Access count of this item: 9
|Title:||Formal Total Synthesis of (±)-Strictamine Based on a Gold-Catalyzed Cyclization|
|Author's alias:||大石, 真也|
|Publisher:||American Chemical Society|
|Journal title:||Organic Letters|
|Abstract:||A gold-catalyzed cyclization of 1-propargyl-1, 2, 3, 4-tetrahydro-β-carboline led to formation the D-ring of strictamine. Functional group modifications of the resulting tetracyclic indolenine led to the formal total synthesis of (±)-strictamine.|
|Rights:||This document is the Accepted Manuscript version of a Published Work that appeared in final form in 'Organic Letters', copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.6b00536.|
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|Appears in Collections:||Journal Articles|
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