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Synthesis of all four stereoisomers of 5-hydroxy-4-methyl-3-heptanone using plants and oyster mushrooms

Date

Authors

Bohman, Bjorn

Unelius, C.R.

Publisher

Elsevier

Abstract

All four possible stereoisomers of 5-hydroxy-4-methyl-3-heptanone were synthesized from common achiral reagents using fast, straightforward organic synthesis, including the use of whole tissue of Daucus carota, Solanum melongena, and Pleurotus ostreatus.

Keywords

Keywords: 5 hydroxy 4 methyl 3 heptanone; heptane derivative; hydroxyl group; methyl group; unclassified drug; article; aubergine; carbon nuclear magnetic resonance; carrot; drug synthesis; enantioselectivity; nonhuman; Pleurotus ostreatus; priority journal; proton Enantioselective, ß-Hydroxyketone; Mushrooms; Plants; Sitophilure

URI

http://hdl.handle.net/1885/63743

Collections

ANU Research Publications

Source

Tetrahedron

Type

Journal article

DOI

10.1016/j.tet.2009.08.049

Restricted until

2037-12-31

Downloads

File

Description

01_Bohman_Synthesis_of_all_four_2009.pdf (197.04 KB)