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.

The enantioselective synthesis of APTO and AETD: polyhydroxylated β-amino acid constituents of the microsclerodermin cyclic peptides

Date

Authors

Shuter, Emily C

Duong, Hung

Hutton, Craig A

McLeod, Malcolm

Publisher

Royal Society of Chemistry

Abstract

The polyhydroxylated β-amino acids (2S,3R,4S,5S,7E)-3-amino-8-phenyl- 2,4,5-trihydroxyoct-7-enoic acid (APTO) and (2S,3R,4S,5S,7E,9E)-3-amino-10-(4- ethoxyphenyl)-2,4,5-trihydroxydeca-7,9-dienoic acid (AETD) are key components of the microsclerodermin fa

Keywords

Keywords: AETD; Aminohydroxylation; APTO; Microsclerodermin cyclic peptides; Aldehydes; Amino acids; Enantioselectivity; Fungus protection; Stereochemistry; Synthesis (chemical); Peptides; cyclopeptide; microsclerodermin E; unclassified drug; article; stereoisomeri

URI

http://hdl.handle.net/1885/52698

Collections

ANU Research Publications

Source

Organic and Biomolecular Chemistry

Type

Journal article

DOI

10.1039/b707891a

Restricted until

2037-12-31

Downloads

File

Description

01_Shuter_The_enantioselective_synthesis_2007.pdf (200.85 KB)