First total synthesis of Mappain with a Prenylated and Gernylated Stilbene

Title
First total synthesis of Mappain with a Prenylated and Gernylated Stilbene
Author(s)
이용록락코즈 차크라파니[락코즈 차크라파니]정은미[정은미]
Keywords
RESVERATROL OLIGOMERS; OLIGOSTILBENES; PICEATANNOL; ANALOGS; COMPLEX; PLANT
Issue Date
201005
Publisher
WILEY-BLACKWELL
Citation
HELVETICA CHIMICA ACTA, v.93, no.5, pp.829 - 836
Abstract
The first synthesis of naturally occuring mappain has been achieved by a convergent sequence. The key strategy involved in the synthesis of mappain was a (E)-stilbene formation by Horner-Wads-worth-Emmons reation of the corresponding prenylated benzaldehyde with a geranylated benzyl phosphonate.
URI
http://hdl.handle.net/YU.REPOSITORY/22455
ISSN
0018-019X
Appears in Collections:
공과대학 > 화학공학부 > Articles
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