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The Structure of the Lycorenine Alkaloid Nobilisitine A

Date

Authors

Schwartz, Brett

White, Lorenzo

Banwell, Martin

Willis, Anthony

Publisher

American Chemical Society

Abstract

The structure 3 recently proposed, on the basis of computed NMR chemical shifts, for the natural product nobilisitine A has been synthesized from its C5-epimer (+)-clividine (4). The spectral data derived from compound 3 match those reported for the natural product.

Keywords

Keywords: Natural products; NMR chemical shifts; Spectral data; Amaryllidaceae alkaloid; lycorinine alkaloid; nobilisitine A; unclassified drug; article; carbon nuclear magnetic resonance; chemical reaction; chemical structure; diastereoisomer; epimer; fragmentatio

URI

http://hdl.handle.net/1885/60295

Collections

ANU Research Publications

Source

Journal of Organic Chemistry

Type

Journal article

DOI

10.1021/jo2016899

Restricted until

2037-12-31

Downloads

File

Description

01_Schwartz_The_Structure_of_the_2011.pdf (817.41 KB)