Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A

Date

Authors

Schwartz, Brett

Jones, Matthew

Banwell, Martin

Cade, Ian

Publisher

American Chemical Society

Abstract

The synthesis of the enantiomer of the structure, 1, assigned to the natural product nobilisitine A has been accomplished using the enantiomerically pure cis-1,2-dihydrocatechol 4 as starting material. The1H and13C NMR spectral data derived from compound

Keywords

Keywords: alkaloid; biological product; fused heterocyclic rings; nobilisitine A; angiosperm; article; chemical structure; chemistry; nuclear magnetic resonance; stereoisomerism; synthesis; Alkaloids; Biological Products; Heterocyclic Compounds with 4 or More Rings

URI

http://hdl.handle.net/1885/57860

Collections

ANU Research Publications

Source

Organic Letters

Type

Journal article

DOI

10.1021/ol102249q

Restricted until

2037-12-31

Downloads

File

Description

01_Schwartz_Synthesis_of_the_enantiomer_of_2010.pdf (256.25 KB)