Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103108
Title: A synthesis of 5-hydroxysedamine using hydroformylation
Authors: Bates, Roderick Wayland
Nur Filza Mohamed Aslam
Tang, Chi H.
Simon, Oliver
Keywords: Science::Chemistry::Organic chemistry::Organic synthesis
Issue Date: 2014
Source: Bates, R. W., Nur Filza Mohamed Aslam, Tang, C. H., & Simon, O. (2014). A synthesis of 5-hydroxysedamine using hydroformylation. Tetrahedron, 70(12), 2134-2140.
Journal: Tetrahedron
Series/Report no.: Tetrahedron
Abstract: A synthesis of 5-hydroxysedamine, a Sedum alkaloid, has been completed using N,O-heterocycle chemistry to establish the aminoalcohol structure, hydroformylation to form the piperidine ring and diastereoselective dihydroxylation to introduce the 5-hydroxy group.
URI: https://hdl.handle.net/10356/103108
http://hdl.handle.net/10220/24359
ISSN: 0040-4020
DOI: 10.1016/j.tet.2014.02.001
Schools: School of Physical and Mathematical Sciences 
Rights: © 2014 Elsevier Ltd. This is the author created version of a work that has been peer reviewed and accepted for publication by Tetrahedron, Elsevier Ltd. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [Article DOI: http://dx.doi.org/10.1016/j.tet.2014.02.001].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

Files in This Item:
File Description SizeFormat 
A Synthesis of 5-Hydroxysedamine using Hydroformylation.pdfMain article181.55 kBAdobe PDFThumbnail
View/Open

SCOPUSTM   
Citations 20

11
Updated on Mar 16, 2025

Web of ScienceTM
Citations 20

10
Updated on Oct 31, 2023

Page view(s) 50

652
Updated on Mar 27, 2025

Download(s) 20

301
Updated on Mar 27, 2025

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.