An Asymmetric Total Synthesis of Broussonetine C
Author:
Affiliation:
1. a School of Chemistry , Monash University , P.O. Box 23, Victoria , 3800 , Australia
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1081/CAR-120026470
Reference14 articles.
1. Studies on the Constituents of Broussonetia Species. I. Two New Pyrrolidine Alkaloids, Broussonetines C and D, as .BETA.-Galactosidase and .BETA.-Mannosidase Inhibitors from Broussonetia kazinoki SIEB.
2. Studies on the Constituents of Broussonetia Species. II. Six New Pyrrolidine Alkaloids, Broussonetine A, B, E, F and Broussonetinine A and B, as Inhibitors of Glycosidases from Broussonetia kazinoki SIEB.
3. First total synthesis of a new tetrasubstituted pyrrolidine alkaloid, broussonetine C
4. Copper-catalysed coupling of undec-10-enylmagnesium bromide with ω-functionalised halogenoalkanes as a key reaction for the synthesis of novel bipolar phospholipids with different head groups and chain length
5. The reduction of benzylidene derivatives of pentose diethyl dithioacetals with lithium aluminium hydride-aluminium trichloride
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