistry, 1992