338 0

Full metadata record

DC FieldValueLanguage
dc.contributor.advisor조천규-
dc.contributor.author송지영-
dc.date.accessioned2017-11-29T02:30:33Z-
dc.date.available2017-11-29T02:30:33Z-
dc.date.issued2017-08-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/33727-
dc.identifier.urihttp://hanyang.dcollection.net/common/orgView/200000431098en_US
dc.description.abstractErythrina alkaloids in the pea famliy widely distributed in the vegetable field consist of about 70 kinds of natural products and have interesting azatetracyclic structures (A, B, C, D) in common. They represent an attractive synthetic target substance for pharmacological effects including sedation, hypotension, neuromuscular blockade, and CNS activity. An erythrina alkaloid [(±)-Erysotramidine, (±)-Erysotrine, (±)-Erythramine, (±)-Erythraline] was synthesized to further expand the 2-pyrone strategy for target-directed synthesis. Here we report the strategic use of our 3,5-dibromo-2-pyrone and Diels-Alder reactions for the total synthesis of erythrina alkaloids.-
dc.publisher한양대학교-
dc.titleTotal Synthesis of Alkaloid Natural Products Starting with 3,5-Dibromo-2-pyrone as a Useful Building Block-
dc.title.alternative유용한 빌딩 블록으로써 출발물질인 3,5-다이브로모파이론을 통한 천연물의 전합성: 에리스리나 알칼로이드의 전합성-
dc.typeTheses-
dc.contributor.googleauthor송지영-
dc.contributor.alternativeauthorJiyoung Song-
dc.sector.campusS-
dc.sector.daehak대학원-
dc.sector.department화학과-
dc.description.degreeDoctor-
Appears in Collections:
GRADUATE SCHOOL[S](대학원) > THEATER & FILM(연극영화학과) > Theses (Master)
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE