Synthesis of the C19 methyl ether of aspercyclide A via germyl-Stille macrocyclisation and ELISA evaluation of both enantiomers following optical resolution.
File(s)Spivey, A - Synthesis of the C19 Methyl Ether.pdf (772.67 KB) Spivey, A - Synthesis of the C19 Methyl Ether (ESI).pdf (1.61 MB)
Accepted version
Supporting information
Author(s)
Type
Journal Article
Abstract
Aspercyclide A (1) is a biaryl ether containing 11-membered macrocyclic natural product antagonist of the human IgE-FcεRI protein-protein interaction (PPI); a key interaction in the signal transduction pathway for allergic disorders such as asthma. Herein we report a novel approach to the synthesis of the C19 methyl ether of aspercyclide A, employing a Pd(0)-catalysed, fluorous-tagged alkenylgermane/arylbromide macrocyclisation (germyl-Stille reaction) as the key step, and evaluation of both enantiomers of this compound via ELISA following optical resolution by CSP-HPLC. A crystal structure for germyl hydride 27 is also reported.
Date Issued
2011-10-07
Citation
Org Biomol Chem, 2011, 9 (19), pp.6814-6824
ISSN
1477-0520
Publisher
ROYAL SOC CHEMISTRY
Start Page
6814
End Page
6824
Journal / Book Title
Org Biomol Chem
Volume
9
Issue
19
Copyright Statement
© The Royal Society of Chemistry 2011
Description
20.08.12 KB. Accepted version, ok to add, embargo period as expired (accepted 4 Jul 11). RSC policy
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000294720600051&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Subjects
Chemistry Techniques, Synthetic
Chromatography, High Pressure Liquid
Crystallography, X-Ray
Cyclization
Enzyme-Linked Immunosorbent Assay
Lactones
Macrocyclic Compounds
Methyl Ethers
Models, Molecular
Molecular Structure
Stereoisomerism
Notes
PubMed ID: 21845261
Coverage Spatial
England